Lee Seung-Jin, Song Ok-Ryul, Lee Young-Choon, Choi Yong-Lark
Division of Biotechnology, Faculty of Natural Resources and Life Science, Dong-A University, Busan 604-714, Korea.
Biotechnol Lett. 2003 Feb;25(3):191-7. doi: 10.1023/a:1022386514487.
To understand the mechanism of phosphate accumulation, a gene encoding polyphosphate kinase (PPK) was cloned from the genomic library of Serratia marcescens by Southern hybridization. From the nucleotide sequence of a 4 kb DNA fragment, an open reading frame of 2063 nucleotides was identified encoding a protein of 686 amino acids with molecular mass of 70 kDa. The potential CRP binding site and pho box sequence were found upstream of the putative promoter in the regulatory region. The expression of PPK resulted in the formation of inclusion bodies and the product was active at low temperature. The E. coli strain harboring plasmid pSPK5 with ppk gene increased enzyme activity of polyphosphate kinase, resulting in increased accumulation of polyphosphate in E. coli.
为了解磷酸盐积累的机制,通过Southern杂交从粘质沙雷氏菌的基因组文库中克隆了一个编码多聚磷酸激酶(PPK)的基因。从一个4 kb DNA片段的核苷酸序列中,鉴定出一个2063个核苷酸的开放阅读框,其编码一个686个氨基酸、分子量为70 kDa的蛋白质。在调控区推定的启动子上游发现了潜在的CRP结合位点和pho盒序列。PPK的表达导致包涵体的形成,并且该产物在低温下具有活性。携带含有ppk基因的质粒pSPK5的大肠杆菌菌株增加了多聚磷酸激酶的酶活性,导致大肠杆菌中多聚磷酸盐的积累增加。