Debottlenecking the 1,3-propanediol pathway by metabolic engineering

被引:138
作者
Celinska, E. [1 ]
机构
[1] Poznan Univ Life Sci, Dept Biotechnol & Food Microbiol, PL-60627 Poznan, Poland
关键词
1,3-propanediol; Metabolic engineering; Bio-based chemical; White biotechnology; B-12-DEPENDENT GLYCEROL DEHYDRATASE; ADENOSYLCOBALAMIN-DEPENDENT DIOL; CLOSTRIDIUM-BUTYRICUM DSM-5431; ANAEROBIC CONTINUOUS-CULTURE; MICRO-AEROBIC CONDITIONS; PNEUMONIAE-DHA REGULON; FED-BATCH FERMENTATION; KLEBSIELLA-PNEUMONIAE; ESCHERICHIA-COLI; CITROBACTER-FREUNDII;
D O I
10.1016/j.biotechadv.2010.03.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The history of 1,3-propanediol (1,3-PD) conversion from being a specialty chemical to being a bulk chemical illustrates that the concerted effort of different metabolic engineering approaches brings the most successful results. In order to metabolically tailor the 1,3-PD production pathway multiple strategies have been pursued. Knocking-out genes responsible for by-products formation, intergeneric transfer and over-expression of the genes directly involved in the pathway, manipulation with internal redox balance, introduction of a synthetic flux control point, and modification of the substrate mechanism of transport are some of the strategies applied. The metabolic engineering of the microbial 1,3-PD production exploits both native producers and microorganisms with acquired ability to produce the diol via genetic manipulations. Combination of the appropriate genes from homologous and heterologous hosts is expected to bring a desired objective of production of 1,3-PD cheaply, efficiently and independently from non-renewable resources. The state-of-the-art of the 1,3-PD pathway metabolic engineering is reviewed in this paper. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:519 / 530
页数:12
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