Old I G, Margarita D, Glass R E, Saint Girons I
Unité des Leptospires, Institut Pasteur, Paris, France.
Gene. 1990 Mar 1;87(1):15-21. doi: 10.1016/0378-1119(90)90490-i.
The Escherichia coli K-12 metH gene, encoding the vitamin B12-dependent homocysteine transmethylase, is located between iclR and lysC in the 91-min region of the chromosome. The metH gene has been sequenced and reveals an open reading frame of 3600 bp encoding a polypeptide of 1200 amino acids (aa) with a calculated Mr of 132 628. The first 414 aa of the deduced polypeptide sequence are 92% identical to the 414 aa deduced from the partially sequenced Salmonella typhimurium LT2 metH gene. In-frame fusions of metH to lacZ were used to confirm the reading frame of the metH gene and to study its regulation. metH was repressed tenfold, presumably indirectly, by L-methionine and the metJ gene product, while vitamin B12 did not induce de novo synthesis of MetH.
编码依赖维生素B12的同型半胱氨酸转甲基酶的大肠杆菌K-12 metH基因,位于染色体91分钟区域的iclR和lysC之间。metH基因已被测序,显示有一个3600 bp的开放阅读框,编码一个1200个氨基酸(aa)的多肽,计算的分子量为132628。推导的多肽序列的前414个氨基酸与从部分测序的鼠伤寒沙门氏菌LT2 metH基因推导的414个氨基酸有92%的同一性。metH与lacZ的读框内融合用于确认metH基因的阅读框并研究其调控。L-甲硫氨酸和metJ基因产物可使metH表达量被抑制10倍,推测为间接抑制,而维生素B12不会诱导MetH的从头合成。