Advances in Biochemical Engineering/Biotechnology, volume 113, pages 33-77
Microbial Transformation of Nitriles to High-Value Acids or Amides
Jing Chen
1
,
Ren Chao Zheng
1
,
Yu-Guo Zheng
1
,
Yin-Chu Shen
1
Publication type: Book Chapter
Publication date: 2009-10-13
scimago Q3
SJR: 0.346
CiteScore: 5.7
Impact factor: —
ISSN: 07246145, 16168542
PubMed ID:
19475377
Abstract
Biotransformation of nitriles mediated by nitrile-amide converting enzymes has attracted considerable attention and developed tremendously in the recent years in China since it offers a valuable alternative to traditional chemical reaction which requires harsh conditions. As a result, an upsurge of these promising enzymes (including nitrile hydratase, nitrilase and amidase) has been taking place. This review aims at describing these enzymes in detail. A variety of microorganisms harboring nitrile-amide converting activities have been isolated and identified in China, some of which have already applied with moderate success. Currently, a wide range of high-value compounds such as aliphatic, alicyclic, aromatic and heterocyclic amides and their corresponding acids were provided by these nitrile-amide degra-ding organisms. Simultaneously, with the increasing demand of chiral substances, the enantioselectivity of the nitrilase superfamily is widely investigated and exploited in China, especially the bioconversion of optically active α-substituted phenylacetamides, acids and 2,2-dimethylcyclopropanecarboxamide and 2,2-dimethylcyclopropanecarboxylic acid by means of the catalysts exhibiting excellent stereoselectivity. Besides their synthetic value, the nitrile-amide converting enzymes also play an important role in environmental protection. In this context, cloning of the genes and expression of these enzymes are presented. In the near future in China, an increasing number of novel nitrile-amide converting organisms will be screened and their potential in the synthesis of useful acids and amides will be further exploited.
Found
Are you a researcher?
Create a profile to get free access to personal recommendations for colleagues and new articles.