Potrykus Joanna, Wegrzyn Grzegorz
Laboratory of Molecular Genetics, Department of Molecular Biology, University of Gdańsk, Kładki 24, 80-822 Gdańsk, Poland.
FEMS Microbiol Lett. 2004 Jun 15;235(2):265-71. doi: 10.1016/j.femsle.2004.04.041.
In Escherichia coli, the synthesis of colanic acid, an extracellular polysaccharide imminent in biofilm development, is a complicated process involving numerous genes and not yet wholly elucidated. Using a plasmid-borne E. coli K-12 gene library, we have identified a clone whose presence conferred mucoid colony phenotype onto E. coli CM2555 strain. Our results indicate that overexpression of a gene previously catalogued as ypdI, which encodes a putative lipoprotein, is responsible for this phenotype. We show that the mucoidy of ypdI -overexpressing bacteria is due to increased production of colanic acid. This phenotype depends on the function of the rcsA gene, but not on that of rcsF. These results suggest that the ypdI gene product might be an additional factor playing a role in colanic acid synthesis, indicating that this process can be even more complicated than supposed to date. However, no obvious phenotype was observed in the DeltaypdI::kan mutant cultivated under standard laboratory conditions.
在大肠杆菌中,合成胞外多糖——在生物膜形成过程中至关重要的柯烷酸,是一个涉及众多基因的复杂过程,目前尚未完全阐明。利用携带质粒的大肠杆菌K-12基因文库,我们鉴定出一个克隆,其存在赋予了大肠杆菌CM2555菌株黏液样菌落表型。我们的结果表明,先前归类为ypdI的基因(该基因编码一种假定的脂蛋白)的过表达导致了这种表型。我们发现,过表达ypdI的细菌产生黏液是由于柯烷酸产量增加。这种表型取决于rcsA基因的功能,而不取决于rcsF基因的功能。这些结果表明,ypdI基因产物可能是在柯烷酸合成中发挥作用的另一个因素,这表明该过程可能比迄今认为的更为复杂。然而,在标准实验室条件下培养的DeltaypdI::kan突变体中未观察到明显的表型。