Linton K J, Jarvis B W, Hutchinson C R
School of Pharmacy, University of Wisconsin, Madison 53706.
Gene. 1995 Feb 3;153(1):33-40. doi: 10.1016/0378-1119(94)00809-7.
Genes involved in deoxysugar metabolism, encoding thymidine diphospho (TDP)-glucose 4,6-dehydratase (gdh) and a putative TDP-4-keto-6-deoxyglucose 3,5-epimerase (kde), were cloned from the erythromycin (Er)-producing Saccharopolyspora erythraea by means of an oligodeoxynucleotide corresponding to a segment of the purified Gdh protein. Determination of the nucleotide sequence established that kde lies 3' to gdh. The function of gdh was confirmed by an enzymatic assay following expression of the gene in Escherichia coli. Southern analysis indicated that Sa. erythraea contains only one copy of gdh and kde. It was not possible to establish whether these genes are required for Er biosynthesis, but they appear to be essential for cellular metabolism, since resolution of a partial diploid containing a wt and a disrupted copy of gdh always maintained the wt gene. These loci do not lie within or near the known boundaries of the cluster of Er-production and -resistance genes, nor do they appear to be flanked by other deoxysugar biosynthesis genes.
通过与纯化的Gdh蛋白片段相对应的寡脱氧核苷酸,从产红霉素的糖多孢红霉菌中克隆出参与脱氧糖代谢的基因,这些基因编码胸苷二磷酸(TDP)-葡萄糖4,6-脱水酶(gdh)和一种假定的TDP-4-酮-6-脱氧葡萄糖3,5-表异构酶(kde)。核苷酸序列测定表明kde位于gdh的3'端。在大肠杆菌中表达该基因后,通过酶促测定证实了gdh的功能。Southern分析表明,糖多孢红霉菌仅含有一个gdh和kde拷贝。无法确定这些基因是否是红霉素生物合成所必需的,但它们似乎对细胞代谢至关重要,因为含有野生型和gdh破坏拷贝的部分二倍体的分离总是保留野生型基因。这些基因座不在红霉素产生和抗性基因簇的已知边界内或附近,它们似乎也没有被其他脱氧糖生物合成基因侧翼包围。