Yasutake Tetsuya, Kumagai Takanori, Inoue Atsushi, Kobayashi Koei, Noda Masafumi, Orikawa Asumi, Matoba Yasuyuki, Sugiyama Masanori
Department of Molecular Microbiology and Biotechnology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Kasumi 1-2-3, Minami-ku, Hiroshima 734-8551, Japan.
Bioscience laboratories, Meiji Seika Pharma Co., Ltd, 788 Kayama, Odawara-shi, Kanagawa-ken 250-0852, Japan.
Biochem Biophys Rep. 2016 Jan 8;5:266-271. doi: 10.1016/j.bbrep.2016.01.004. eCollection 2016 Mar.
We have previously isolated a lactic acid bacterium (LAB), LP28, from the longan fruit . Since the plant-derived LAB strain produces an extracellular polysaccharide (EPS), in this study, we analyzed the chemical structure and the biosynthesizing genes for the EPS. The EPS, which was purified from the LP28 culture broth, was classified into acidic and neutral EPSs with a molecular mass of about 50 kDa and 40 kDa, respectively. The acidic EPS consisted of glucose, galactose, mannose, and -acetylglucosamine moieties. Interestingly, since pyruvate residue was detected in the hydrolyzed acidic EPS, one of the four sugars may be modified with pyruvate. On the other hand, the neutral EPS consisted of glucose, mannose, and -acetylglucosamine; pyruvate was scarcely detected in the polysaccharide molecule. As a first step to deduce the probiotic function of the EPS together with the biosynthesis, we determined the whole genome sequence of the LP28 strain, demonstrating that the genome is a circular DNA, which is composed of 1,774,865 bp (1683 ORFs) with a GC content of 37.1%. We also found that the LP28 strain harbors a plasmid carrying 6 ORFs composed of 5366 bp with a GC content of 36.5%. By comparing all of the genome sequences among the LP28 strain and four strains of reported previously, we found that 53 proteins in the LP28 strain display a similarity of less than 50% with those in the four strains. Significantly, 4 of the 53 proteins, which may be enzymes necessary for the EPS production on the LP28 strain, were absent in the other four strains and displayed less than 50% similarity with other LAB species. The EPS-biosynthetic gene cluster detected only in the LP28 genome consisted of 12 ORFs containing a priming enzyme, five glycosyltransferases, and a putative polysaccharide pyruvyltransferase.
我们之前从龙眼果实中分离出了一株乳酸菌(LAB),LP28。由于该植物源LAB菌株能产生一种胞外多糖(EPS),因此在本研究中,我们分析了EPS的化学结构和生物合成基因。从LP28培养液中纯化得到的EPS可分为酸性EPS和中性EPS,分子量分别约为50 kDa和40 kDa。酸性EPS由葡萄糖、半乳糖、甘露糖和N - 乙酰葡糖胺部分组成。有趣的是,由于在水解后的酸性EPS中检测到了丙酮酸残基,四种糖中的一种可能被丙酮酸修饰。另一方面,中性EPS由葡萄糖、甘露糖和N - 乙酰葡糖胺组成;在多糖分子中几乎检测不到丙酮酸。作为推断EPS的益生菌功能及其生物合成的第一步,我们测定了LP28菌株的全基因组序列,结果表明该基因组是一个环状DNA,由1,774,865 bp(1683个开放阅读框)组成,GC含量为37.1%。我们还发现LP28菌株含有一个携带6个开放阅读框的质粒,该质粒由5366 bp组成,GC含量为36.5%。通过比较LP28菌株与之前报道的四个菌株的所有基因组序列,我们发现LP28菌株中有53种蛋白质与这四个菌株中的蛋白质相似度低于50%。值得注意的是,这53种蛋白质中的4种可能是LP28菌株产生EPS所需的酶,在其他四个菌株中不存在,并且与其他LAB物种的相似度低于50%。仅在LP28基因组中检测到的EPS生物合成基因簇由12个开放阅读框组成,包括一个引发酶、五个糖基转移酶和一个假定的多糖丙酮酸转移酶。