Gagnon G, Vadeboncoeur C, Frenette M
Département de Biochimie (Sciences), Université Laval, Québec, Canada.
Gene. 1993 Dec 22;136(1-2):27-34. doi: 10.1016/0378-1119(93)90443-7.
The Streptococcus salivarius ptsH gene encoding histidine-containing phosphocarrier protein (HPr) of the phosphotransferase system (PTS) has been cloned, sequenced, and found to be part of a ptsH, ptsI operon. Upstream from ptsH, putative -35 and -10 boxes and a Shine-Dalgarno sequence highly similar to the Escherichia coli consensus regulatory elements were identified. A second promoter, located in the ptsH coding sequence was also observed and is sufficient for the expression of the S. salivarius ptsI gene, encoding enzyme I of the PTS in E. coli [Gagnon et al., Gene 121 (1992) 71-78]. The amino acid sequence of S. salivarius HPr, inferred from the ptsH sequence, shared identity varying between 37 and 76% with known HPr from other bacteria. Moreover, the S. salivarius HPr shared 78% identity with an HPr-like protein of Aspergillus fumigatus, a eukaroytic mold that does not possess a functional PTS. Expression analysis of S. salivarius HPr in E. coli demonstrated that (i) S. salivarius ptsH is expressed in E. coli under the control of its own promoter, (ii) S. salivarius HPr synthesized by E. coli is completely processed by methionine aminopeptidase, and (iii) S. salivarius HPr is phosphorylated in vivo by E. coli enzyme I. It was also observed that, in E. coli, the copy number of pUC18 bearing S. salivarius ptsH was reduced more than 25-fold, as compared to pUC18 without an insertion.
编码磷酸转移酶系统(PTS)含组氨酸的磷酸载体蛋白(HPr)的唾液链球菌ptsH基因已被克隆、测序,并发现它是ptsH、ptsI操纵子的一部分。在ptsH上游,鉴定出了与大肠杆菌共有调控元件高度相似的推定-35和-10框以及Shine-Dalgarno序列。还观察到位于ptsH编码序列中的第二个启动子,它足以驱动唾液链球菌ptsI基因的表达,该基因在大肠杆菌中编码PTS的酶I [加尼翁等人,《基因》121 (1992) 71 - 78]。从ptsH序列推断出的唾液链球菌HPr的氨基酸序列与其他细菌已知的HPr的同源性在37%至76%之间变化。此外,唾液链球菌HPr与烟曲霉的一种HPr样蛋白有78%的同源性,烟曲霉是一种不具有功能性PTS的真核霉菌。在大肠杆菌中对唾液链球菌HPr的表达分析表明:(i)唾液链球菌ptsH在其自身启动子的控制下在大肠杆菌中表达;(ii)大肠杆菌合成的唾液链球菌HPr被甲硫氨酸氨肽酶完全加工;(iii)唾液链球菌HPr在体内被大肠杆菌的酶I磷酸化。还观察到,在大肠杆菌中,携带唾液链球菌ptsH的pUC18的拷贝数与未插入片段的pUC18相比减少了25倍以上。