Biotechnological production of feed nucleotides by microbial strain improvement

被引:23
作者
Ledesma-Amaro, Rodrigo [1 ]
Jimenez, Alberto [1 ]
Santos, Maria A. [1 ]
Revuelta, Jose L. [1 ]
机构
[1] Univ Salamanca, Metab Engn Grp, Dept Microbiol & Genet, E-37007 Salamanca, Spain
关键词
Inosine monophosphate; Guanosine monophosphate; Purine biosynthesis; Flavour enhancers; Metabolic engineering; Feed nucleotides; Nucleotide production; Systems metabolic engineering; PURINE BIOSYNTHETIC-PATHWAY; ESCHERICHIA-COLI; BACILLUS-SUBTILIS; INOSINE ACCUMULATION; SACCHAROMYCES-CEREVISIAE; RIBOFLAVIN PRODUCTION; ASHBYA-GOSSYPII; CORYNEBACTERIUM-GLUTAMICUM; NUCLEOSIDE PHOSPHORYLASES; TRANSCRIPTION FACTOR;
D O I
10.1016/j.procbio.2013.06.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sodium salts of inosine monophosphate (IMP) and guanosine monophosphate (GMP) are potent flavour enhancers. They are widely used as food additives in combination with monosodium glutamate (MSG) to synergistically increase umami flavour. In recent years, both inosine and guanosine derivatives have gained further importance because of their beneficial effects, related to their antioxidant, neuroprotective, cardiotonic and immunomodulatory properties. The industrial production of both IMP and GMP is mainly achieved either by RNA breakdown and nucleotide extraction or by microbial fermentation using different microorganisms such as Corynebacterium, Bacillus, or Escherichia coli. This work reviews the metabolic pathways and regulatory networks of purine synthesis, including both IMP and GMP, and the biotechnological processes applied to the production of these compounds, ranging from classical random mutagenesis to rational design by metabolic engineering. Recent advances of systems biology approaches, along with the rapid development of synthetic biology, may offer a basis for future manipulations to further increase the productivity of the fermentation processes. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1263 / 1270
页数:8
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