Sharma V, Suvarna K, Meganathan R, Hudspeth M E
Department of Biological Sciences, Northern Illinois University, DeKalb 60115-2861.
J Bacteriol. 1992 Aug;174(15):5057-62. doi: 10.1128/jb.174.15.5057-5062.1992.
In Escherichia coli, the biosynthesis of the electron carrier menaquinone (vitamin K2) involves at least seven identified enzymes. One of these, naphthoate synthase, forms the bicyclic ring system by catalyzing the conversion of o-succinylbenzoyl-coenzyme A to 1,4-dihydroxy-2-naphthoic acid. The gene for this enzyme has been previously identified as menB. By genetic and biochemical tests, a 1.349-kb DNA fragment from the E. coli men locus complements menB mutants. This fragment contains a single 285-codon open reading frame (ORF). Recombinant plasmids containing deletions of either the amino or the carboxy region of the ORF fail to complement the mutants. The ORF is preceded by consensus sequences for a ribosomal binding site and a sigma 70 promoter. menB transcription sufficient to complement the menB mutant in vivo and in vitro can be initiated from the identified putative promoter, and that in the constructs, menB expression, can be made independent of read-through transcription from the lac promoter. However, multicopy plasmids containing menB fail to generate the expected levels of enzymatic activity.
在大肠杆菌中,电子载体甲萘醌(维生素K2)的生物合成涉及至少七种已确定的酶。其中之一,萘酸盐合酶,通过催化邻琥珀酰苯甲酸辅酶A转化为1,4 - 二羟基 - 2 - 萘甲酸形成双环系统。该酶的基因先前已被鉴定为menB。通过遗传和生化测试,来自大肠杆菌men基因座的一个1.349 kb的DNA片段可互补menB突变体。该片段包含一个单一的285密码子开放阅读框(ORF)。含有ORF氨基或羧基区域缺失的重组质粒无法互补突变体。该ORF之前有核糖体结合位点和σ70启动子的共有序列。足以在体内和体外互补menB突变体的menB转录可以从已确定的推定启动子起始,并且在构建体中,menB表达可以独立于来自lac启动子的通读转录。然而,含有menB的多拷贝质粒未能产生预期水平的酶活性。