Puyet A, Espinosa M
Centro de Investigaciones Biológicas, C.S.I.C., Madrid, Spain.
J Mol Biol. 1993 Apr 5;230(3):800-11. doi: 10.1006/jmbi.1993.1202.
The mechanism of induction of the maltose/maltodextrin regulon of the Gram-positive bacterium Streptococcus pneumoniae seems to be different to the positively controlled maltose regulons of the enteric bacteria Escherichia coli, Klebsiella pneumoniae and Salmonella typhimurium. In this work, we report on the structure of the S. pneumoniae genes involved in maltodextrin uptake malX, malC and malD. Comparisons of the amino acid sequences encoded by these genes indicate that they are homologous to the E. coli MalE periplasmic maltose binding protein and the two maltose permeases MalG and MalF. The analysis of transcription start points indicates that malXCD could be transcribed from a single consensus promoter sequence. Northern analysis of the mRNA molecules pertaining to this region reveals that the transcript encompassing all these three genes is apparently cleaved at a large putative mRNA secondary structure, yielding two mRNA molecules. The smaller of these molecules would include only the malX gene while a larger fragment spans through malC and malD. The processing of mRNA has not been reported in the Gram-negative maltose regulons, and may suggest either a less evolved or a divergent system for the control of gene expression of this regulon in S. pneumoniae.
革兰氏阳性菌肺炎链球菌麦芽糖/麦芽糊精调节子的诱导机制似乎与肠道细菌大肠杆菌、肺炎克雷伯菌和鼠伤寒沙门氏菌的正调控麦芽糖调节子不同。在这项研究中,我们报道了肺炎链球菌中参与麦芽糊精摄取的malX、malC和malD基因的结构。对这些基因编码的氨基酸序列进行比较表明,它们与大肠杆菌的周质麦芽糖结合蛋白MalE以及两种麦芽糖通透酶MalG和MalF同源。转录起始点分析表明,malXCD可能从一个单一的共有启动子序列转录。对该区域相关mRNA分子的Northern分析显示,包含所有这三个基因的转录本显然在一个大的假定mRNA二级结构处被切割,产生两个mRNA分子。其中较小的分子仅包含malX基因,而较大的片段跨越malC和malD。革兰氏阴性菌麦芽糖调节子中尚未报道mRNA的加工过程,这可能表明肺炎链球菌中该调节子的基因表达控制系统要么进化程度较低,要么存在差异。