Lei S P, Lin H C, Wang S S, Higaki P, Wilcox G
Department of Microbiology, University of California, Los Angeles 90021.
Gene. 1992 Aug 1;117(1):119-24. doi: 10.1016/0378-1119(92)90499-f.
The peh gene, encoding polygalacturonase (Peh), was identified in Erwinia carotovora strain EC and cloned in Escherichia coli. Recombinant Peh (re-Peh) was purified from E. coli strain 706 containing peh on a recombinant plasmid. The activity of the re-Peh protein is optimal at pH 5.5. The N-terminal and internal amino acid (aa) sequences of re-Peh were determined and compared to the aa sequence deduced from the nucleotide (nt) sequence of the cloned peh. The re-Peh has no similarity, based on either the nt sequences or the deduced aa sequences, to pectate lyases from the same Er. carotovora strain or other organisms.
在胡萝卜软腐欧文氏菌菌株EC中鉴定出编码多聚半乳糖醛酸酶(Peh)的peh基因,并将其克隆到大肠杆菌中。从含有重组质粒上peh的大肠杆菌菌株706中纯化重组Peh(re-Peh)。re-Peh蛋白的活性在pH 5.5时最佳。测定了re-Peh的N端和内部氨基酸(aa)序列,并与从克隆的peh核苷酸(nt)序列推导的aa序列进行比较。基于nt序列或推导的aa序列,re-Peh与同一胡萝卜软腐欧文氏菌菌株或其他生物体的果胶酸裂解酶没有相似性。