Nicholls D J, Sundaram T K, Atkinson T, Minton N P
Division of Biotechnology, Centre for Applied Microbiology and Research, Porton, Salisbury, U.K.
FEMS Microbiol Lett. 1990 Jun 15;58(1):7-14. doi: 10.1016/0378-1097(90)90093-6.
A 3 kb DNA fragment containing the gene (mdh) encoding malate dehydrogenase (MDH) from the thermophile Thermus aquaticus B was cloned in Escherichia coli and its nucleotide sequence determined. Comparative analysis showed the nucleotide sequence to be very closely related to that determined for the Thermus flavus mdh gene and flanking regions, with no differences between the predicted amino acid sequences of the MDHs. A proximal open reading frame, identified as the sucD gene, and the mdh gene may be parts of the same operon in T. aquaticus B. Expression of the T. aquaticus B mdh gene in E. coli was found to be at a relatively low level. A simple method for purification of thermostable MDH from the E. coli clone containing the T. aquaticus B mdh gene is presented.
从嗜热栖热菌B中克隆出一个包含编码苹果酸脱氢酶(MDH)的基因(mdh)的3 kb DNA片段,并将其克隆到大肠杆菌中,测定了其核苷酸序列。比较分析表明,该核苷酸序列与黄栖热菌mdh基因及其侧翼区域的测定序列非常相似,MDH的预测氨基酸序列之间没有差异。一个被鉴定为sucD基因的近端开放阅读框和mdh基因可能是嗜热栖热菌B中同一个操纵子的组成部分。发现嗜热栖热菌B的mdh基因在大肠杆菌中的表达水平相对较低。本文介绍了一种从含有嗜热栖热菌B mdh基因的大肠杆菌克隆中纯化热稳定MDH的简单方法。