Hirayama Satoru, Shimizu Masashi, Tsuchiya Noriko, Furukawa Soichi, Watanabe Daisuke, Shimoi Hitoshi, Takagi Hiroshi, Ogihara Hirokazu, Morinaga Yasushi
Department of Food Bioscience and Biotechnology, College of Bioresource Sciences, Nihon University, 1866 Kameino, Fujisawa, Kanagawa 252-0880, Japan.
Department of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, 1-3-1 Kagamiyama, Higashihiroshima, Hiroshima 739-8530, Japan.
J Biosci Bioeng. 2015 May;119(5):532-7. doi: 10.1016/j.jbiosc.2014.10.007. Epub 2014 Nov 7.
We examined mixed-species biofilm formation between Lactobacillus plantarum ML11-11 and both foaming and non-foaming mutant strains of Saccharomyces cerevisiae sake yeasts. Wild-type strains showed significantly lower levels of biofilm formation compared with the non-foaming mutants. Awa1p, a protein involved in foam formation during sake brewing, is a glycosylphosphatidylinositol (GPI)-anchored protein and is associated with the cell wall of sake yeasts. The AWA1 gene of the non-foaming mutant strain Kyokai no. 701 (K701) has lost the C-terminal sequence that includes the GPI anchor signal. Mixed-species biofilm formation and co-aggregation of wild-type strain Kyokai no. 7 (K7) were significantly lower than K701 UT-1 (K701 ura3/ura3 trp1/trp1), while the levels of strain K701 UT-1 carrying the AWA1 on a plasmid were comparable to those of K7. The levels of biofilm formation and co-aggregation of the strain K701 UT-1 harboring AWA1 with a deleted GPI anchor signal were similar to those of K701 UT-1. These results clearly demonstrate that Awa1p present on the surface of sake yeast strain K7 inhibits adhesion between yeast cells and L. plantarum ML11-11, consequently impeding mixed-species biofilm formation.
我们研究了植物乳杆菌ML11-11与酿酒酵母清酒酵母的起泡和不起泡突变菌株之间的混合物种生物膜形成。与不起泡突变体相比,野生型菌株的生物膜形成水平显著较低。Awa1p是一种参与清酒酿造过程中泡沫形成的蛋白质,是一种糖基磷脂酰肌醇(GPI)锚定蛋白,与清酒酵母的细胞壁相关。不起泡突变菌株日本酿造研究所701号(K701)的AWA1基因已失去包含GPI锚定信号的C末端序列。野生型菌株日本酿造研究所7号(K7)的混合物种生物膜形成和共聚集显著低于K701 UT-1(K701 ura3/ura3 trp1/trp1),而在质粒上携带AWA1的K701 UT-1菌株的水平与K7相当。携带缺失GPI锚定信号的AWA1的K701 UT-1菌株的生物膜形成和共聚集水平与K701 UT-1相似。这些结果清楚地表明,清酒酵母菌株K7表面存在的Awa1p抑制酵母细胞与植物乳杆菌ML11-11之间的粘附,从而阻碍混合物种生物膜的形成。