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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 135 (1983), S. 30-35 
    ISSN: 1432-072X
    Keywords: Rhodophyta ; Cyanidium caldarium ; Biliprotein ; Levulinic acid ; δ-aminolevulinic acid incorporation ; Phycocyanin apoprotein
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Cultures of the unicellular red alga Cyanidium caldarium were transferred from heterotrophic growth conditions to photoautotrophic growth. During photoautotrophic growth, the biliprotein phycocyanin is synthesized de novo. In the presence of 2–5 mM/l levulinic acid which inhibits the biosynthesis of tetrapyrrole chromophores, phycocyanin biosynthesis is suppressed by a factor of 29. Immunoprecipitation yields small amounts of “apoprotein” i.e. phycocyanin which lacks all or part of its chromophore(s). In various experiments the ratio apoprotein/residual holoprotein (phycocyanin) was determined as 2–6 to one. Incubation with [3H]leucine leads to labelled immunoprecitable material: apoprotein (18,300–19,600 Mr) and larger poly-peptides (50,000–52,000 Mr) of unknown nature. The apoprotein was separated from residual phycocyanin by chromatography on DEAE-cellulose and preparative isoelectric focusing (IEF). The significance of the results for further studies on the last steps of phycocyanin biosynthesis is discussed.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The total synthesis of racemic cis-2,3,181, 182, -tetrahydroprotobiliverdin IXα dimethyl ester (19b), which is identical with the dimethyl ester of rac-4, is described (Scheme 2). Under virtually neutral conditions, in solution, this bile pigment isomerized within a few min to racemic Z-phycocyanobilin dimethyl ester (rac-5b). Likewise, acid-catalyzed allyl rearrangement of 3-vinyl-substituted cis- and trans-2,3-dihydrodipyrrin-1(10H)-ones 11c and 13c, respectively, yielded the corresponding ethylidene derivatives. In this case, however, the E-isomer was formed stereo selectively from both substrates. The above results prove that, if protobiliverdin IXα (2) is transformed enzymatically to its 2,3,181, 182-tetrahydro derivative, the latter would isomerize spontaneously to phycocyanobi-lin. The biosynthesis of bacteriochlorophyll a and b from a common precursor bearing a vinyl group at C(8)may be straightforwardly explained in the same way.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 738 (1970), S. 197-201 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Structure of MesobilirhodinStructure 9 is proposed for the bile pigment mesobilirhodin based on its electronic and mass spectra and its chromic acid degradation which yields methylethylmaleinimide (5), haematinic acid imide methyl ester (6) andtrans-methylethylsuccinimide (7).
    Notes: Für den Gallenfarbstoff Mesobilirhodin wird aufgrund der Elektronen- und Massenspektren sowie des Chromsäureabbaus, der zu Methyläthylmaleinimid (5), Hämatinsäureimid-methyl-ester (6) und trans-Methyläthylsuccinimid (7) führt, die Struktur 9 vorgeschlagen.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Bonding between Chromophore and Protein in Biliproteins, I. - Degradation Experiments and Spectral Investigations on BiliproteinsDegradation experiments with nine different biliproteins show that ring A of the chromophore and one of the middle rings (in phycoerythrin identified as ring C) are always covalently linked with the apoprotein. According to spectral investigations, the chromophore of phycoerythrin contains six, and that of phycocyanin nine conjugated double bonds. One additional double bond is formed during splitting of the chromophore with boiling methanol. Partial structure 11 containing the linkage to the apoprotein is proposed for the phycoerythrin chromophore on the basis of kinetics of isomerization to a urobilin.
    Notes: Abbauversuche an neun verschiedenen Biliproteiden zeigen, daß immer jeweils Ring A des Chromophors und einer der mittleren Ringe (bei Phycoerythrinen als Ring C identifiziert) mit dem Protein kovalent verknüpft sind. Nach Spektraluntersuchungen besitzt der Chromophor des Phycoerythrins sechs, der des Phycocyanins neun konjugierte Doppelbindungen. Bei der Abspaltung der Chromophore mit siedendem Methanol kommt jeweils eine Doppelbindung hinzu. Für den Phycoerythrin-Chromophor wird aufgrund der Kinetik der Isomerisierung in ein Urobilin die Teilstruktur 11 vorgeschlagen, die die Bindungsstelle zum Protein berücksichtigt.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Bonding between Chromophore and Protein in Biliproteins, II. - Detection of Cysteine as Binding Amino Acid in B-PhycoerythrinB-Phycoerythrin from Porphyridium cruentum is degraded to bilipeptides by pepsin. The bile pigment is removed by Edman degradation together with N-terminal cysteine from a mixture of small bilipeptides (fraction I). Further pepsin digestion yields a tripeptide (fraction 2) containing the bile pigment, cysteine, valine, and leucine. Edman degradation leads to the red product 1. The thiol group of cysteine was recognized as the binding group at the side chain of Ring A of the bile pigment.
    Notes: B-Phycoerythrin aus Porphyridium cruentum wird mit Pepsin zu Bilipeptiden abgebaut. Aus einem Gemisch kurzkettiger Bilipeplide (Fraktion I) wird der Galienfarbstoff zusammen mil dem N-terminalen Cystein beim Edman-Abbau abgespalten. Der weitere Pepsin-Abbau führt zu einem Tripeptid (Fraktion 2), das den Gallenfarbstoff, Cystein, Valin und Leucin enthält. Beim Edman-Abbau entsteht das rote Produkt 1. Als Bindungstelle an der Seiten- kette von Ring A des Farbstoffs wurde die Thiolgruppe von Cystein ermittelt.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electrophoresis 13 (1992), S. 660-661 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Isoelectric focusing (IEF) runs, e.g. on ultrathin gels, are characterized by an extensive change of gel electric parameters, caused by the rearrangement of carrier ampholyte components from a uniform distribution to a highly ordered pH gradient. A particularly important parameter is the specific resistance ϱ [Ohm*cm] which has been determined in polymerization mixtures (with and without carrier ampholytes) and in 125× 0.15 mm ultrathin gels, pH 3-10 with 5 %T, 3 %C, 5 % Servalyt carrier ampholytes, pH 3-10. The starting specific resistance ϱ of ultrathin IEF gels, calculated from the geometric gel dimensions and electric current values (V, mA), is in agreement with the data determined directly in 30 mL samples of polymerization mixtures by using a conductivity meter. Electric specific conductivity/Volthour (Vh) plots proved to be a valuable tool for the evaluation of gel systems with and without protein samples during IEP runs. These plots are usually S-shaped, indicating that the key part of pH gradient formation takes places in a relatively short time. A “good” ultrahin gel, after a short lag phase, shows a rapid increase in specific resistance due to a rapid pH gradient formation and a slope of about 18 Ohm*cm/Vh. IEF is finished in about 3000 Vh. After prolonged gel storage, and especially in partially dried gels, the electrical parameters approach equilibrium only slowly, as indicated by the relatively shallow slope (8.9 Ohm*cm/Vh). Accordingly, separations need more than 4000 Vh. In gels with salt containing samples, after normal IEF for about 1750 Vh, cracks appear, often followed by sparking at about 2700 Vh, accompanied by a sharp (often intermittent) drop in specific resistance.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electrophoresis 4 (1983), S. 148-152 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: It is demonstrated that photoacoustic spectroscopy is a superior tool in the evaluation of electropherograms. The locla distribution of proteins in ultrathin layers of polyacrylamide gels used for isoelectric focusing is mapped with a resolution equal to or better than a laster densitomer. Even unstained samples of colored proteins can be mapped with excellent sensitivity and resolution due to the fact that the photoacoustic effect is caused only by the absorbed fraction of the incident light; scapttered light therefore doesse not cause a signal. in situ photoacosutic spectra of previously localzed zones allow the identification of the prosthetic groups of these proteins.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A new method is presented for the fast preparative separation of the light-harvesting photosynthetic pigment C-phycocanin into its α and β subunits, which is based on isoelectric focusing in layers of granutaled gels containing 7 M urea. The method has been successful in cases where other separation procedures failed. The recovery of the separated chains of the light -sensitive biliprotein amounts to 70 ± 10 % when the separation is carried out under light exclusion and in an argon atmosphere. A simple and inexpensive setup for work under an atmosphere of protective gas is described.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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