Du Chenyu, Zhang Yanping, Li Yin, Cao Zhu'an
Institute of Biochemical Engineering, Department of Chemical Engineering, Tsinghua University, Beijing 100084, People's Republic of China.
Appl Environ Microbiol. 2007 Jul;73(14):4515-21. doi: 10.1128/AEM.02857-06. Epub 2007 May 18.
This report describes a novel redox potential (oxidoreduction potential [ORP])-based screening strategy for the isolation of mutants of Klebsiella pneumoniae which have an increased ability to produce 1,3-propanediol (1,3-PD). This method can be described as follows: first, to determine an ORP range which is preferred for the wild-type strain to grow and to produce 1,3-PD; second, to subject a chemically mutagenized culture to a reduced ORP level which is deleterious for the wild-type strain. Colonies that showed high specific growth rates at deleterious ORP levels were selected, and their abilities to produce 1,3-PD were investigated. In an ORP-based screening experiment where the ORP was controlled at -280 mV, 4 out of 11 isolated strains were recognized as positive mutant strains. A mutant which is capable of producing higher concentrations of 1,3-PD was subjected to fed-batch fermentations for further characterization. Its preferred ORP level (-280 mV) was significantly lower than that of its parent (-190 mV). The highest 1,3-PD concentration of the mutant was 915 mmol liter(-1), which was 63.1% higher than that of the parent. Metabolic-flux analysis suggested that the intracellular reductive branch of the mutant was strengthened, which improved 1,3-PD biosynthesis. The procedure and results presented here provide a novel method of screening for strains with improved product formation.
本报告描述了一种基于新型氧化还原电位(ORP)的筛选策略,用于分离肺炎克雷伯菌中具有更高1,3 - 丙二醇(1,3 - PD)生产能力的突变体。该方法可描述如下:首先,确定野生型菌株生长和生产1,3 - PD的最佳ORP范围;其次,将化学诱变后的培养物置于对野生型菌株有害的较低ORP水平下。选择在有害ORP水平下显示出高比生长速率的菌落,并研究它们生产1,3 - PD的能力。在ORP控制在 - 280 mV的基于ORP的筛选实验中,11株分离菌株中有4株被鉴定为阳性突变菌株。对能够产生更高浓度1,3 - PD的突变体进行补料分批发酵以进一步表征。其最佳ORP水平( - 280 mV)明显低于其亲本( - 190 mV)。该突变体的最高1,3 - PD浓度为915 mmol·L⁻¹,比其亲本高63.1%。代谢通量分析表明,该突变体的细胞内还原分支得到加强,从而改善了1,3 - PD的生物合成。本文介绍的方法和结果提供了一种筛选具有改善产物形成能力菌株的新方法。