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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Characterization of beta-glucan formation by Lactobacillus brevis TMW 1.2112 isolated from slimy spoiled beer
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Characterization of beta-glucan formation by Lactobacillus brevis TMW 1.2112 isolated from slimy spoiled beer

机译:乳酸杆菌TMW 1.2112β-葡聚糖形成的表征从粘性损坏的啤酒中分离

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摘要

Despite several hurdles, which hinder bacterial growth in beer, certain bacteria are still able to spoil beer. One type of spoilage is characterized by an increased viscosity and slimy texture caused by exopolysaccharide (EPS) formation of lactic acid bacteria (LAB). In this study, we characterize for the first time EPS production in a beer-spoiling strain (TMW 1.2112) of Lactobacillus brevis, a species commonly involved in beer spoilage. The strain's growth dynamics were assessed and we found an increased viscosity or ropiness in liquid or on solid media, respectively. Capsular polysaccharides (CPS) and released EPS from the cells or supernatant, respectively, were analyzed via NMR spectroscopy and methylation analysis. Both are identical beta-(1 - 3)-glucans, which are ramified with beta-glucose residues at position O2. Therefore, we assume that this EPS is mainly produced as CPS and partially released into the surrounding medium, causing viscosity of e.g. beer. CPS formation was confirmed via an agglutination test. A plasmid-located glycosyltransferase-2 was found as responsible for excess beta-glucan formation, chromosomal glucanases were proposed for its degradation. The glycosyltransferase-2 gene could also be specifically identified in beer-spoiling, slime-producing Lactobacillus rossiae and Lactobacillus parabuchneri strains, suggesting it as promising marker gene for the early detection of beta-glucan-producing Lactobacilli in breweries. (C) 2017 Elsevier B.V. All rights reserved.
机译:尽管有几个障碍,其妨碍啤酒中的细菌生长,某些细菌仍然能够破坏啤酒。一种腐败的特征在于由乳酸菌的外糖(EPS)形成引起的粘度和粘性的粘性纹理增加(实验室)。在这项研究中,我们在乳酸杆菌的啤酒淘油菌株(TMW 1.2112)中首次表征了EPS生产,该物种通常涉及啤酒腐败。评估菌株的生长动态,并分别在液体或固体介质上发现了增加的粘度或绳索。通过NMR光谱和甲基化分析分别分别分别通过NMR光谱和上清液中释放来自细胞或上清液的荚膜多糖(CPS)。两者都是相同的β-(1 - & 3)葡聚糖,其用β-葡萄糖残留物在o2的位置中掺杂。因此,我们假设该EPS主要生产为CP并部分释放到周围介质中,导致粘度。啤酒。通过凝集试验证实CPS形成。发现质粒定位的糖基转移酶-2是负责过量的β-葡聚糖形成,提出了染色体葡聚糖酶的降解。糖基转移酶-2基因也可以在啤酒 - 破坏性,生产乳酸乳酸杆菌和乳酸杆菌菌株中特别鉴定出来,这表明它是早期检测啤酒厂生产β-葡聚糖乳酸杆菌的有前途的标记基因。 (c)2017年Elsevier B.V.保留所有权利。

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