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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 745 (1994), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Biotechnology letters 22 (2000), S. 807-812 
    ISSN: 1573-6776
    Keywords: azo dye ; decolorization ; Escherichia coli
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract A recombinant Escherichia coli strain (E. coli NO3) containing genomic DNA fragments from azo-reducing wild-type Pseudomonas luteola strain decolorized a reactive azo dye (C.I. Reactive Red 22) at approx. 17 mg dye h−1 g cell. The ability to decolorize the azo dye probably did not originate from the plasmid DNA. Acclimation in azo-dye-containing media gave a nearly 10% increase in the decolorization rate of E. coli NO3. Growth with 1.25 g glucose l−1 completely stopped the decolorization activity. When the decolorization metabolites from E. coli NO3 were analyzed by HPLC and MS, the results suggested that decolorization of the azo dye may be due to cleavage of the azo bond.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-6776
    Keywords: bio-conversion ; carbamoylase ; hydantoinase ; hydroxyphenylglycine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract By use of PCR, the genes encoding d-carbamoylase and d-hydantoinase, responsible for the synthesis of d-p-hydroxyphenylglycine (d-HPG), were cloned separately from Agrobacterium radiobacter NRRL B11291 into Escherichia coli. d-HPG production was carried out with a mixed population consisting of various proportions of two recombinants producing individual enzymes. As a result, with a total amount of 192 mg dry cell, the optimal productivity of d-HPG (ca. 4.5 g h−1 l−1) was obtained when the ratio of d-carbamoylase to d-hydantoinase ranged between 1 and 2.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 40 (1994), S. 1580-1593 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: General procedures are outlined for the simulation and propagation of random and systematic errors in thermophysical property experiments. Density second virial coefficients B(T) from sonic velocity and Joule-Thomson (J-T) experiments are examined for error propagation where the connecting thermodynamic identity is a differential equation with missing boundary conditions. A recent controversy is addressed concerning B(T) at subcritical temperatures for pure hydrocarbon gases from direct density measurements vs. new sonic velocity data. Sonic velocity results are more likely correct with adsorption errors causing the problem in the density measurements.Two new model consistency tests are developed for checking assumed temperature models in the reduction of sonic velocity and J-T data to B(T). Excellent values of B(T) are then obtained from either type of data when the original experiments are free of errors. Random errors propagate systematically when the connecting equation is a differential equation. Sonic data must be of high precision (± 10 ppm) to generate B(T) to ±1 cm3/mol due to complications in data reduction arising from the temperature model/random error interaction. Except perhaps for adsorption errors, systematic errors in the sonic velocities are unimportant to B(T). J-T data provide propagation factors near unity with errors in B(T) higher at higher temperature, unlike sonic velocities.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 52 (1996), S. 129-140 
    ISSN: 0006-3592
    Keywords: pathway engineering ; central metabolism ; phosphoenolpyruvate synthase ; phosphoenolpyruvate carboxykinase ; aromatic amino acid ; Escherichia coli ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The rate and yield of producing a metabolite is ultimately limited by the ability to channel metabolic fluxes from central metabolism to the desired biosynthesis pathway. Redirection of central metabolism thus is essential to high-efficiency production of biochemicals. This task begins with pathway analysis, which considers only the stoichiometry of the reaction networks but not the regulatory mechanisms. An approach extended from convex analysis is used to determine the basic reaction modes, which allows the determination of optimal and suboptimal flux distributions, yield, and the dispensable sets of reactions. Genes responsible for reactions in the same dispensable set can be deleted simultaneously. This analysis serves as an initial guideline for pathway engineering. Using this analysis, we successfully constructed an Escherichia coli strain that can channel the metabolic flow from carbohydrate to the aromatic pathway with theoretical yield. This analysis also predicts a novel cycle involving phosphoenolpyruvate (PEP) carboxykinase (Pck) and the glyoxylate shunt, which can substitute the tricarboxylic acid cycle with only slightly less efficiency. However, the full cycle could not be confirmed in vivo, possibly because of the regulatory mechanism not considered in the pathway analysis.In addition to the kinetic regulation, we have obtained evidence suggesting that central metabolites are involved in specific regulons in E. coli. Overexpression of PEP-forming enzymes (phosphoenolpyruvate synthase [Pps] and Pck) stimulates the glucose consumption rate, represses the heat shock response, and negatively regulates the Ntr regulon. These results suggest that some glycolytic intermediates may serve as a signal in the regulation of the phosphotransferase system, heat shock response, and nitrogen regulation. However, the role of central metabolites in these regulations has not been determined conclusively. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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