VanWagoner Timothy M, Whitby Paul W, Morton Daniel J, Seale Thomas W, Stull Terrence L
Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104, USA.
J Bacteriol. 2004 Oct;186(19):6409-21. doi: 10.1128/JB.186.19.6409-6421.2004.
Haemophilus influenzae is one of a growing number of bacteria in which the natural ability to uptake exogenous DNA for potential genomic transformation has been recognized. To date, several operons involved in transformation in this organism have been described. These operons are characterized by a conserved 22-bp regulatory element upstream of the first gene and are induced coincident with transfer from rich to nutrient-depleted media. The previously identified operons comprised genes encoding proteins that include members of the type II secretion system and type IV pili, shown to be essential for transformation in other bacteria, and other proteins previously identified as required for transformation in H. influenzae. In the present study, three novel competence operons were identified by comparative genomics and transcriptional analysis. These operons have been further characterized by construction of null mutants and examination of the resulting transformation phenotypes. The putative protein encoded by the HI0366 gene was shown to be essential for DNA uptake, but not binding, and is homologous to a protein shown to be required for pilus biogenesis and twitching motility in Pseudomonas aeruginosa. An insertion in HI0939 abolished both DNA binding and uptake. The predicted product of this gene shares characteristics with PulJ, a pseudopilin involved in pullulanase export in Klebsiella oxytoca.
流感嗜血杆菌是越来越多的细菌之一,其摄取外源DNA进行潜在基因组转化的天然能力已得到认可。迄今为止,已描述了该生物体中几个参与转化的操纵子。这些操纵子的特征是第一个基因上游有一个保守的22个碱基对的调控元件,并在从丰富培养基转移到营养耗尽培养基时被诱导。先前鉴定的操纵子包含编码蛋白质的基因,这些蛋白质包括II型分泌系统和IV型菌毛的成员,已证明它们对其他细菌的转化至关重要,以及先前鉴定为流感嗜血杆菌转化所需的其他蛋白质。在本研究中,通过比较基因组学和转录分析鉴定了三个新的感受态操纵子。通过构建缺失突变体并检查产生的转化表型,对这些操纵子进行了进一步表征。HI0366基因编码的推定蛋白质被证明对DNA摄取至关重要,但对结合不重要,并且与铜绿假单胞菌中菌毛生物合成和颤动运动所需的一种蛋白质同源。HI0939中的插入消除了DNA结合和摄取。该基因的预测产物与PulJ具有共同特征,PulJ是一种参与产酸克雷伯菌中支链淀粉酶输出的假菌毛蛋白。