摘要
利用Red同源重组技术,快速敲除肺炎克雷伯氏菌中的编码D-乳酸脱氢酶的两个基因——ldhA和dld,获得KG1-1和KG1-2两个突变株,并研究了敲除编码D-乳酸脱氢酶基因丧失合成D-乳酸的KG1-1菌株的1,3-PD产量和菌体生长变化,实验结果表明乳酸合成缺失对现有工艺1,3-丙二醇发酵无影响。
The impact of blocking D-lactate formation by direct knocking out the genes of D-lactic dehydrogenase in Klebsiella pneumoniae was investigated. The two genes of ldhA and dld were knocked out separately to construct two mutants of KG1-1 and KG1-2. The results showed that KGI-1 was a D-lactate deficient mutant, while its 1,3-PD production and cell growth were not influenced on the present technology.
出处
《工业微生物》
CAS
CSCD
2014年第4期24-27,共4页
Industrial Microbiology