Shen Pei-Hong, Wu Bo
The Key Laboratory of Ministry of Education for Microbial and Plant Genetic Engineering, The College of Life Science and Technology, Guangxi University, 100 Daxue Road, Nanning, Guangxi, China.
J Ind Microbiol Biotechnol. 2007 Oct;34(10):657-63. doi: 10.1007/s10295-007-0238-0. Epub 2007 Jul 25.
Methylobacterium sp. MB200 capable of producing glyoxylate from methanol was obtained by enrichment culture using a medium containing methanol as the sole carbon source. A hpr gene that encodes a hydroxypyruvate reductase (HPR) was cloned from this strain and was ligated into the vector pLAFR3 to obtain the recombinant plasmid pLAFRh, which was transferred into M. sp. MB200 to generate an recombinant strain MB201. Homologous expression of hpr under the control of the lacZ promoter led to the enhanced glyoxylate accumulation in cultures of Methylobacterium sp MB201. The yield of glyoxylate reached 14.38 mg/mL, representing nearly a twofold increase when compared with the wild-type strain.
通过使用以甲醇作为唯一碳源的培养基进行富集培养,获得了能够从甲醇生产乙醛酸的甲基杆菌属MB200菌株。从该菌株中克隆了一个编码羟基丙酮酸还原酶(HPR)的hpr基因,并将其连接到载体pLAFR3中,以获得重组质粒pLAFRh,将其转入甲基杆菌属MB200中以产生重组菌株MB201。在lacZ启动子控制下hpr的同源表达导致甲基杆菌属MB201培养物中乙醛酸积累增加。乙醛酸产量达到14.38 mg/mL,与野生型菌株相比几乎增加了两倍。