Kadner R J, Liggins G L
J Bacteriol. 1973 Aug;115(2):514-21. doi: 10.1128/jb.115.2.514-521.1973.
The chromosomal location of two genetic loci involved in the transport of cyanocobalamin (B(12)) in Escherichia coli K-12 was determined. One gene, btuA, is believed to code for the transport protein in the cytoplasmic membrane, because a mutant with an alteration in this gene has lost the ability to accumulate B(12) within the cell although normal levels of the surface receptors for B(12) are present. The other locus, btuB, apparently codes for the surface receptor on the outer membrane. These mutants have lost the ability to bind B(12) and have greatly reduced transport activity, although growth experiments have shown that they can utilize B(12) for growth, but with decreased efficiency. This surface receptor for B(12) also appears to function as the receptor for the E colicins, because btuB mutants are resistant to the E colicins, and mutants selected for resistance to colicin E1 are defective in B(12) binding and transport. The gene order was determined by transduction analysis to be cyc-argH-btuA-btuB-rif-purD. In addition, mutations in metH, the gene for the B(12)-dependent homocysteine methylating enzyme, were obtained in this study. This gene was localized between metA and malB.
确定了大肠杆菌K-12中参与钴胺素(B₁₂)转运的两个基因位点的染色体定位。一个基因btuA被认为编码细胞质膜中的转运蛋白,因为该基因发生改变的突变体已失去在细胞内积累B₁₂的能力,尽管存在正常水平的B₁₂表面受体。另一个位点btuB显然编码外膜上的表面受体。这些突变体已失去结合B₁₂的能力,并且转运活性大大降低,尽管生长实验表明它们可以利用B₁₂进行生长,但效率降低。这种B₁₂表面受体似乎也作为大肠杆菌素的受体发挥作用,因为btuB突变体对大肠杆菌素具有抗性,并且为抗大肠杆菌素E1而选择的突变体在B₁₂结合和转运方面存在缺陷。通过转导分析确定基因顺序为cyc-argH-btuA-btuB-rif-purD。此外,在本研究中获得了依赖B₁₂的同型半胱氨酸甲基化酶基因metH的突变。该基因定位于metA和malB之间。