Murphy N B, McConnell D J, Schwarz T F
J Bacteriol. 1987 Jan;169(1):334-9. doi: 10.1128/jb.169.1.334-339.1987.
The structural gene (zwf) for Leuconostoc mesenteroides glucose-6-phosphate dehydrogenase has been cloned into Escherichia coli on pBR322 by selecting for complementation of a zwf mutation of E. coli which eliminates glucose-6-phosphate dehydrogenase. The gene has been subcloned on a 3.4-kilobase DNA segment. The encoded glucose-6-phosphate dehydrogenase displays the dual nucleotide specificity (reacting with NAD and NADP) of the L. mesenteroides enzyme and has a subunit Mr of 55,000. A second gene encoding protein of subunit Mr 24,000 is also encoded on the 3.4-kilobase DNA segment. The genes have been located by the analysis of deletions and insertions generated in vitro and by transcriptional mapping with a promoterless chloramphenicol acetyl transferase cartridge inserted at different sites in the 3.4-kilobase fragment.
通过选择对消除6-磷酸葡萄糖脱氢酶的大肠杆菌zwf突变进行互补,将嗜热栖热放线菌6-磷酸葡萄糖脱氢酶的结构基因(zwf)克隆到大肠杆菌的pBR322上。该基因已亚克隆到一个3.4千碱基的DNA片段上。编码的6-磷酸葡萄糖脱氢酶表现出嗜热栖热放线菌酶的双核苷酸特异性(与NAD和NADP反应),亚基Mr为55,000。在3.4千碱基的DNA片段上还编码了一个编码亚基Mr为24,000的蛋白质的第二个基因。通过分析体外产生的缺失和插入以及用无启动子氯霉素乙酰转移酶盒在3.4千碱基片段的不同位点进行转录图谱分析来定位这些基因。