Tsoi T V, Zaitsev G M, Plotnikova E G, Kosheleva I A, Boronin A M
Institute of Biochemistry and Physiology of Microorganisms, U.S.S.R. Academy of Sciences, Moscow.
FEMS Microbiol Lett. 1991 Jun 15;65(2):165-9. doi: 10.1016/0378-1097(91)90298-o.
The fsbA gene controlling the first step of 4-chlorobenzoic acid (4CBA) metabolism in the Gram-positive soil bacterium Arthrobacter globiformis KZT1 has been cloned and analysed in Escherichia coli. The E. coli minicells analysis showed that a polypeptide(s) with Mr = 58 kDa (and/or Mr = 32 kDa) can be the fcbA product(s). Despite the gene dose amplification and control of the E. coli inducible Plac promoter, the level of functional expression of the fcbA gene in E. coli cells seems comparable only with that in the parental KZT1 strain. Effective 4CBA dechlorination by recombinant cells during growth in the presence of substrate within a range of concentrations 0.1 g/l to 0.7 g/l as well as a sudden reduction in the reaction efficiency at higher substrate concentrations were observed.
控制革兰氏阳性土壤细菌球形节杆菌KZT1中4-氯苯甲酸(4CBA)代谢第一步的fsbA基因已在大肠杆菌中克隆并分析。大肠杆菌小细胞分析表明,分子量为58 kDa(和/或32 kDa)的一种或多种多肽可能是fcbA产物。尽管进行了基因剂量扩增并控制了大肠杆菌的可诱导Plac启动子,但fcbA基因在大肠杆菌细胞中的功能表达水平似乎仅与亲本KZT1菌株相当。在0.1 g/l至0.7 g/l浓度范围内的底物存在下生长期间,观察到重组细胞对4CBA的有效脱氯作用,以及在较高底物浓度下反应效率的突然降低。