Rioux C R, Kadner R J
Department of Microbiology, School of Medicine, University of Virginia, Charlottesville 22908.
Mol Gen Genet. 1989 Jun;217(2-3):301-8. doi: 10.1007/BF02464897.
Transport of vitamin B12 across the cytoplasmic membrane of Escherichia coli requires the products of btuC and btuD, two genes in the btuCED operon. The role of btuE, the central gene of this operon, was examined. Deletions within btuE were constructed by removal of internal restriction fragments and were crossed onto the chromosome by allelic replacement. In-frame deletions that removed 20% or 82% of the btuE coding region did not affect expression of the distal btuD gene. These nonpolar deletions had little effect on vitamin B12 binding (whole cells or periplasmic fraction) and transport. They did not affect the utilization of vitamin B12 or other cobalamins for methionine biosynthesis, even in strains with decreased outer membrane transport of vitamin B12. The btuE mutations did not impair adenosyl-cobalamin dependent catabolism of ethanolamine or repression of btuB expression. Thus, despite its genetic location in the transport operon, the btuE product plays no essential role in vitamin B12 transport.
维生素B12穿过大肠杆菌细胞质膜的运输需要btuCED操纵子中的两个基因btuC和btuD的产物。对该操纵子的中心基因btuE的作用进行了研究。通过去除内部限制片段构建了btuE内的缺失,并通过等位基因替换将其转移到染色体上。去除btuE编码区20%或82%的框内缺失不影响远端btuD基因的表达。这些非极性缺失对维生素B12结合(全细胞或周质部分)和运输影响很小。它们不影响维生素B12或其他钴胺素用于甲硫氨酸生物合成,即使在维生素B12外膜运输减少的菌株中也是如此。btuE突变不损害乙醇胺的腺苷钴胺素依赖性分解代谢或btuB表达的抑制。因此,尽管btuE产物在遗传上位于运输操纵子中,但它在维生素B12运输中不发挥重要作用。