Weissborn A C, Liu Q, Rumley M K, Kennedy E P
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115.
J Bacteriol. 1994 May;176(9):2611-8. doi: 10.1128/jb.176.9.2611-2618.1994.
The galU gene of Escherichia coli, thought to encode the enzyme UTP:alpha-D-glucose-1-phosphate uridylyltransferase, had previously been mapped to the 27-min region of the chromosome (J. A. Shapiro, J. Bacteriol. 92:518-520, 1966). By complementation of the membrane-derived oligosaccharide biosynthetic defect of strains with a galU mutation, we have now identified a plasmid containing the galU gene and have determined the nucleotide sequence of this gene. The galU gene is located immediately downstream of the hns gene, and its open reading frame would be transcribed in the direction opposite that of the hns gene (i.e., clockwise on the E. coli chromosome). The nucleotide sequences of five galU mutations were also determined. The enzyme UTP:alpha-D-glucose-1-phosphate uridylyltransferase was purified from a strain containing the galU gene on a multicopy plasmid. The amino-terminal amino acid sequence (10 residues) of the purified enzyme was identical to the predicted amino acid sequence (after the initiating methionine) of the galU-encoded open reading frame. The functional enzyme appears to be a tetramer of the galU gene product.
大肠杆菌的galU基因,之前被认为编码UTP:α-D-葡萄糖-1-磷酸尿苷酰转移酶,此前已被定位到染色体的27分钟区域(J. A. Shapiro,《细菌学杂志》92:518 - 520,1966年)。通过对具有galU突变的菌株的膜衍生寡糖生物合成缺陷进行互补,我们现在鉴定出了一个含有galU基因的质粒,并确定了该基因的核苷酸序列。galU基因位于hns基因的紧邻下游,其开放阅读框的转录方向与hns基因相反(即在大肠杆菌染色体上为顺时针方向)。还确定了五个galU突变的核苷酸序列。从一个在多拷贝质粒上含有galU基因的菌株中纯化出了UTP:α-D-葡萄糖-1-磷酸尿苷酰转移酶。纯化酶的氨基末端氨基酸序列(10个残基)与galU编码的开放阅读框的预测氨基酸序列(起始甲硫氨酸之后)相同。功能性酶似乎是galU基因产物的四聚体。