Ishige K, Kameda A, Noguchi T, Shiba T
Biochemicals Division, YAMASA Corporation, Choshi, Chiba, Japan.
DNA Res. 1998 Jun 30;5(3):157-62. doi: 10.1093/dnares/5.3.157.
We have cloned and sequenced a gene encoding polyphosphate kinase (PPK) from Pseudomonas aeruginosa PAO1. The gene immediately follows the hemB gene encoding porphobilinogen synthase responsible for heme synthesis. The predicted amino acid sequence of P. aeruginosa PPK is similar to those of PPKs previously characterized except that it possesses an extra stretch of 46 amino acids at its N-terminus, which has significant similarity to the Ras-related protein ARA5 of Arabidopsis thaliana. When P. aeruginosa PPK was overproduced in Escherichia coli, ATP-dependent polyphosphate-synthesizing activity was drastically enhanced, confirming that the protein is a PPK.
我们已经克隆并测序了来自铜绿假单胞菌PAO1的编码多聚磷酸激酶(PPK)的基因。该基因紧接着编码负责血红素合成的胆色素原合酶的hemB基因。铜绿假单胞菌PPK的预测氨基酸序列与先前鉴定的PPK序列相似,只是在其N端有一段额外的46个氨基酸的延伸,这与拟南芥的Ras相关蛋白ARA5有显著的相似性。当铜绿假单胞菌PPK在大肠杆菌中过量表达时,ATP依赖性多聚磷酸合成活性急剧增强,证实该蛋白是一种PPK。