Wu Shimei, Zheng Rikuan, Sha Zhenxia, Sun Chaomin
College of Life Sciences, Qingdao University, Qingdao 266071, China.
Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China.
Mar Drugs. 2017 Jul 10;15(7):218. doi: 10.3390/md15070218.
273 is a marine bacterium producing exopolysaccharide 273 (EPS273) with high anti-biofilm activity against PAO1. Here, the complete genome of 273 was sequenced and the genome contained a circular 5.03 Mb chromosome. With extensive analysis of the genome, a genetic locus containing 18 genes was predicted to be involved in the biosynthesis of EPS273. In order to confirm this prediction, two adjacent genes ( and ) encoding glycosyltransferases and one gene () encoding tyrosine protein kinase within the genetic locus were deleted and biosynthesis of EPS273 was checked in parallel. The molecular weight profile of EPS purified from the mutant Δ was obviously different from that purified from wild-type 273, while the corresponding EPS was hardly detected from the mutant Δ, which indicated the involvement of the proposed 18-gene cluster in the biosynthesis of EPS273. Moreover, the mutant Δ had the biofilm formed earlier compared with the wild type, and the mutant Δ almost completely lost the ability of biofilm formation. Therefore, EPS273 might facilitate the biofilm formation for its producing strain 273 while inhibiting the biofilm formation of PAO1. This study can contribute to better understanding of the biosynthesis of EPS273 and disclose the biological function of EPS273 for its producing strain 273.
273是一种海洋细菌,可产生对铜绿假单胞菌PAO1具有高抗生物膜活性的胞外多糖273(EPS273)。在此,对273的全基因组进行了测序,该基因组包含一条5.03 Mb的环状染色体。通过对该基因组的广泛分析,预测一个包含18个基因的基因座参与EPS273的生物合成。为了证实这一预测,删除了该基因座内两个相邻的编码糖基转移酶的基因(和)以及一个编码酪氨酸蛋白激酶的基因(),并同时检测了EPS273的生物合成。从突变体Δ中纯化的EPS的分子量图谱与从野生型273中纯化的明显不同,而从突变体Δ中几乎检测不到相应的EPS,这表明所提出的18基因簇参与了EPS273的生物合成。此外,与野生型相比,突变体Δ形成生物膜的时间更早,而突变体Δ几乎完全丧失了生物膜形成能力。因此,EPS273可能促进其产生菌株273的生物膜形成,同时抑制PAO1的生物膜形成。本研究有助于更好地理解EPS273的生物合成,并揭示EPS273对其产生菌株273的生物学功能。