Brünker P, Altenbuchner J, Mattes R
Institut für Industrielle Genetik, Universität Stuttgart, Germany.
Gene. 1998 Jan 5;206(1):117-26. doi: 10.1016/s0378-1119(97)00574-x.
A DNA fragment from Pseudomonas fluorescens DSM50106 containing the genes for the uptake and utilization of mannitol, arabitol and glucitol was cloned in Escherichia coli and sequenced. Seven open reading frames (mtlEFGKDYZ) were identified on the 10031 bp fragment. The deduced amino acid sequences of the first four open reading frames (mtlEFGK) revealed significant similarity to the components of the maltose transport system in E. coli and Salmonella typhimurium. The gene mtlD encoding a polyol dehydrogenase was located downstream of mtlK. The deduced proteins of the last two genes on the fragment showed a high similarity to a fructokinase from Vibrio alginolyticus (MtlZ) and a xylulose kinase from Streptomyces rubiginosus (MtlY), respectively. Both genes were expressed in E. coli. MtlZ phosphorylated fructose, glucose and glucitol whereas MtlY was highly specific for xylulose. Upstream of mtlE, a putative promoter/operator region was identified by promoter probe studies which was active in P. fluorescens but not in E. coli.
从荧光假单胞菌DSM50106中分离出一段包含甘露醇、阿拉伯糖醇和葡糖醇摄取与利用相关基因的DNA片段,将其克隆到大肠杆菌中并进行测序。在这个10031 bp的片段上鉴定出7个开放阅读框(mtlEFGKDYZ)。前四个开放阅读框(mtlEFGK)推导的氨基酸序列与大肠杆菌和鼠伤寒沙门氏菌中麦芽糖转运系统的组分具有显著相似性。编码多元醇脱氢酶的基因mtlD位于mtlK的下游。该片段上最后两个基因推导的蛋白质分别与溶藻弧菌的果糖激酶(MtlZ)和微红链霉菌的木酮糖激酶(MtlY)高度相似。这两个基因都在大肠杆菌中表达。MtlZ可磷酸化果糖、葡萄糖和葡糖醇,而MtlY对木酮糖具有高度特异性。在mtlE上游,通过启动子探针研究鉴定出一个假定的启动子/操纵子区域,该区域在荧光假单胞菌中具有活性,但在大肠杆菌中无活性。