Literature DB >> 12529882

Use of the two-liquid phase concept to exploit kinetically controlled multistep biocatalysis.

Bruno Bühler1, Irene Bollhalder, Bernhard Hauer, Bernard Witholt, Andreas Schmid.   

Abstract

The two-liquid phase concept was used to develop a whole cell biocatalytic system for the efficient multistep oxidation of pseudocumene to 3,4-dimethylbenzaldehyde. Recombinant Escherichia coli cells were employed to express the Pseudomonas putida genes encoding xylene monooxygenase, which catalyzes the multistep oxygenation of one methyl group of toluene and xylenes to corresponding alcohols, aldehydes, and acids. A fed-batch based two-liquid phase bioconversion was established with bis(2-ethylhexyl)- phthalate as organic carrier solvent and a phase ratio of 0.5; the product formation pattern, the impact of the nutrient feeding strategy, and the partitioning behavior of the reactants were studied. On the basis of the favorable conditions provided by the two-liquid phase system, engineering of the initial pseudocumene concentration allowed exploiting the complex kinetics of the multistep reaction for the exclusive production of 3,4-dimethyl- benzaldehyde. Further oxidation of the product to 3,4-dimethylbenzoic acid could be inhibited by suitable concentrations of pseudocumene or 3,4-dimethylbenzyl alcohol. The optimized biotransformation setup includes a completely defined medium with high iron content and a nutrient feeding strategy that avoids severe glucose limitation as well as high inhibitory glucose levels. Using such a system on a 2-liter scale, we were able to produce, within 14.5 h, 30 g of 3,4-dimethylbenzaldehyde as predominant reactant in the organic phase and reached a maximal productivity of 1.6 g per liter liquid volume per hour. The present study implicates that the two-liquid phase concept is an efficient tool to exploit the kinetics of multistep biotransformations in general. Copyright 2003 Wiley Periodicals. Biotechnol Bioeng 81: 683-694, 2003.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12529882     DOI: 10.1002/bit.10512

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  20 in total

1.  Making variability less variable: matching expression system and host for oxygenase-based biotransformations.

Authors:  Martin Lindmeyer; Daniel Meyer; Daniel Kuhn; Bruno Bühler; Andreas Schmid
Journal:  J Ind Microbiol Biotechnol       Date:  2015-04-16       Impact factor: 3.346

2.  Regioselective aromatic hydroxylation of quinaldine by water using quinaldine 4-oxidase in recombinant Pseudomonas putida.

Authors:  F Ozde Utkür; Sushil Gaykawad; Bruno Bühler; Andreas Schmid
Journal:  J Ind Microbiol Biotechnol       Date:  2010-10-02       Impact factor: 3.346

3.  Whole-cell biocatalysis for 1-naphthol production in liquid-liquid biphasic systems.

Authors:  S V B Janardhan Garikipati; Angela M McIver; Tonya L Peeples
Journal:  Appl Environ Microbiol       Date:  2009-08-21       Impact factor: 4.792

4.  The dynamic influence of cells on the formation of stable emulsions in organic-aqueous biotransformations.

Authors:  Jonathan Collins; Marcel Grund; Christoph Brandenbusch; Gabriele Sadowski; Andreas Schmid; Bruno Bühler
Journal:  J Ind Microbiol Biotechnol       Date:  2015-04-28       Impact factor: 3.346

5.  Integrated organic-aqueous biocatalysis and product recovery for quinaldine hydroxylation catalyzed by living recombinant Pseudomonas putida.

Authors:  F Ozde Ütkür; Tan Thanh Tran; Jonathan Collins; Christoph Brandenbusch; Gabriele Sadowski; Andreas Schmid; Bruno Bühler
Journal:  J Ind Microbiol Biotechnol       Date:  2012-03-02       Impact factor: 3.346

6.  Engineering of Pseudomonas taiwanensis VLB120 for constitutive solvent tolerance and increased specific styrene epoxidation activity.

Authors:  Jan Volmer; Christoph Neumann; Bruno Bühler; Andreas Schmid
Journal:  Appl Environ Microbiol       Date:  2014-08-15       Impact factor: 4.792

7.  Application of AlkBGT and AlkL from Pseudomonas putida GPo1 for Selective Alkyl Ester ω-Oxyfunctionalization in Escherichia coli.

Authors:  Youri M van Nuland; Gerrit Eggink; Ruud A Weusthuis
Journal:  Appl Environ Microbiol       Date:  2016-06-13       Impact factor: 4.792

8.  Outer membrane protein AlkL boosts biocatalytic oxyfunctionalization of hydrophobic substrates in Escherichia coli.

Authors:  Mattijs K Julsing; Manfred Schrewe; Sjef Cornelissen; Inna Hermann; Andreas Schmid; Bruno Bühler
Journal:  Appl Environ Microbiol       Date:  2012-06-08       Impact factor: 4.792

9.  Cell physiology rather than enzyme kinetics can determine the efficiency of cytochrome P450-catalyzed C-H-oxyfunctionalization.

Authors:  Sjef Cornelissen; Shanshan Liu; Amit Tatyasaheb Deshmukh; Andreas Schmid; Bruno Bühler
Journal:  J Ind Microbiol Biotechnol       Date:  2011-05-11       Impact factor: 3.346

10.  Proline availability regulates proline-4-hydroxylase synthesis and substrate uptake in proline-hydroxylating recombinant Escherichia coli.

Authors:  Francesco Falcioni; Lars M Blank; Oliver Frick; Andreas Karau; Bruno Bühler; Andreas Schmid
Journal:  Appl Environ Microbiol       Date:  2013-03-01       Impact factor: 4.792

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.