Han Feng, Li Meng, Lin Hong, Wang Jingxue, Cao Limin, Khan Muhammad Naseem
Food Safety Laboratory, Ocean University of China, Qingdao, 266003, People's Republic of China.
J Ind Microbiol Biotechnol. 2014 Jun;41(6):1017-26. doi: 10.1007/s10295-014-1438-z. Epub 2014 Apr 17.
Shewanella putrefaciens has been identified as a specific spoilage organism commonly found in chilled fresh fish, which contributes to the spoilage of fish products. Limiting S. putrefaciens growth can extend the shelf-life of chilled fish. Endolysins, which are lytic enzymes produced by bacteriophages, have been considered an alternative to control bacterial growth, and have been useful in various applications, including food preservation. We report here, for the first time, the complete genome sequence of a novel phage Spp001, which lyses S. putrefaciens Sp225. The Spp001 genome comprises a 54,789-bp DNA molecule with 67 open reading frames and an average total G + C content of 49.42 %. In silico analysis revealed that the Spp001 open reading frames encode various putative functional proteins, including an endolysin (ORF 62); however, no sequence for genes encoding the holin polypeptides, which work in concert with endolysins, was identified. To examine further the lytic activity of Spp001, we analyzed the lytic enzyme-containing fraction from phages released at the end of the phage lytic cycle in S. putrefaciens, using diffusion and turbidimetric assays. The results show that the partially purified extract contained endolysin, as indicated by a high hydrolytic activity towards bacterial peptidoglycan decrease in the OD590 value by 0.160 in 15 min. The results will allow further investigation of the purification of natural Spp001 endolysin, the extension of Spp001 host range, and the applications of the phage-encoded enzymes.
腐败希瓦氏菌已被确定为冷藏鲜鱼中常见的一种特定腐败菌,它会导致鱼产品变质。限制腐败希瓦氏菌的生长可以延长冷藏鱼的货架期。内溶素是噬菌体产生的裂解酶,已被视为控制细菌生长的一种替代方法,并已在包括食品保鲜在内的各种应用中发挥作用。我们在此首次报告一种新型噬菌体Spp001的完整基因组序列,该噬菌体可裂解腐败希瓦氏菌Sp225。Spp001基因组由一个54,789碱基对的DNA分子组成,有67个开放阅读框,平均总G + C含量为49.42%。计算机分析表明,Spp001的开放阅读框编码各种推定的功能蛋白,包括一种内溶素(开放阅读框62);然而,未鉴定出与内溶素协同作用的编码孔蛋白多肽的基因序列。为了进一步检测Spp001的裂解活性,我们使用扩散法和比浊法分析了在腐败希瓦氏菌噬菌体裂解周期结束时释放的噬菌体中含裂解酶的部分。结果表明,部分纯化的提取物含有内溶素,这表现为对细菌肽聚糖具有高水解活性,在15分钟内OD590值下降了0.160。这些结果将有助于进一步研究天然Spp001内溶素的纯化、Spp001宿主范围的扩展以及噬菌体编码酶的应用。