Kinetics and modeling of the stereoselective reduction of acetoacetic acid esters by continuously growing cultures of Saccharomyces cerevisiae

Author:

Rohner Markus,Locher Georg,Sonnleitner Bernhard,Fiechter Armin

Publisher

Elsevier BV

Subject

Applied Microbiology and Biotechnology,General Medicine,Biotechnology,Bioengineering

Reference24 articles.

1. Stereoselective reduction of non-cyclic carbonyl compounds by some eumycetes;Aragozzini;Appl. Microbiol. Biotechnol.,1986

2. Asymmetric reduction of carbonyl compounds by yeast. IV. Preparation of optically active β-hydroxy sulfides, sulfoxides and sulfones;Crumbie;Aust. J. Chem.,1978

3. Asymmetric reduction of carbonyl compounds by yeast. II: Preparation of optically active α- and β-hydroxycarboxylic acid derivatives;Deol;Aust. J. Chem.,1976

4. Stereoselectivity of yeast reductions — an improved procedure for the preparation of ethyl (S)-3-hydroxibutanoate and (S)-2-hydroxymethylbutanoate;Ehrler;Chimia,1986

5. The chemostat — an efficient technique for medium optimization;Goldberg;Process Biochem.,1981

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1. Reduction of ethyl 3-oxobutanoate using non-growing baker’s yeast in a continuously operated reactor with cell retention;Enzyme and Microbial Technology;2002-10

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3. Biotransformation for l-ephedrine production;Biotreatment, Downstream Processing and Modelling;1997

4. Functional state modelling approach for bioprocesses: local models for aerobic yeast growth processes;Journal of Process Control;1994-08

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