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  • Articles: DFG German National Licenses  (289)
  • 1980-1984  (289)
  • 1981  (172)
  • 1980  (117)
  • Molecular Cell Biology  (221)
  • Life Sciences  (169)
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  • Articles: DFG German National Licenses  (289)
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  • 1980-1984  (289)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981) 
    ISSN: 0275-3723
    Keywords: Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 15-27 
    ISSN: 0275-3723
    Keywords: epidermal growth factor ; epidermal growth factor receptor ; integral membrane proteins ; hormone receptor ; limited proteolysis ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Microsomal membranes from human placenta, which bind 5-20 pmol of 125I-epidermal growth factor (EGF) per mg protein, have been affinity-labeled with 125I-EGF either spontaneously or with dimethylsuberimidate. Coomassie blue staining patterns on SDS polyacrylamide gels are minimally altered, and the EGF-receptor complex appears as a specifically labeled band of 180,000 daltons which is not removed by urea, neutral buffers, or chaotropic salts but is partially extracted by mild detergents. Limited proteolysis by alpha chymotrypsin and several other serine proteases yields labeled fragments of 170,000, 130,000, 85,000, and 48,000 daltons. More facile cleavage by papain or bromelain rapidly degrades the hormone-receptor complex to smaller labeled fragments of about 35,000 and 25,000 daltons. These fragments retain the binding site for EGF, are capable of binding EGF, and remain associated with the membrane. Alpha chymotryptic digestion of receptor solubilized by detergents yields the same fragments obtained with intact vesicles, suggesting that the fragments may represent intrinsic proteolytic domains of the receptor.
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 317-326 
    ISSN: 0275-3723
    Keywords: culture substratum ; influence on morphogenesis ; mouse hepatoma ; phenotypes in vitro ; surface antigens ; modulation by culture substratum; ; tumor malignancy in vivo ; modification by preculture ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: We have found that a murine hepatoma displays a considerable phenotypic diversification in culture, which depends upon the substratum utilized, and is manifested by the formation of multicellular structures of differing geometry: Monolayer on glass and plastic, thick multilayer pads on Gelfilm, and spheroids on agar and agarose. These multicellular morphological phenotypes were assayed without disruption to ascertain their antigenicity in vitro and their tumorigenicity in vivo and to obtain quantitative information on the effect of the spatial arrangement of the hepatoma cells upon the ability of each multicellular structure to interact, as a whole, with molecules and cells in its surroundings.The antigenicity of the multicellular structures was determined with calibrated probes and a methodology that measures the total antigenicity, as well as antigenicity per unit of surface area. Antigenicity was found to differ in the following decreasing order: Monolayer on plastic 〉 spheroids on agarose 〉 spheroids on agar 〉 multilayer on Gelfilm. At least part of these antigenic variants arise from different degrees of masking of the structures' surface determinants by a trypsin-sensitive material.The multicellular phenotypes also differed in tumorigenicity. When assayed in syngeneic hosts under comparable conditions, agar-grown spheroids produced the fewest tumors, whereas Gelfilm-grown multilayers produced the most.These two independent sets of data show that the various geometries that a tumor tissue is induced to acquire by the culture substratum are accompanied by a distinctive combination of surface and biological properties.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 395-402 
    ISSN: 0275-3723
    Keywords: lectins (vertebrate) ; heparin ; Glycosaminoglycans ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Extracts of young rat lung contain a heparin-inhibitable lectin that closely resembles one recently purified from chicken liver. Both lectins interact with heparin and N-acetyl-D-galactosamine, and were purified by gel filtration on Sepharose CL-2B followed by affinity chromatography on heparin-Sepharose. They both behave as high molecular weight aggregates that can be dissociated into two peptides with apparent molecular weights of 13,000 and 16,000 by gel electrophoresis in SDS. Samples of purified lectin contained up to 20% DNA by weight, and the degree of lectin aggregation and hemagglutination activity was greatly reduced by treatment with micrococcal nuclease without inhibiting heparin-binding activity. Association of lectin with DNA is an artifact of homogenization in high salt, since only 2% of the lectin is found associated with a purified nuclear fraction.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 16 (1981), S. 1-13 
    ISSN: 0275-3723
    Keywords: DNA polymerasc α ; nuclear DNA/protein complex ; SV40 T-antigen ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: A nuclear DNA complex containing DNA polymerase and SV40 T-antigen was isolated from nuclei of SV40-transformed mouse fibroblasts. DNA polymerase could be separated from the complex. The remaining DNA/T-antigen-containing complex stimulated DNA polymerase a activity about 10-fold. The complex contained 4 major proteins with molecular weights of 46, 54, 76, and 94 kilodalton (KD). The stimulation activity was retained by protein A-Sepharose loaded with specific IgG from SV40-tumor bearer serum, or from antisera against the 94 KD and 76 KD components and was partially inhibited in the presence of these antisera. The stimulation activity was completely abolished by treatment of the complex with trypsin or DNase I.
    Additional Material: 3 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 16 (1981), S. 15-27 
    ISSN: 0275-3723
    Keywords: limb bud ; Fab inhibition ; Ca++ dependence ; specificity ; trypsin sensitivity ; immunological analysis ; cell surface antigen ; cerebellum ; chick embryo ; retina ; heart ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: We have investigated the adhesive properties of cells from several neural and nonneural chick embryonic tissues dissociated using modifications of the standard dissociation procedures employed routinely in this laboratory to obtain retinal cells. Each of these tissues (7-day optic tectum, retina, and heart, and 3.75-day hmb bud) displayed both Ca++-dependent (CD) and Ca++-independent (CI) aggregation, the relative rates of which differed from tissue to tissue In every case, cells prepared so as to display one mode of aggregation or the other cross-adhered readily to cells - regardless of tissue origin - displaying the same mode of aggregation. Cross adhesion was negligible between cells - even from the same tissue - prepared so as to display different modes of aggregation. Anti-retinal Fab molecules which inhibit selectively either the CI or CD aggregation of retina cells strongly inhibited the corresponding aggregation of optic tectum cells, but had no effect upon the aggregation (CI or CD) of heart cells. These results demonstrate the exis-tence in the tissues examined of dual adhesion mechanisms similar in Ca++ dependence and recognition properties to those of the retina, but showing certain immunological distinctions from the latter. The imrmunological relationship among the adhesion mechanisms from the various tissues is under continuing investigation.
    Additional Material: 11 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 16 (1981), S. 91-103 
    ISSN: 0275-3723
    Keywords: DNA repair ; DNA glycosylases ; E coli ; AP endonucleases ; UV radiation ; alkylation damage ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: This brief review presents the salient features of new developments in the enzymatic repair of base damage to DNA. DNA glycosylases and apurinic/ apyrimidinic (AP) endonucleases are reviewed and evidence is presented that in at least two prokaryote systems incision of UV-irradiated DNA occurs by the sequential action of these two classes of enzymes. In contradistinction, the uvrA, uvrB, and uvrC gene products of E coli appear to function as a multiprotein complex that catalyzes hydrolysis of phosphodiester bonds in damaged DNA directly. The inducible rapid repair of O6- methylguanine in E coli is also reviewed.
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 16 (1981), S. 105-113 
    ISSN: 0275-3723
    Keywords: hormone receptors ; diphtheria toxin ; lysosomes ; hybrid proteins ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Recently we have isolated six variants of Swiss/3T3 mouse fibroblasts that are resistant to the cytotoxic insulin-diphtheria toxin A fragment. All of the variants proved to have greatly reduced or no insulin binding capacity, and several variants showed altered morphologies and growth characteristics. We now report on the further characterization of one of these variants, CI-3. which displays a massive accumulation of membranous vesicles in its cytoplasm. By electron microscopy these vesicles resemble lysosomes. They also appear to fluorcsce bright orange after treatment of viable cells with acridine orange. However, the specific activity of several lysosomal enzymes is depressed in CI-3. Additionally, there is an apparent shift in the density of vesicles containing lysosomal enzymes in this variant. These alterations may be directly related to CI-3′s resistance to the cytotoxic insulin and have some important bearings on the mechanism of insulin action.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 16 (1981), S. 133-138 
    ISSN: 0275-3723
    Keywords: trifoliin A ; clover lectin ; Rhizobium trifolii ; root exudate ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Trifoliin A, a Rhizobium-binding glycoprotein from white clover, was detected in sterile clover root exudate by a sensitive immunofluorescence assay employing encapsulated cells of Rhizobium trifolii 0403 heat-fixed to microscope slides. Its presence in root exudate was further examined by immunoaffinity chromatography. The binding of trifoliin A to cells was specifically inhibited by the hapten, 2-deoxyglucose. Significantly higher quantities of trifoliin A were detected in root exudate of seedlings grown hydroponically in nitrogen-free medium than in rooting medium containing 15 mM NO-3, a concentration which completely suppressed root hair infection by the nitrogen-fixing symbiont. The presence of trifoliin A in root exudate may make it possible for recognition processes to occur before the microsymbiont attaches to its plant host.
    Additional Material: 2 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 16 (1981), S. 167-177 
    ISSN: 0275-3723
    Keywords: gene duplication ; H-2 alloantigen ; Qa-2 alloanligen ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The region of the murine 17th chromosome telomeric to H-2D encodes a group of serologically defined cell surface antigens termed Qa-1-5. These antigens are of interest because their expression is restricted to hematopoietic cells. In addition, the molecular weight and subunit structure (ie, association with β-2 microglobulin) of Qa-2 molecules are similar to H-2 and TL antigens. In the present studies, we have prepared isotopically labeled Qa-2 and H-2 molecules from mitogen-stimulated C57BL/6 spleen cells. Comparative peptide mapping of tryptic peptides from Qa-2 and H-2 molecules (Kb, DbKk, Dd) reveal that Qa-2 has a unique primary structure. However, considerable homology is indicated since 30-40% of the Qa-2 peptides cochromatograph with peptides derived from H-2Kb, H-2Db, H-2Kk, and H-2Dd. Studies by other investigators have demonstrated that similar levels of structural homology are observed when H-2K, H-2D, and H-2L tryptic peptides are analyzed. We conclude from these studies that the Qa-2 alloantigen is structurally related to a class of cell surface molecules (ie, H-2) that play critical roles in immune recognition processes. These data further suggest that the genes encoding Qa-2 and H-2 molecules have arisen from a common primordial gene.
    Additional Material: 4 Ill.
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  • 11
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 16 (1981), S. 193-207 
    ISSN: 0275-3723
    Keywords: recombinant DNA ; acute leukemia virus ; bacleriophage λ ; R-looping ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Avian myelocytomatosis virus (MC29), a defective acute leukemia virus, has a broad oncogenic spectrum in vivo, and transforms fibroblasts and hematopoietic target cells in vitro. We have used recombinant DNA technology to isolate and characterize the sequences that are essential in the transformation process. Integrated MC29 proviral DNA was isolated from a library of recombinant phage containing DNA from the MC29-transformed nonproducer quail cell line Q5. The cloned DNA was analyzed by Southern blotting of restriction endonuclease digests and by electron microscopic visualization of R-loops formed between the cloned DNA and MC29 or helper virus RNA. It was found that the 9.2 kb cloned DNA insert contains approximately 4 kb of viral sequences and 5.2 kb of quail cellular sequences. The viral sequences contain all of the MC29-specific sequences and 5′ helper related sequences as well as part of the envelope region. The size of the cloned EcoRI fragment is the same as that of the major band in EcoRI-cleaved Q5 DNA that hybridizes to viral sequences. Transfection of the cloned DNA into NIH 3T3 cells revealed that the MC29-specific sequences are functional in that they induce foci of trans-formed cells with high efficiency.
    Additional Material: 7 Ill.
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 16 (1981), S. 233-242 
    ISSN: 0275-3723
    Keywords: lectins ; slime mold lectins ; vertebrate lectins ; chicken-lactose-lectin-I ; chicken-lactose-lectin-II ; chicken heparin lectin ; Dictyostelium ; secretion ; muscle development ; extracellular materials ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Endogenous lectins in both cellular slime molds and chicken tissues have been localized primarily intracellularly, in contrast with the predominantly extracellular localization of the glycoproteins, glycolipids, and glycosaminoglycans with which they might interact. Here we present evidence that lectins in both of these organisms may be externalized and become associated with the cell surface and/or extracellular materials. In chicken intestine, chicken-lactose-lectin-II is shown to be localized in the secretory granules of the goblet cells, along with mucin, and to be secreted onto the intestinal surface. In embryonic muscle, chicken-lactose-lectin-I is shown to be externalized with differentiation, ultimately becoming localized on the surface of myotubes and in the extracellular spaces. In a cellular slime mold, Dictyostelium purpureum, externalization of lectin is elicited by either polyvalent glycoproteins that bind the small amount of endogenous cell surface lectin, or by slime mold or plant lectins that bind unoccupied complementary cell surface oligosaccharides. These results suggest that externalization of endogenous lectin may be a response to specific external signals. We conclude that lectins are frequently held in intracellular reserves awaiting release for specific external functions.
    Additional Material: 3 Ill.
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  • 13
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 16 (1981) 
    ISSN: 0275-3723
    Keywords: Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 16 (1981), S. 303-309 
    ISSN: 0275-3723
    Keywords: bleomycin ; DNA repair ; human DNA repair defects ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The ability of human fibroblasts to repair bleomycin-damaged DNA was examined in vivo. Repair of the specific lesions caused by bleomycin (BLM) was investigated in normal cell strains as well as those isolated from patients with apparent DNA repair defects. The diseases ataxia telangiectasia (AT), Bloom syndrome (BS), Cockayne syndrome (CS), Fanconi anemia (FA), and xeroderma pigmentosum (XP) were those selected for study. The method used for studying the repair of DNA after BLM exposure was alkaline sucrose gradient centrifugation. After exposure to BLM, a fall in the molecular weight of DNA was observed, and after drug removal the DNA reformed rapidly to high molecular weight. The fall in molecular weight upon exposure to BLM was observed in all cells examined with the exception of some XP strains. Prelabeled cells from some XP complementation groups were found to have a higher percentage of low molecular weight DNA on alkaline gradients than did normal cells. This prelabeled low molecular weight DNA disappeared upon exposure to BLM.
    Additional Material: 2 Ill.
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 16 (1981), S. 385-392 
    ISSN: 0275-3723
    Keywords: fibronectin ; intestinal epithelial cell adhesion ; laminin ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Rabbit intestinal epithelial cells, obtained after a limited hyaluronidase digestion, were incubated in medium with or without calf serum, on bacteriological plastic dishes. The dishes, either plain or coated with an air-dried type I collagen film, were pretreated with medium alone or with medium containing purified laminin or purified fibronectin. Cells did not attach in significant numbers to untreated bacteriological plastic, even in the presence of serum. Cells did attach to collagen-coated dishes, and were judged viable on the basis of their incorporation of radiolabeled leucine into cell protein. Cell adhesion to the collagen substrate increased in proportion to the concentration of serum in the medium, with maximal attachment at 5% serum or greater. Pretreatment of plain or collagen-coated dishes with increasing amounts of fibronectin enhanced cell adhesion in a concentration-dependent manner. Either serum, or fibronectin-free serum in the medium enhanced cell attachment to substrates pretreated with cither fibronectin or laminin. Thus, intestinal epithelial cells appear to possess surface receptors for both laminin and fibronectin. The evidence further suggests that calf serum may contain factors, other than fibronectin, capable of enhancing intestinal epithelial cell attachment to collagen substrates.
    Additional Material: 6 Ill.
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  • 16
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 17 (1981), S. 79-86 
    ISSN: 0275-3723
    Keywords: neurite outgrowth ; neuron survival ; weaver mouse ; cerebellar cultures ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: In the present study we report for the first time a weaver (wv) gene dose effect on neuron survival and neurite formation in vitro. Dissociated cerebellar cells from postnatal 7- and 8-day-old normal ( + / + ), heterozygous weaver ( + /wv) and homozygous weaver (wv/wv) mice were cultured as monolayers on poly-L-lysine coated glass. Cell death occurred rapidly in wv/wv cultures. Cell counts showed that less than 20% of the total neurons and neuronal precursors (identified by “birthday” radiolabeling techniques) survived by Day 3. Cell death was less extensive in + /wv cultures with 65% of the total neurons and 80% of the precursors surviving by Day 3. In contrast to wv/wv cultures, younger neurons survive better than the total population in + /wv cultures. The impairment of neurite formation over the first week is also proportional to the number of mutant genes as shown by quantitation of (a) the percentage of cells with neurites; (b) the percentage of cells with neurites of a given length class with time; (c) the lengths of the longest processes formed per cell. The mean longest neurite lengths obtained by computer digitization at 6 days in vitro were 41.8, 26.8, and 9.0 μm for + / +, + /wv, and wv/wv granule cells, respectively.
    Additional Material: 4 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 17 (1981), S. 69-77 
    ISSN: 0275-3723
    Keywords: human breast epithelia ; glycoproteins ; proteinase inhibitors ; organ culture ; α-1-antichymotrypsin ; breast adenocarcinoma ; glandular structure ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The synthesis and release of glycoproteins were studied in organ cultures of human breast surgical specimens and in established breast epithelial cell lines, MCF-7 and MDA-MB-231. Biosynthesis was monitored by the incorporation of 14C-glucosamine. Labeled macromolecules in the culture supernatants were analyzed by biochemical and immunological techniques. One to 8% of the labeled glycoproteins from benign breast and infiltrating ductal carcinoma specimens was precipitated by antibodies produced against human serum 7α-1-antichymotrypsin. Twelve percent of the total glycoproteins from the culture supernatants of the MCF-7 cell line was identified as α-1-antichymo-trypsin. Both the normal serum and the human breast epithelia-derived proteinase inhibitor can be resolved into similar subclasses by two-dimensional gel electrophoresis. MDA-MB-231 and MCF-7 cells which were extensively washed with EDTA, serum-free medium, and phosphate-buffered saline retain this proteinase inhibitor on their cell surfaces. Three to 4% of the total cell-surface iodinated components was immunoprecipitated by these specific antibodies. Since α-1-antichymotrypsin is a potent inhibitor of neutral proteinases such as cathepsin G, the demonstration of its synthesis by benign and malignant breast epithelial cells is of considerable interest. This glycoprotein may represent the epithelia's own protective shield of cell surface components and the cell's attempt to moderate the effects of invading leukocytes. In addition, it may play a regulatory role in the maintenance of three-dimensional glandular structures.
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 17 (1981), S. 99-120 
    ISSN: 0275-3723
    Keywords: Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Additional Material: 7 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 17 (1981), S. 163-181 
    ISSN: 0275-3723
    Keywords: spectrin-actin complex ; membranoskeleton ; immunoelectron microscopy ; membrane remodeling ; endocytosis ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The mature mammalian erythrocyte has a unique membranoskeleton, the spectrin-actin complex, which is responsible for many of the unusual membrane properties of the erythrocyte. Previous studies have shown that in successive stages of differentiation of the erythropoietic series leading to the mature erythrocyte there is a progressive increase in the density of spectrin associated with the membranes of these cells. An important stage of this progression occurs during the enucleation of the late erythroblast to produce the incipient reticulocyte, when all of the spectrin of the former cell is sequestered to the membrane of the reticulocyte. The reticulocyte itself, however, does not exhibit a fully formed membranoskeleton. In particular, the in vitro binding of multivalent ligands to specific membrane receptors on the reticulocyte was shown to cause a clustering of some fractions of these ligand-receptor complexes into special mobile domains on the cell surface. These domains of clustered ligand-receptor complexes became invaginated and endocytosed as small vesicles. By immunoelectron microscopic experiments, these invaginations and endocytosed vesicles were found to be specifically free of spectrin on their cytoplasmic surfaces.These earlier findings then raised the possibility that the maturation of reticulocytes to mature erythrocytes in vivo might involve a progressive loss of reticulocyte membrane free of spectrin, thereby producing a still more concentrated spectrin-actin membranoskeleton in the erythrocyte than in the reticulocyte. This proposal is tested experimentally in this paper. In vivo reticulocytes were observed in ultrathin frozen sections of spleens from rabbits rendered anemic by phenylhydrazine treatment. These sections were indirectly immunolabeled with ferritin-antibody reagents directed to rabbit spectrin. Most reticulocytes in a section had one or more surface invaginations and one or more intra-cellular vesicles that were devoid of spectrin labeling. The erythrocytes in the same sections did not exhibit these features, and their membranes were everywhere uniformly labeled for spectrin. Spectrin-free surface invaginations and intracellular vesicle were also observed with reticulocytes within normal rabbit spleens. Based on these results, a scheme for membrane remodeling during reticulocyte maturation in vivo is proposed.
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  • 20
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 17 (1981), S. 223-230 
    ISSN: 0275-3723
    Keywords: β-galactoside lectin ; galaptin ; erythropoiesis ; murine erythroleukemia cells (MELC) ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Recently, the generic term “galaptins” was proposed for the group of low molecular weight, acidic, β-galactoside-specific protein lectins that have been isolated from a wide variety of animal tissues and are thought to have a role in cell-cell recognition and adhesion. A molecule of this type, called erythroid developmental agglutinin (EDA), has been isolated from rabbit bone marow where it seems to mediate the intererythroblast adhesion seen in erythroblastic islands during erythropoiesis in vivo. Here, we show that after purification, EDA shows 95%-100% Coomassie blue staining as a single component on electrophoresis in native, urea, and SDS polyacrylamide gels and electrofocuses as a single band at pH 5.6. EDA has a subunit molecular weight of 13,000 in SDS gels and, unlike the majority of other galaptins, which arc dimeric, native EDA is monomeric in solution. Another monomeric galaptin, chicken lactose lectin II, has been described recently, and it therefore seems that there may be two classes of galaptin distinguishable by their aggregation state in solution.We have previously reported that EDA agglutinates rabbit erythroblasts in vitro and that this reaction is inhibited by β-galactoside-containing sugars and by anti-EDA Fab fragments suggesting that EDA bridges directly between cell surface glycoproteins. The insensitivity of this reaction to cooling, or to the disruption of cellular metabolism or the cytoskeleton demonstrated here further supports this hypothesis. EDA-mediated erythroblast agglutination was also shown to be independent of divalent cations.Since galaptins are thought to be important in cohesion between normal cells, the possibility that EDA is not active in leukemic erythroid tissue was examined. The murine erythroleukemia cell line (MELC) provided an excellent system for this study since MELC are thought to be derived from an erythroid committed cell transformed at an early stage of development and can be induced by a number of chemical agents to differentiate terminally along the erythroid developmental pathway in culture. EDA of rabbit origin was found to agglutinate mouse erythroblasts in vitro and was used to investigate the response of MELC to EDA. It was found that the transformed cells were not readily agglutinated by EDA but on induction, and the concomitant loss of many of their transformed characteristics, MELC gained aggregation competence for EDA. The possible causes of these differences are discussed.
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  • 21
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 17 (1981), S. 245-257 
    ISSN: 0275-3723
    Keywords: tumor promotion ; carcinogenesis ; epidermal cells ; 12-0-teradecanolylphorbol-13-acetate (TPA) ; terminal differentiation ; initiation ; transglutaminase ; ornithine decarboxylase ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Mouse epidermal basal cells can be selectively cultivated in medium with a calcium concentration of 0.02-0.09 mM. Terminal differentiation and slouching of mature kcratinocytes occur when the calcium concentration is increased to 1.2-1.4 mM. When basal cell cultures are exposed to chemical initiators of carcinogenesis, colonies of cells that resist calcium-induced differentiation evolve. Likewise, basal cells derived from mouse skin initiated in vivo yield foci that resist terminal differentiation. This defect in the commitment to terminal differentiation appears to be an essential change in initiated cells in skin and is also characteristic of malignant epidermal cells. This model system has also provided a means to determine if basal cells are more responsive to phorbol esters than other cells in epidermis and to explore the possibility that heterogeneity of response exists within subpopulations of basal cells. The induction of the enzyme ornithine decarboxylase (ODC) was used as a marker for responsiveness to phorbol esters. ODC induction after exposure to 12-0-tetradccanoylphorbol-13-acetate (TPA) in basal cells is enhanced 20-fold over the response of a culture population containing both differentiating and basal cells. When basal cells are induced to differentiate by increased calcium, responsiveness to TPA is lost within several hours. In basal cell cultures, two ODC responses can be distinguished. After exposure to low concentrations of TPA or to weak promoters of the phorbol ester series, ODC activity is maximal at 3 hr. With higher concentrations of TPA, the ODC maximum is at 9 hr. These results arc consistent with the presence of subpopulations of basal cells with differing sensitivities to TPA. Other studies that use the enzyme epidermal transglutaminase as a marker for differentiation support this conclusion. In basal cell culture TPA exposure rapidly increases transglutaminase activity and cornified envelope development, reflecting induced differentiation in some cells. As differentiated cells arc sloughed from the dish, the remaining basal cells proliferate and become resitant to induced differentiation by 1.2 m M calcium. These data provide additional evidence of basal cell heterogeneity in which TPA induces one subpopulation to differentiate while another is stimulated to proliferate and resists a differentiation signal. Tumor promoters, by their ability to produce heterogeneous responses with regard to terminal differentiation and proliferation, would cause redistribution of subpopulations of epidermal cells in skin. Cells that resist signals for terminal differentiation, such as initiated cell, would be expected to increase in number during remodeling. Clonal expansion of the intitiated population could result in a benign tumor with an altered program of differentiation. In skin, benign tumors are the principal product of 2-stage carcinogenesis. Subsequent progression to malignancy may involve an additional step, probably a genetic alteration, that is independent of the tumor promoter.
    Additional Material: 2 Ill.
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  • 22
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 17 (1981), S. 313-324 
    ISSN: 0275-3723
    Keywords: Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 23
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 17 (1981), S. 347-357 
    ISSN: 0275-3723
    Keywords: myeloid progenitor cells ; bone marrow ; stroma ; manosaccharides ; colony-stimulating factor ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Adherent stromal cells from mouse bone marrow inhibited the formation of granulocyte/monocyte (G/M) colonies induced in vitro by colony-stimulating factor (CSF), This inhibition occurred both when crude conditioned media obtained from various sources were used to induce colony formation or when a pure CSF preparation from mouse lung origin was tested. The inhibition did not appear to be toxic in nature since despite the lack of colony formation, progenitor CFU-C proliferated in the presence of stromal cells. Medium conditioned by adherent stromal cells was devoid of inhibitory activity when incorporated into the culture medium used for G/M colony formation, indicating that the inhibitory activity may not be present in a soluble form. Inhibitors of prostaglandins did not affect G/M colony formation. In contrast, D-glucose and a number of other free monosaccharides but not pyruvate lactate or glycerol induced formation fo myeloid colonies in the presence of stromal cells. This did not require addition of exogenous CSF. Released factors concentrated from serum-free medium conditioned by stromal cells exhibited colony-stimulating activity provided that the medium contained a high glucose concentration during incubation. It is proposed that stromal cells produce a resident CSF that, in contrast to exogenous CSF species, is capable of inducing myelopoiesis within the bone marrow stroma.
    Additional Material: 3 Ill.
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  • 24
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 17 (1981), S. 359-368 
    ISSN: 0275-3723
    Keywords: developmental regulation of glycoprotein ; glycoprotein biosynthesis ; during life-cycle D discoideum ; in D discoideum ; assembly of glycoproteins during development ; regulation of glycoproteins during development ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: We have examined the glycoprotein-linked oligosaccharides assembled during the life cycle of Dictyostelium discoideum, and found their expression to be dramatically dependent upon the stage of development. During early development mature glycans have a high mannose character, and a substantial proportion acquire a fucose residue that correlates with endo-H resistance. One-third of the glycans also acquire sulfate residues. These glycans diminish in importance during aggregation.The mature glycans expressed during late development contain fewer mannose residues, from five to ten mannose residues, and are characterized by the absence of sulfate residues and by the presence of fucose residues on endo-H-sensitive glycans. These glycans make their appearance coincident with the construction of tips on tight cell mounds. At this stage glycans characteristic of both early and late stages occur simultaneously.Developmental regulation of the wide array of protein-linked glycans expressed during the life cycle of Dictyostelium discoideum may be as simple as the controlled transition from a group of structures that are assembled by the vegetative cells to a group of structures that are assembled by the terminally differentiating cells. The potential biological significance of this transition is discussed.
    Additional Material: 4 Ill.
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  • 25
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 17 (1981), S. 99-146 
    ISSN: 0275-3723
    Keywords: Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Type of Medium: Electronic Resource
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  • 26
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 17 (1981), S. 319-351 
    ISSN: 0275-3723
    Keywords: Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Type of Medium: Electronic Resource
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  • 27
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: A schematic representation of the variety of products which can be obtained by microbial conversion of cellulose is presented.Alkaline pre-treatment has been used after milling in all the experiments. Solka-floc or sugarcane bagasse was used as sources of cellulose. A cellulolytic strain of Aspergillus terreus (ATCC 30514) was cultivated in batch-, fed batch and continuous culture up to 7 liter stirred tank fermenter. The general growth characteristics were determined by growing on glucose. Results of experiments on the growth of A. terreus for production of biomass on Solka-floc or Sugarcane bagasse are given, also the ability of crude cellulases to produce sugar syrups by enzymatic hydrolysis of cellulose has been evaluated.
    Additional Material: 5 Tab.
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  • 28
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 207-246 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
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  • 29
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Examination show how far the stirred tank fermenter meets the requirements of multi-phase systems under conditions of microbiological protein synthesis. 1The homogeneity attained by mixing of 4-phase-fermentation medium will be influenced by different amounts of material flow of the correspondent process conditions.2Limitation of nitrogen and solved nutrient - and trace salts in culture liquid by unsatisfactorily mixing can be excluded. The solute-oxygen concentration and homogeneous distribution of solute-oxygen in the culture liquid are influencing the economy of fermentation.3The homogeneity concerning petroleum distillate-, biomass-and air distribution highly depends from biomass content of the fermentation medium.
    Additional Material: 21 Ill.
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  • 30
    Electronic Resource
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 279-284 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Lipids were extracted from the cells of Lodderomyces elongisporus EH 15 grown on gas oil (Bp. 240 to 360 °C) with benzine/alcohol (80:20). The lipid-hydrocarbon-fraction obtained by this extraction method was 18.5%. It was composed of hydrocarbons, phospholipids, fatty acids, glycerides, sterols, ubiquinones, and vitamines. The main components among the lipids were phospholipids. The compositions of phospholipid, fatty acid, sterol, and ubiquinone fractions were analysed.
    Additional Material: 4 Ill.
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  • 31
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 32
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: A brief review of the most important properties and fields of application of microbial proteinases are presented. Special possibilities of an industrial utilization of these enzymes are discussed: in the photographic industry for the production and degradation of gelatin as well as for silverless photography, in the food industry for the improvement of the functional properties of proteins as well as for increasing their nutritive value, in organic synthesis for the production of peptides, and in sewage treatment plants for the stabilization of sludge.
    Additional Material: 7 Ill.
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  • 33
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The influence of the carbon substrates glucose and methanol on enzyme activities of the yeast Candida methylica was investigated by substrate-shift experiments in discontinuous cultivation. Growth on glucose results in a repression of the enzymes necessary for methanol utilization. After depletion of glucose or addition of methanol these enzymes are derepressed or induced, respectively. Changes in the activity of enzymes of the intermediary metabolism turn out differently both in intensity and direction as a result of substrate-shifts. The results suggest a basic change in the metabolism by growing Candida methylica in glucose or methanol.
    Additional Material: 2 Ill.
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  • 34
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 191-195 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract in Russian.
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  • 35
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 201-204 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 36
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
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  • 37
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Coordinated regulation of carbon and energetic metabolism enzymes is characteristic of lysine producing strains of Brevibacterium flavum. ATP is the regulating effector and changes in the stationary ATP-concentration in cells cause certain alternations of enzyme activities in the basic metabolism pathways. The goal of the experiments was the use of the biochemical regulations of methabolism in order to increase the productivity of lysine biosynthesis.Following results were received: Activation of TCA-cycle enzymes is compulsory for intensive lysine biosynthesis.The most essential of several parallel electron transport pathways in the ETC of Br. flavum is the NADH dependent, cyanid resistant, hydroxamate sensitive oxydation pathway.Calculations have shown, that the most economical variant is the synthesis of oxalacetate (precursor of lysine) by PEP carboxylation. Therefore strains with elevated PEP-carboxylase activity synthesize lysine in a more economical way.
    Additional Material: 1 Ill.
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  • 38
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 391-392 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: No Abstrct.
    Type of Medium: Electronic Resource
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  • 39
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 131-137 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The propagation of the virulent phage M 1 of the obligate methylotrophic bacteria strain GB 4 is inhibited by n-alkanes. The addition of hydrocarbons (7.5-22.5%) to a suspension of free phages or to a phage-host-mixture prevents the propagation of the phages, but does not influence the growth rate of the host bacteria. In a laboratory fermentor a simulated strong infection (multiplicity = 0.1) of the strain GB 4 with its phage M 1 could be suppressed by the application of 20% of a technical hydrocarbon mixture (Parex I).The inhibitory effect of the hydrocarbons can be traced back to inspecific hydrocarbon-protein-interactions at the surface of the phage and the host cells and therewith to an influencing of the adsorption.
    Additional Material: 3 Ill.
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  • 40
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 139-143 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The influence of microorganisms growing on the walls of laboratory fermenters was investigated and a model to describe of microbial lysis and the formation of growth inhibitory products in a continuous fermentation process was developed.The predictions were compared with results from an earlier model for growth of microorganisms on surfaces.
    Additional Material: 1 Ill.
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  • 41
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 296-299 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: An automatic eightfold-pipetter has been developed with the same basic unit as the diluter of the Autoselect-system. The pipetter is fitted with eight pipettes on a bridge over the basic unit. By means of the pipettes a volume of 0.05 ml from eight tubes is exhauseted and delivered in the holes of a test plate. Both the test plate and a cassette with 64 tubes are located on a moving carriage. the test plate on the first floor and the cassette on the ground floor. If the pipettes transfer the samples from the tubes to the holes the distance between the pipettes must be changed by a special device from 20 to 30 mm, because the distance between the holes on the test plate differs from that of the tubes.For the transfer of 64 samples 2 minutes only are needed.
    Additional Material: 1 Ill.
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  • 42
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 304-307 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 43
    Electronic Resource
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981) 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 44
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 326-326 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
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  • 45
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 338-338 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
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  • 46
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 339-350 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Microbial cells were gel-entrapped with photo-crosslinkable resin prepolymers or urethane prepolymers, respectively. The resulting gels have different tailor-made hydrophobic or hydrophilic character. They were used for successful bioconversion of hydrophobic steroids and terpenoids in watersaturated mixtures of organic solvents. The experiments show the influence of the hydrophobicity of the gels and the polarity of the solvent mixtures, respectively. Use of hydrophobic gels and less polar solvents is preferable for bioconversion of hydrophobic compounds. The selective formation of a desired product among diverse products from a single substrate by appropriate use of hydrophobic or hydrophilic gels is possible. In each case, tests should be made to select the appropriate gel and solvent mixture. Bioconversions tested are: dehydroepiandrosterone to 4-androstene-3,17-dione; cholesterol to cholestenone; β-sitosterol to β-sitostenone; stigmasterol to stigmastenone; pregnenolone to progesterone; testosterone to Δ1-dehydrotestosterone or 4-androstene-3,17-dione, respectively; all with immobilized cells of Nocardia rhodocrous; and stereoselective hydrolysis of dl-menthyl-succinate to yield l-menthol with immobilized cells of Rhodotorula minuta var. texensis.
    Additional Material: 10 Ill.
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  • 47
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 300-303 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: An eightfold punch belonging to the Aùtoselect-system is described. It is provided for the preparation of bioassay plates. From the agar of large quadratic test plates moving automatically on a carriage of the machine, 64 holes are made by eight punches. The punches arranged in a row over the test plate are lowered, if the carriage stops, and so they cut out and exhaust agar discs in a pattern of 8 × 8.
    Additional Material: 1 Ill.
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  • 48
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: No Abstarct.
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  • 49
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 311-325 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Starting with the definition of the process term kLa, steady state and nonsteady state measuring methods are described for its determination. Then the sorption characteristics for mixing vessels and for bubble columns are presented with respect to the coalescence behaviour of the system treated. They permit the scale-up of these devices and the optimization of their process parameters for a required oxygen uptake. In addition to the sorption characteristics for the given system the knowledge of the flooding point and the power characteristics is necessary for the lay-out of mixing vessels, whereas in the case of bubble columns the gas hold-up characteristic needs to be known.
    Additional Material: 10 Ill.
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  • 50
    Electronic Resource
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981) 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
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  • 51
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 3-8 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Auf der Basis der Flotationstheorie der festen Partikel wurde in der Submerskultur der Mechanismus des direkten Sauerstoffübergangs in die Zelle unter den Bedingungen gegenseitiger Beeinflussung des Mikroorganismus mit der gasförmigen und der flüssigen Phase quantifiziert.
    Additional Material: 3 Ill.
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  • 52
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 17-29 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Aus Fermentationen mit Bacillus subtilis, die zum Zwecke der Synthese extrazellulä rer Enzyme angesetzt wurden, konnten verschiedentlich Bakteriophagen isoliert werden. Die auf Grund der Wirtsbereiche differierenden Einzelplaqueisolate wurden elektronenmikroskopisch untersucht. Die Partikel waren sehr verschieden in der Größe und in der morphologischen Struktur. Sie gehörten damit verschiedenen Gruppen von Bacillus-Phagen an, die durch die Standardphagen SPO1, Ø29 und PBS1 reprä sentiert werden. Außerdem wurde ein Phage mit einem oktaedrischen Kopf gefunden. Aus einem enzymbildenden Bacillus-Stamm konnten nach Infektion mit dem PBS1-ä hnlichen Phagen PZ-F Ghosts mit oktaedrischen Köpfen sowie nach Induktion mit Mitomycin C komplette und defektive Phagen freigesetzt werden.
    Additional Material: 16 Ill.
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  • 53
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 9-15 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The capability of the yeast Lodderomyces elongisporus to utilize solved paraffins in fermentation brothes could be demonstrated. The growth rate of this microorganism in the case of utilization of solved paraffins is higher as the most known dates.The saturated concentrations of solved hydrocarbons in the fermentation brothes are higher as in real solvent systems.The part of the solved hydrocarbon is a function of the power input, the diameter of oil drops, the fermentation conditions and the length of the paraffin chain.The organism growth rate depends on the solved paraffin concentration in the fermentation broth. This fact is one of the reasons for the variability of the consumption coefficients by utilization of paraffins with different chain lenghts.The results confirm the assumption that the transport of the paraffins from the oil drops to the cells takes place over water soluble phase.
    Additional Material: 5 Ill.
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  • 54
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 31-40 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Die Xylanaseproduktion durch Streptomyces xylophagus nov. sp. wurde im Schü ttelkolben und in einem 14-Liter-Laborfermentor in diskontinuierlicher und in kontinuierlicher Kultur untersucht. Die maximale Enzymausbeute wurde auf 1%igem handelsü blichen Xylanmedium bei 30°C durch 7,5%ige ü berimpfung einer 5 Tage alten Xylankultur erreicht, wobei dem Medium im Schü ttelkolben 0,8% und dem Submersfermentor 0,3% Bactopepton zugestzt wurden. Die maximale Xylanaseproduktion wurde bei pH 7,4 erreicht. Eine Hitzbehandlung bis zu 200°C wirkte sich nicht hemmend auf die Xylanaseproduktion aus.Die Gleichgewichtsparameter fü r die Zellmasse, lösliches Protein und die Xylanaseaktivitä t wurden in Abhä ngigkeit der Verdü nnungsraten von 0,02 bis 0,04 h+1 bestimmt, wobei Xylan (wood gum xylan) als Kohlenstoffquelle diente. Die maximale Enzymaktivitä t und Produktivitä t von 7,2 X.U. (1 xylanase unit, X.U. ≙ 1 mg reduzierter Zucker, der aus 1 ml Enzym in 15 Minuten bei 50°C gebildet wird) und 0,194 X.U./h wurden bei einer Verdü nnungsrate von 0,027 h+1 beobachtet.Die maximale Zellkonzentration und Produktivitä t von 7,2 g/l und 0,245 g/lh wurden bei einer Verdü nnungsrate von 0,34 h+1 beobachtet.
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  • 55
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 41-47 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Die bei der Herstellung von OYOKPO, einem in der Bendel-Region von Nigeria traditionell auf Hirse-Basis gewonnenem Bier, wirkenden Mikroorganismen wurden untersucht.Die Ergebnisse zeigen zwei Phasen der Einwirkung unterschiedlicher Mikroorganismen.Fü r die saccharolytischen Aktivitä ten beim Mä lzprozeβ sind die aus den gelagerten Hirsekörnern stammenden Mikroorganismen (im Zusammenwirken mit der pflanzlichen Amylase des Hirsemalzes) verantwortlich. Sie werden wahrscheinlich beim Erhitzungsprozeß abgetötet.Die im fermentierten Produkt gefundenen Mikroorganismen stammen aus der fü r die Fermentation eingesetzten Starterkultur; sie vergä ren die niederen Zucker zu Alkohol.Schimmelpilze treten nach der Fermentation nicht mehr auf; Hefen sind wä hrend des Mä lzprozesses nicht zu finden mit Ausnahme von Saccharomyces cervisiae, sie erscheinen jedoch wä hrend der Fermentation. Veschiedene Bakterienarten sind in allen Stadien anzutreffen, so beim Mä lzen, Maischen und bei der Reifung. (Acetobacter wurde bis zu Beginn der Reifung nicht nachgewiesen.) Der pH-Wert sinkt von Beginn der Fermentation (5,2) bis zum Ende auf 3,8. Der am Ende erhaltene Sä urewert entspricht 0,43% (als Essigsä ure titriert).
    Additional Material: 2 Tab.
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  • 56
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 49-56 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Auf der Grundlage von hydrodynamischen und reaktionstechnischen Voraussetzungen wird ein dreiphasiges Stoffsystem mit mikrobieller Reaktion auf quasi-homogene Modelle zurü ckgefü hrt. Mit Hilfe der Michaelis-Menten-Kinetik werden Geschwindigkeitsgleichungen fü r die auto katalytische Reaktion des wachstumsverbundenen Substratabbaues hergeleitet, die sich bis auf die Monod-Kinetik zurü hren lassen. Es wird bewiesen, daß die Geschwindigkeitsgleichungen der mikrobiellen Katalyse denen der heterogenen Gaskatalyse analog sind.
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  • 57
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 57-65 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Growth of Methanosarcina barkeri on methanol as energy source was found to be dependent on cobalt and molybdenum. In the presence of 10-6 M Co and 5 × 10-7M Mo optimal growth occurred. Furthermore it could be demonstrated that nickel and selenium each in a concentration of 10-7 M stimulated the growth of this methanogenic bacterium while the following elements tested in the range of 10-7 M to 10-3 had no influence: B, Cr, Cu, Mn, Pb. The requirement of Co and Ni for optimal growth are in accordance with the results that the cells contain the Co containing corrinoid Factor III (0.1 - 0.2 mg 5-hydroxylbenzimidazolylcyanocobamide per g wet cells) and Factor F430, a nickel component. Studies on the vitamin dependency of M. barkeri showed that this strain needs only the vitamin riboflavin for the growth in a defined medium. Under these conditions a cell density of 2.6 g dry cells/l could be obtained in a fed batch culture.
    Additional Material: 4 Ill.
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  • 58
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 67-72 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
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  • 59
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 73-102 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: A review is given of most of the literature concerning the immobilization of whole microbial cells and their testing for application in product synthesis. The review includes a discussion of adventages and disadventages of immobilized cells, methods of immobilization, pretreatments, aftertreatments, operation, recent developments, and other problems together with a table of the immobilized microbes and the tested reactions of product synthesis, with 350 references.
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  • 60
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 103-103 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
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  • 61
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981) 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
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  • 62
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 107-113 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Rheological measurements can give interesting informations for the characterization of fermentation broth, especially concerning the depending of the oxygen transfer rate. Rheological measurements can report decisions for choosing the best reactor type or other process steps e.g. purification and separation.An advantageous method was used by the combination of a dynamic process-viscosimeter with the fermenter and the continuous measurement of medium density by X-ray absorption method.
    Additional Material: 7 Ill.
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  • 63
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    Acta Biotechnologica 1 (1981), S. 115-126 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The problem of the rate-limiting step of heterogeneous catalytic reactions is explained. For microbiological catalysies in a highdispersial system the partial steps of substance transfer from macroscpace up to the biochemical reaction in the cell (microspace) are generally described and formulated. By means of statistical modells based on the theory of the isotope turbulence the numeric interpretation for the investigation of rate-limiting step at the fermentation and ripening of beer in bioreactors with enforced turbulence takes place. The rate-limiting step is the biochemical reaction of the extract degradation, that means kR·tH ≪ 1.
    Additional Material: 1 Ill.
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  • 64
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981), S. 127-130 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: On the base of measuring the respiration rate (HARRISON) a biological measuring method for determination of methanol concentration in stationary range was worked out. The method allows the determination of methanol concentrations up to 0.3 mg l-1 and is applicable for such cases, when microorganisms consume this substrate quickly (within a few minutes). If the methanol concentration in stationary range is known, it is possible to calculate the kinetic constants of the system.
    Additional Material: 2 Ill.
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  • 65
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    Acta Biotechnologica 1 (1981), S. 145-151 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The influence of extracellular concentrations of hydrogen ion and C-substrates on the specific growth rate of different microorganisms is investigated.A general relationship in the form \documentclass{article}\pagestyle{empty}\begin{document}$$ \mu {\rm } = {\rm }\mu _{\max } {\rm } - {\rm }K_2 \left( {c_i } \right)^{K_1 }$$ \end{document} can be used to describe the inhibition effect of HPlus;- or substrate concentration (ci) on the growth rate. Different examples are demonstrated and the adequate specific constants K1 and K2 calculated.
    Additional Material: 3 Ill.
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  • 66
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    Acta Biotechnologica 1 (1981), S. 153-159 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The improved method for preparing Oyokpo a Nigerian fermented beverage from millet, and the preparation of single cell proteins from the spent grain is described. Improvement of the brew was made by controlled malting, mashing and brewing with a pure culture of Saccharomyces cerevisiae. It had a reducing sugar content of 19.73 g/100 ml before fermentation and after fermentation 5.56% alcohol, 0.58 g/100 ml titratable acidity as acetic acid, a final pH of 4.2 and consisted of a yellowish clear liquid, slightly sour. The native brew had a reducing sugar content of 7.37 g/100 ml before fermentation and after fermentation, 2.40% alcohol, 0.43 g/100 ml titratable acidity, a final pH of 3.8 and consisted of a creamy yellowish liquid with a very sour taste. Fermented spent grain gave a higher protein yield compared to unfermented or ground millet. The lipids, proteins and crude fibre were 4.94%, 11.20% and 4.33% respectively for ground millet, 12,79%, 23.77% and 19.46% respectively for unfermented spent grain and 19.61%, 47.28% and 32.09% respectively for fermented spent grain. The high protein and fibre content of the fermented spent grain points to its potential as a feed supplement for ruminants.
    Additional Material: 1 Ill.
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  • 67
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    Acta Biotechnologica 1 (1981), S. 161-165 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract in Russian.
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  • 68
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The methodical principle of an automated selection system for antibiotic producers, the Autoselectsystem, consisting of six machines and a computer is explained. In order to work with this machines the following material is needed: Cassettes with 64 microculture cups for cultivation of colonies on agar, cassettes with glass-tubes for dilution of samples, and test-plates with 64 holes for performing the agar diffusion test. The cups, the tubes and holes are arranged in a pattern of 8×8. In a serie of papers the machines will be described.
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  • 69
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    Acta Biotechnologica 1 (1981), S. 175-179 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: An agardeliverer, one of the machines of the Autoselect-system is described. This machine allows to pour melted agar automatically into a row of 8 microculture cups of a cassette with 64 cups. By changing the agarcontainer provided for one medium against another container with 8 chambers the machine offers the possibility to deliver 1 to 8 media simultaneously. In this respect the machine gets more and more interest not only for the selection of antibiotic producers, but also for taxonomic, genetic and other studies. Sterile conditions are ensured by sterilizing the head of the machine before starting the work.
    Additional Material: 2 Ill.
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  • 70
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: An inoculator enabling the isolation of colonies from petridishes onto agar-filled microcultur cups, arranged in a pattern of 8 × 8 in cassettes, is described. The transfer of the colonies takes place by turning of an inoculation cross with 4 loops. While the cross stops and lowers, one loop is sterilized, another, which has been sterilized shortly before, is being cooled in sterile water, the next one is taking off some material from a colony and the last is spreading the material on the agar of a cup. The capacity of the machine accounts about 600 colonies per hour.
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  • 71
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    Acta Biotechnologica 1 (1981), S. 187-189 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
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  • 72
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 1 (1981) 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
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  • 73
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    Acta Biotechnologica 1 (1981), S. 197-199 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: It was found that the cellular Na+-concentration (CcellNa+) of Lodderomyces elongisporus D is depended on the extracellular K+-concentration (CexK+).The relationship can be described by an equation in the form \documentclass{article}\pagestyle{empty}\begin{document}$$C_{{\rm cell}}^{Na + } {\rm } = {\rm const}.{\rm } - {\rm const}.{\rm } \cdot {\rm }\ln {\rm }C_{{\rm ex}}^{K + } .$$\end{document}The function of the natrium ion seem to be to support the utilisation rate of potassium ion at lower extracellular K+-concentration.
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  • 74
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    Acta Biotechnologica 1 (1981), S. 268-268 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: No Abstarct.
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  • 75
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    Acta Biotechnologica 1 (1981), S. 269-278 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Fundamentals of bioreactor design are the following functions: macro- and micro-mixing, mass transfer, heat exchange, bioreactor control and its scale-up. Mixing, mass transfer, heat exchange involve the determination of elementary zones of reactor, the mass transfer and the heat exchange between them and also between individual phases (liquid, gaseous, solid), including a possibility of direct gas-cell oxygen uptake. The overall description of a bioreactor is obtained by combining models of reactor hydrodynamics, mass transfer and heat exchange with a appropriate cell or population model. On the basis of hierarchical description new biological scale-up procedures (via modeling and simulation) may evolve.
    Additional Material: 3 Ill.
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  • 76
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    Acta Biotechnologica 1 (1981), S. 285-290 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Aldehyde oxidase from pig liver was adsorptively bound to DEAE-cellulose. The data of immobilization and the properties of the immobilized enzyme are reported. Its maximum half-life is 36 days. The pH-optimum is displaced toward lower pH-values and independent from the substrates proved. Temperature optimum and substrate specifity, however, don't change during immobilization. Contrary to the soluble enzyme the aldehyde oxidase adsorbed to DEAE-cellulose displays a two-phase ARRHENIUS plot.
    Additional Material: 2 Ill.
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  • 77
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: As a part of the Autoselect-system an eightfold diluter is described. Cassettes with 64 tubes are placed on the carriage of the machine and moved automatically in eight steps. One of the cassettes is loaded with separated samples in 64 tubes and the other one with 64 empty tubes. When the carriage stops, a defined volume of samples is exhausted by eight pipettes, mounted on a bridge spanning over the ground unit from left to right, and after beeing moved to the second cassette the pipettes deliver the samples into a row of empty tubes. At the same time by eight syringes mounted on both sides of the machine a defined volume of buffer is delivered through tubes and canules. By this way all samples can be diluted in two minutes.
    Additional Material: 1 Ill.
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  • 78
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The morphology of filamentous microorganisms does essentially affect the production of metabolites. Agitating conditions may affect the morphology and for this reason the production of metabolites too.The following parameters it was found to have an influence: Reynolds mixing numberimpeller blade tips velocitymean shear stress close to the impellerimpeller power consumption per unit volumecavitation pressure dropIt were presumed three mechanisms for the mechanical effect on the microorganisms: 1the direct impact of the impeller blades on the microorganisms-collision2the shear stress in the liquid phase3a sharp pressure decrease behind the impeller blades-cavitationMathematical relationships are developed for the different mechanisms.Using Aspergillus niger it is shown what morphological and physiological states of this microorganism are caused by mechanical straining and the conditions for the maximal production of citric acid are studied.Requirements for scale-up are discussed.
    Additional Material: 8 Ill.
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  • 79
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    Acta Biotechnologica 1 (1981), S. 351-364 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: A general view of the possibilities of producing ethanol from sugar, starch and cellulose feedstocks is given.For the 3 variants net energy analysis of ethanol production and evaluation of costs are presented. With the exception of the case using molasses as feedstock the net energy balances are positive.The greatest possible net energy yield can be expected with sugar cane followed by sugar beets, wood and paper waste. Based on feedstock availability, net energy utilization and production costs, the most promising processes for producing ethanol from non-grain feedstocks over the next 20 years will be those processes using fermentable sugars available from nongrain starchy materials, cellulosics and whey.The feedstock prices for cellulosics are low and if the developments in cellulose hydrolysis will lead to improve the ethanol yields from cellulose fermentation to nearer 90 percent of the theoretical value, cellulosic materials can become a good feedstock for ethanol production.
    Additional Material: 6 Ill.
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  • 80
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    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 41-48 
    ISSN: 0275-3723
    Keywords: hemopoiesis ; leukemia ; hemopoietic progenitors ; cell culture ; stimulatory molecules ; isoelectric focusing ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Medium conditioned by leukocytes in the presence of phytohemagglutinin (PHA-LCM) promotes growth of human hemopoietic progenitors (CFU-GEMM, BFU-E, CFU-C) and precursors of leukemic blast cells. PHA-LCM was separated by isoelectric focusing and each fraction tested with nonadherent cells of normal individuals as well as blast cells from two patients with acute myelogenous leukemia. Activity profiles for CFU-GEMM, BFU-E and CFU-C ranged from pH 5.0-6.5. The profile for activity stimulatory for leukemic blast cells was broader and ranged from pH 5.5-7.5. Although some overlap was observed, the main peaks of stimulatory activity for normally differentiating progenitors and precursors of leukemic blast cells were separable with respect to their isoelectric point.
    Additional Material: 3 Ill.
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  • 81
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    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 49-61 
    ISSN: 0275-3723
    Keywords: labeling of cell surface proteins ; two-dimensional gel electrophoresis ; fibronectin ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: This study was based on our previous findings that the mitogenic action of thrombin on cultured fibroblasts can result from interaction of thrombin with the cell surface in the absence of internalization, and that the proteolytic activity of thrombin is required for stimulation of cell division. This prompted us to look for thrombin-mediated cleavages using 2-dimensional gel electrophoresis of labeled cell surface proteins. Surface membrane components were labeled by 3 procedures: (1) proteins were labeled by lactoperoxidase-catalyzed iodination using 125I-; (2) galactose and galactosamine residues of glycoproteins were oxidized with galactose oxidase and reduced with 3H-NaBH4; and (3) glycoproteins were metabolically labeled by incubating cells with 3H-fucose. Labeling with the first 2 procedures was carried out after thrombin treatment; in contrast, cells metabolically labeled with 3H-fucose were subsequently treated with thrombin to look for proteolytic cleavages. Collectively, these studies indicated that only about 5 cell surface proteins were thrombin-sensitive, consistent with the high specificity of this protease. Each of the labeling procedures revealed a thrombin-sensitive cell surface glycoprotein which was identified as fibronectin by immunoprecipitation experiments. In addition, cell surface proteins of about 140K and 55K daltons were thrombin-sensitive. However, cell surface proteins of about 45K daltons and 130K to 1 50K daltons were increased after thrombin treatment. These experiments were conducted on an established line of Chinese hamster lung cells with the eventual goal of studying thrombin-mediated cleavages of cell surface proteins in a large number of cloned populations derived from this line that are either responsive or unresponsive to the mitogenic action of thrombin. This approach should permit identification of proteolytic cleavages that are necessary for thrombin-stimulated cell division.
    Additional Material: 5 Ill.
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  • 82
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    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 119-128 
    ISSN: 0275-3723
    Keywords: yeast growth ; fatty acids ; phospholipids ; lipid fluidity ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The growth response of a double-mutant fatty acid auxotroph of yeast Saccharomyces cerevisiae to exogenous saturated fatty acids of a homologous series from 12:0 to 16:0, each supplied with oleate, linoleate, linolenate, or cis-Δ11- eicosenoate, cannot be explained in terms of the efficiency of incorporation of the fatty acids into phospholipids or alteration of membrane fluidity. There is, however, a negative correlation between growth and levels of 12:0 plus 13:0 in phospholipids, as well as a positive correlation between growth and levels of 14:0, 1 5:0, and 1 6:0. We, therefore, conclude that the predominant factor in these phospholipid fatty acyl chain modifications is maintenance of an optimal concentration of C14:0 through C16:0 in phospholipids of this organism.
    Additional Material: 2 Ill.
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  • 83
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    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 129-138 
    ISSN: 0275-3723
    Keywords: spectrin ; actin ; erythrocyte ; cytochalasin ; DNase I ; actin polymerization ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The spectrin-4.1-actin complex isolated from the cytoskeleton of human erythrocyte [3] was found to be similar to muscle F-actin in several aspects: Both the complex and F-actin nucleate cytochalasin-sensitive actin polymerization; both bind dihydrocytochalasin B with similar binding constants; both can be depolymerized by DNase I with loss of cytochalasin binding activity. From these results, we conclude that the actin in the complex is in an oligomeric form. However, the presence of spectrin and band 4.1 in the complex not only stabilized the actin in the complex as evidenced by its resistance to depolymerization in low-ionic-strength conditions and to DNase I as compared with F-actin, but also altered the characteristics of the binding site(s) for cytochalasins believed to be located at the “barbed” (polymerizing) end of the oligomeric actin.
    Additional Material: 5 Ill.
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  • 84
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    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 63-72 
    ISSN: 0275-3723
    Keywords: defined medium ; renal epithelium ; tumorigenicity ; primary culture ; PGE ; independent variant ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The possibility has been investigated that (1) the supplements required for the growth of the Madin Darby Canine Kidney (MDCK) cell line in serum-free Medium K-l are indeed requirements for the growth of normal kidney cells in vitro, and (2) that alterations in these growth requirements are associated with malignant transformation. Consistent with the hypothesis that MDCK cells resemble normal kidney cells in culture, primary cultures of baby mouse kidney epithelial cells grow in Medium K-l and respond to the 5 components in the-medium. The growth properties of Moloney sarcoma virus (MSV)-transformed MDCK cells in defined media have been examined. Unlike MDCK cells, MSV-transformed MDCK cells form tumors in adult nude mice. Although they still respond to the 5 factors in Medium K-l, the optimal dosage for insulin is lower for the MSV transformants than for MDCK cells. The MSV transformants also have an additional requirement for growth in Medium K-l - fibronectin. Variants of MDCK cells have been isolated that have lost the PGE1 requirement for growth in defined medium. These variant cells have acquired (1) the ability to form tumors in adult nude mice and (2) an alteration affecting cAMP metabolism, in addition to PGE1 independence.
    Additional Material: 4 Ill.
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  • 85
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    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 73-81 
    ISSN: 0275-3723
    Keywords: erythroid cells ; globin messenger RNA ; heme ; isonicotinic acid hydrazide ; penicillamine ; transcription ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Synthesis of globin mRNA in erythroid spleen cells from anemic mice was measured after in vitro incubation under conditions in which the level of intracellular heme was manipulated. This newly synthesized globin mRNA was isolated by hybridization with globin cDNA covalently bound to cellulose. Isonicotinic acid hydrazide (INH) and penicillamine were used as specific inhibitors of heme synthesis. It has been found that a 120-min incubation of spleen erythroid cells with 5 mM INH or 5mM penicillamine reduced [3H] uridine incorporation into globin mRNA by 24% or 36%, respectively. The addition of heme to INH- or penicillamine-treated cells almost completely restored [3H] uridine incorporation into globin mRNA. These results indicate that heme stimulates transcription or processing of globin mRNA.
    Additional Material: 3 Ill.
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  • 86
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 83-110 
    ISSN: 0275-3723
    Keywords: cell growth ; nutrients ; growth factors ; transformation ; cloning ; kinetic analysis ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The principles of enzyme kinetic analysis were applied to quantitate the relationships among serum-derived growth factors, nutrients, and the rate of survival and multiplication of human fibroblasts in culture. The survival or multiplication rate of a population of cells plotted against an increasing concentration of a growth factor or nutrient in the medium exhibited a hyperbolic pattern that is characteristic of a dissociable, saturable interaction between cells and the ligands. Parameters equivalent to the Km and Vmax of enzyme kinetics were assigned to nutrients and growth factors. When all nutrient concentrations were optimized and in steady state, serum factors accelerated the rate of multiplication of a normal cell population. The same set of nutrients that supported a maximal rate of multiplication in the presence of serum factors supported the maintenance of non-proliferating cells in the absence of serum factors. Therefore, under this condition, serum factors are required for cell division and play a purely regulatory iole in multiplication of the cell population. The quantitative requirement for 18 nutrients of 29 that were examined was significantly higher (P 〈 0.001) for cell multiplication in the presence of serum factors than for cell maintenance in the absence of serum factors. This indicated specific nutrients that may be quantitatively important in cell division processes as well as in cell maintenance. The quantitative requirement for Ca2+, Mg2+, K+, Pi, and 2-oxocarboxylic acid for cell multiplication was modified by serum factors and other purified growth factors. The requirement for over 30 other nutrients could not clearly be related to the level of serum factors in the medium. Serum factors also determined the Ca2+, K+, and 2-oxocarboxylic acid requirement for maintenance of non-proliferating cells. Therefore, when either Ca2+, K+, or 2-oxocarboxylic acid concentration was limiting, factors in serum played a role as cell “survival or maintenance” factors in addition to their role in cell division as “growth regulatory” factors. However, with equivalent levels of serum factors in the medium, the requirement for Ca2+, K+, and 2-oxocarboxylic acids was still much higher for multiplication than for maintenance. Kinetic analysis revealed that the concentrations of individual nutrients modify the quantitative requirement for others for cell multiplication in a specific pattern. Thus, specific quantitative relationships among different nutrients in the medium are important in the control of the multiplication rate of the cell population. When all nutrient concentrations were optimal for multiplication of normal cells, the multiplication response of SV40-virus-transformed cells to serum factors was similar to that of normal cells. When serum factors were held constant, transformed cells required significantly less (P 〈 0.001) of 12 of the 26 nutrients examined. Therefore, the transformed cells only have a growth advantage when the external concentration of specific nutrients limits the multiplication rate of normal cells. Taken together, the results suggest that the control of cell multiplication is intimately related to external concentrations of nutrients. Specific growth regulatory factors may stimulate cell proliferation by modification of the response of normal cells to nutrients. Transforming agents may confer a selective growth advantage on cells by a constitutive alteration of their response to extracellular nutrients.
    Additional Material: 14 Ill.
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  • 87
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    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 139-151 
    ISSN: 0275-3723
    Keywords: metastatic variants ; in vitro correlates ; rat ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: We have studied several metastatic variant cell lines derived from a common clonal origin and their transformed and untransformed parental cell lines. A number of in vitro characteristics were examined for each tumor line and these properties were correlated with the ability of the tumor cells to form pulmonary nodules in an experimental metastasis assay.Direct correlations with metastatic behavior in the lung colony assay were found to exist with the amount of cell-bound Concanavalin A and the procoagulant activities of cell lysates. In vitro parameters that did not correlate with the metastatic phenotype were: population doubling times in culture, saturation density achieved in culture, the number of colony-forming cells shed from confluent cultures, rates of cellular attachment to homotypic or heterotypic cell monolayers, plasminogen-activator production and procoagulant activity produced in serum-free conditioned medium.
    Additional Material: 7 Ill.
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  • 88
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    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 169-176 
    ISSN: 0275-3723
    Keywords: erythropoietin ; macrophages ; silica ; erythrocytic colony-forming units ; polycythemic mouse bioassay ; anti-erythropoietin ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: An erythropoietic stimulating factor (ESF) can be shown to be released from preincubated macrophage-containing cell suspensions from mice by the macrophage-specific, cytotoxic agent, silica. A concentrated silica treated spleen cell supernatant containing ESF is shown to cause a dose dependent increase in 59 Fe incorporation into red blood cells using the in vivo polycythemic mouse bioassay. The ESF from the same supernatant can also be neutralized by anti-erythropoietin. A second concentrated supernatant fractionated using wheat germ lectin-Sepharose 6MB and compared to either unfractionated or fractionated step 111 erythropoietin (Ep), tested in vitro using the erythroid colony-forming technique and 12-day fetal liver as target cells, indicates parallelism of all linear dose-response lines. This, together with the in vivo data, strongly suggests that the ESF released from macrophages treated with silica is, in fact, Ep. Substituting Ca2+ ions for fetal calf serum in the preincubation procedure results in the same activity being released compared to the presence of 1% or 20% fetal calf serum.
    Additional Material: 2 Ill.
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  • 89
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 205-211 
    ISSN: 0275-3723
    Keywords: murine teratocarcinoma ; embryonal carcinoma ; SV40 ; infection ; T antigen ; immunoprecipitation ; replication ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The stem cell of the murine teratocarcinoma is refractory to infection with Simian virus 40 and polyoma. Utilizing various procedures, we attempted to alter this block to infection by modifying the infection procedure. Multiple infections with high-titer SV40 and pretreatment of cells with DEAE-dextran or the carcinogen 4-nitroquinoline l-oxide did not induce embryonal carcinoma cells to produce T- antigen. Co-infection with adenovirus 5, which infects the embryonal carcinoma, and SV40 did not induce the expression of SV40 Tantigen. Therefore, these procedures did not overcome the block to virus infection. The assay for the SV40 T antigen was immunofluorescence; however, the immunoprecipitation technique did not detect T antigen in the infected embryonal carcinoma cells. Finally, the viral DNA present in the embryonal carcinoma was examined for its ability to replicate. These studies showed that viral DNA was not replicating as assayed by the viral DNA's sensitivity to UV irradiation when replicating in the presence of 5-bromodeoxyundine.
    Additional Material: 2 Ill.
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  • 90
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    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 219-234 
    ISSN: 0275-3723
    Keywords: collagen ; SLS ; phospholipid ; surfactant ; fibrillogenesis ; dipalmitoyl phosphatidyl choline ; electrostatic interactions ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The effect of dipalmitoyl phosphatidyl choline (DPPC), the major phospholipid component of pulmonary surfactant, on the precipitation of collagen in the form of native fibrils and segment-long-spacing (SLS) aggregates was studied in vitro. The effects of DPPC on both phases of collagen fibrillogenesis were analyzed spectrophotometrically, and alterations in the morphology of precipitated fibrils and SLS aggregates were ascertained by transmission electron microscopy (TEM). Low concentrations of DPPC inhibited the growth phase of fibrillogenesis, while higher concentrations were required to inhibit nucleation. Both the meshwork density and mean width of precipitated fibrils were altered by DPPC, as was the size of SLS aggregates. Segment-long-spacing aggregates prepared from pepsin-treated collagen were inhibited to a greater degree than SLS aggregates prepared from untreated collagen, indicating that the pepsin-susceptible residues of the telopeptide extensions of tropocollagen molecules stabilize SLS aggregates against the effects of DPPC. Based on these results and the inhibition of the growth phase at lower concentrations than those which inhibited the nucleation phase of fibrillogenesis, it was concluded that the primary mechanism of DPPC inhibition is electrostatic interference between the positively charged phospholipid molecules and the net positive charge of collagen. It is proposed that pathological conditions involving the pulmonary epithelium may allow interaction between surfactant and collagen, which could further weaken the interstitial connective tissue.
    Additional Material: 9 Ill.
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  • 91
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    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 315-315 
    ISSN: 0275-3723
    Keywords: Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Type of Medium: Electronic Resource
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  • 92
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981) 
    ISSN: 0275-3723
    Keywords: Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Type of Medium: Electronic Resource
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  • 93
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 347-358 
    ISSN: 0275-3723
    Keywords: egg receptor for sperm ; cell surface glycoconjugate ; sea urchin fertilization ; sperm-egg binding ; bindin-receptor interaction ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: We have attempted to identify a surface component of echinoderm eggs that is involved in the species-specific binding of sperm. Cell surface membranes from eggs of the sea urchins Strongylocentrotus purpuratus or Arbacia punctulata were radioiodinated, detergent-treated, and subjected to density-gradient centrifugation. In the presence of bindin, the complementary binding protein isolated from sperm, one component of the membranes sedimented to a different density. This membrane component bound-species specifically to sperm that had undergone the acrosome reaction. This binding led to an inhibition of the ability of treated sperm to fertilize eggs. Exhaustive proteolytic digestion of this receptor fraction yields a high molecular weight glycopeptide that can also bind to bindin. It therefore appears that this egg surface membrane fraction contains a functionally intact, species-specific receptor for sperm.
    Additional Material: 7 Ill.
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  • 94
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    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 369-385 
    ISSN: 0275-3723
    Keywords: membrane phosphoproteins ; cAMP in development ; Dictyostelium discoideum ; phospho proteins ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The phosphoproteins of Dictyostelium discoideum were compared at different stages of development by polyacrylamide gel electrophoresis. Certain phosphoproteins of vegetative amoebae were conserved while others appeared and disappeared during development. Four major phosphoproteins with apparent subunit molecular weights of 50,000, 47,000, 38,000, and 34,000 disappeared precociously in response to exogenous cAMP. Two membranal phosphoproteins, with apparent subunit molecular weights of 80,000 and 81,000, appeared precociously in response to added cAMP. One of these phosphoproteins, molecular weight of 80,000, has been identified tentatively as the “contact site A” glycoprotein. Another membranal protein, with apparent subunit molecular weight of 42,000, unaffected in its appearance by cAMP, has been identified tentatively as phosphoactin.
    Additional Material: 7 Ill.
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  • 95
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    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 387-394 
    ISSN: 0275-3723
    Keywords: egg receptor for sperm ; cell surface glycoconjugate ; sea urchin fertilization ; sperm-egg binding ; bindin-receptor interaction ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Sea urchin sperm-egg adhesion is mediated by bindin, a sperm surface protein that has lectin-like activity. Bindin agglutinates eggs, and this interaction has been shown to be inhibited by glycopeptides released from the egg surface by protease treatment. In this study, we report the purification and properties of such an egg surface glycoconjugate that may be involved in sperm adhesion. The glycoconjugate was partially purified by gel filtration and affinity chromatography on bindin particles. Upon gel filtration on Sepharose CL 4-B, the glycoconjugate elutes near the void volume, suggesting that it has a molecular weight in excess of one million. In addition, we have found that the egg surface glycoconjugate agglutinates bindin particles, indicating that it is multivalent. Carbohydrate analysis indicates that the glycoconjugate is composed primarily of fucosc, xylose, galactose, and glucose. This purified egg surface component is the most potent inhibitor of bindin-mediated egg agglutination yet described.
    Additional Material: 4 Ill.
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  • 96
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    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 327-333 
    ISSN: 0275-3723
    Keywords: sea urchin ; cell adhesions ; cell-cell adhesions ; protease effects ; glycopeptidcs ; cell surface protein ; azide ; cytochalasin B ; protease release ; endogenous inhibitor ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: To understand the nature of the cell adhesions that must be modified during sea urchin embryo primary mesenchyme formation, we are studying the adhesive components of the hatched blastula stage embryo of Strongylocentrotus purpuratus. Pronase treatment conditions have been defined that leave the cells intact and able to recover from the effects of the protease upon its removal. Under these conditions, adhesion of the cells to tissue culture plates is totally eliminated, but cell-cell adhesion formation is only partially inhibited. Analysis of iodinated cell surface proteins indicates that most are affected by thepronase. Further studies of pronase effects found that sodium azide-treated cells are slightly adhesive and that pronase treatment of azidc-treated cells totally eliminates cell-cell adhesions.
    Additional Material: 3 Ill.
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  • 97
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    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 16 (1981), S. 345-358 
    ISSN: 0275-3723
    Keywords: fibronectin ; evolution ; proteolytic fragment ; domain structure ; receptor ; glycoprotein ; cellular adhesion ; adhesion placque ; cell surface protein ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Fibronectin is a large, adhesive glycoprotein which is found in a number of locations, most notably on cell surfaces, in extracellular matrixes, and in blood. Fibronectin has been detected in all vertebrates tested and in many invertebrates. Its presence in sponges is significant because this suggests that fibronectin may have appeared very early in evolution, possibly with the most primitive multicellular organisms. Cellular and plasma fibronectins have many striking similarities. However, the locations of the polypcptide chain differences between these two proteins indicate that plasma fibronectin cannot be derived from cellular fibronectin by means of simple post-translational proteolysis. Instead, these different types of fibronectin may be products of different genes or of differentially spliced messenger RNA molecules. Amniotic fluid fibronectin is possibly a third form of the protein. Cellular and plasma fibronectins are composed of at least six protcaseresistant domains which contain specific binding sites for actin, gelatin, heparin, Staphylococcus aureus, transglutarninase, fibrin, DNA, and a cell surface receptor. The relative locations of these domains have been mapped in the primary structure of fibronectin. The cell surface receptor for fibronectin has not been positively identified, but may be a glycoprotein, a glycolipid, or a complex of the two. Although cell-substratum adhesion is mediated by fibronectin, the locations of the areas of closest approach of the cell to the substratum (the adhesion plaques) and fibronectin are not coincident under conditions of active cell growth. Under conditions of cell growth arrest in low scrum concentrations, some fibronectin may become localized at the adhesion plaques. Models describing the domain structure of fibronectin and the molecular organization of the adhesion plaque area are presented.
    Additional Material: 3 Ill.
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  • 98
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    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 16 (1981), S. 359-370 
    ISSN: 0275-3723
    Keywords: anti-hapten + self CTL ; T helper ; CTL clones ; (non)-responder strain ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Requirements for stimulation of cytotoxic T cells (CTL) and for their lytic recognition have been compared in T cell lines repeatedly stimulated with trinitrobenzene sulfonate-treated syngeneic murine spleen cells. Differences were observed between the requirements for cells to stimulate or to be lysed by the CTL, which included: (a) the expression of major histocompatibility complex (MHC = H-2) encoded allelic products, and (b) the hapten density. Propagation of the CTL within the line required I-A intra-H-2 homology between hapten-treated stimulating cells and the line cells, whereas the lytic interaction required H-2K region homology between hapten-treated target cells and CTL. The hapten density requirement was analyzed for a responder (H-2k) and a non-responder (H-2b) strain to low hapten density modified syngeneic cells. This property was found to be a characteristic of the lytic phase rather than of the stimulation of CTL. CTL clones could be derived by growing the line cells under conditions of limiting dilution in the presence of T cell growth factors. Such CTL clones were unable to be stimulated by their target antigens and were dependent on T cell growth factors for their propagation. These results are discussed in terms of the dependence of the development and growth of CTL on T helper cells.
    Additional Material: 6 Tab.
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  • 99
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 17 (1981), S. 153-161 
    ISSN: 0275-3723
    Keywords: difference between cellular and plasma forms ; fibronectin ; monoclonal antibodies ; structure and function ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The reactivity of six monoclonal antibodies with fragments of fibronectin produced with trypsin, chymotrypsin, and Staphylococcus aureus V8 protease is described. All these antibodies reacted with fragments derived from the C-terminal one-third of fibronectin. This region probably contains sites for the binding of fibronectin to cells, and to heparin and may also contain active sites for the reattachment, spreading, and alignment of transformed cells. Analysis of the reactivities of different sets of proteolytic fragments with the antibodies and with other ligands (eg. heparin) allows one to determine overlaps between the fragments and to locate the positions of the different binding sites for antibodies and ligands. One of the antibodies has allowed us to identify a site of structural difference between cellular and plasma fibronectins from hamsters. The site recognized by this antibody is located near to, but not at, the C-terminal end and docs not involve carbohydrate groups. Because of its internal location in fibronectin, this difference suggests that there are probably different genes for cellular and plasma fibronectin. These monoclonal antibodies should be useful for further probing the functions present in the C-terminal regions of fibronectin and for determining their locations.
    Additional Material: 4 Ill.
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  • 100
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Journal of Supramolecular Structure and Cellular Biochemistry 15 (1981), S. 1-13 
    ISSN: 0275-3723
    Keywords: insulin receptors ; photoaffinity labeling ; electrophoresis ; Chemistry ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Photoaffinity labeling techniques were used to identify insulin-binding components of the plasma membrane in insulin-responsive, monolayer-cultured hepatoma cells. The activated, photosensitive reagent, an n-hydroxysuccinimide ester of 4-azidobenzoic acid, was coupled with highly purifed insulin, and the hormone derivative was subsequently iodinated, bound to cell surface receptors of intact H4 cells, and photoactivatcd. After dissolution of the cells, labeled proteins were analyzed by SDS/polyacrylamide gel electrophoresis under reducing conditions. The main labeled band exhibited an apparent molecular weight of 130,000. Two minor components of apparent mol wt 95,000 and 40,000 were also identified. Specific labeling of all 3 bands was inhibited by simultaneous incubation of the cells with native insulin, but not by the heterologous hormone, glucagon, prior to photoactivation. Binding of azidobenzoyl-insulin to H4 cells was time-dependent, as was the correlated labeling of receptor components. Band-labeling by the photosensitive insulin derivative was totally light-dependent; spontaneous covalent linking of insulin and receptor was not observed. The labeled receptor-related proteins were not degraded by the cells under our experimental conditions.
    Additional Material: 6 Ill.
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