Literature DB >> 10068792

Biotransformation of nitriles by rhodococci.

A W Bunch1.   

Abstract

Rhodococci have been shown to be capable of a very wide range of biotransformations. Of these, the conversion of nitriles into amides or carboxylic acids has been studied in great detail because of the biotechnological potential of such activities. Initial investigations used relatively simple aliphatic nitriles. These studies were quickly followed by the examination of the regio- and stereoselective properties of the enzymes involved, which has revealed the potential synthetic utility of rhodococcal nitrile biotransforming enzymes. Physiological studies on rhodococci have shown the importance of growth medium design and bioreactor operation for the maximal conversion of nitriles. This in turn has resulted in some truly remarkable biotransformation activities being obtained, which have been successfully exploited for commercial organic syntheses (e.g. acrylamide production from acrylonitrile). The two main types of enzyme involved in nitrile biotransformations by rhodococci are nitrile hydratases (amide synthesis) and nitrilases (carboxylic acid synthesis with no amide intermediate released). It is becoming clear that many rhodococci contain both activities and multiple forms of each enzyme, often induced in a complex way by nitrogen containing molecules. The genes for many nitrile-hydrolysing enzymes have been identified and sequenced. The crystal structure of one nitrile hydratase is now available and has revealed many interesting aspects of the enzyme structure in relationship to its catalytic activity and substrate selectivity.

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Year:  1998        PMID: 10068792     DOI: 10.1023/a:1001760129546

Source DB:  PubMed          Journal:  Antonie Van Leeuwenhoek        ISSN: 0003-6072            Impact factor:   2.271


  7 in total

1.  Nitrilase-catalysed conversion of acrylonitrile by free and immobilized cells of Streptomyces sp.

Authors:  V K Nigam; A K Khandelwal; R K Gothwal; M K Mohan; B Choudhury; A S Vidyarthi; P Ghosh
Journal:  J Biosci       Date:  2009-03       Impact factor: 1.826

2.  Nitrosative cytosine deamination. An exploration of the chemistry emanating from deamination with pyrimidine ring-opening.

Authors:  Sundeep Rayat; Ming Qian; Rainer Glaser
Journal:  Chem Res Toxicol       Date:  2005-08       Impact factor: 3.739

3.  Bacterial diversity in three different Antarctic Cold Desert mineral soils.

Authors:  Jacques J Smith; Lemese Ah Tow; William Stafford; Craig Cary; Donald A Cowan
Journal:  Microb Ecol       Date:  2006-04-05       Impact factor: 4.552

4.  An improved nitrilase-mediated bioprocess for synthesis of nicotinic acid from 3-cyanopyridine with hyperinduced Nocardia globerula NHB-2.

Authors:  Nitya Nand Sharma; Monica Sharma; Tek Chand Bhalla
Journal:  J Ind Microbiol Biotechnol       Date:  2010-11-21       Impact factor: 3.346

5.  Microbial isobutyronitrile utilization under haloalkaline conditions.

Authors:  Dimitry Y Sorokin; Sander van Pelt; Tatjana P Tourova; Gerard Muyzer
Journal:  Appl Environ Microbiol       Date:  2007-07-20       Impact factor: 4.792

6.  Characterisation of the substrate specificity of the nitrile hydrolyzing system of the acidotolerant black yeast Exophiala oligosperma R1.

Authors:  S Rustler; A Chmura; R A Sheldon; A Stolz
Journal:  Stud Mycol       Date:  2008       Impact factor: 16.097

Review 7.  Membrane transport systems and the biodegradation potential and pathogenicity of genus Rhodococcus.

Authors:  Carla C C R de Carvalho; Sofia S Costa; Pedro Fernandes; Isabel Couto; Miguel Viveiros
Journal:  Front Physiol       Date:  2014-04-04       Impact factor: 4.566

  7 in total

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