首页> 外文期刊>Journal of applied microbiology >Characterization of EstCOo8 and EstC34, intracellular esterases, from the wine-associated lactic acid bacteria Oenococcus oeni and Lactobacillus hilgardii.
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Characterization of EstCOo8 and EstC34, intracellular esterases, from the wine-associated lactic acid bacteria Oenococcus oeni and Lactobacillus hilgardii.

机译:与葡萄酒相关的乳酸菌Oenococcus oeni和hilgardii hilgardii的胞内酯酶EstCOo8和EstC34的表征。

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Aim. To clone and characterize two related intracellular esterases from Oenococcus oeni and Lactobacillus hilgardii under wine-like conditions. Methods and Results. The published genome sequences for O. oeni and Lact. hilgardii were used to identify, clone and purify putative esterase genes from these species designated EstCOo8 and EstC34, respectively. Both esterases are members of family V of lipolytic enzymes. However, EstC34 contains an SGSLG nucleophilic elbow structural motif instead of the usual GGSLG motif which is conserved in other lactic acid bacteria. Both esterases exhibited greatest specificity for C2-C4pNP-linked substrates and retained activity under wine-like conditions. EstCOo8 had an optimum temperature, pH, and ethanol concentration of 40 degrees C, 5.5 and 6% (v/v), respectively. Whereas EstC34 had an optimum temperature, pH and ethanol concentration of 50 degrees C, 5.0 and 10% (v/v), respectively. Conclusions. Both esterases were stable and retained activity under conditions that would be encountered in wine. They have the potential to reduce short-chain ethyl esters such as ethyl acetate. Significance and Impact of the Study. This study provides information that might help improve the performance of LAB during malolactic fermentation in wine in the future, either by strain selection, optimization or direct enzyme addition. copyright 2012 The Society for Applied Microbiology.
机译:目标。在酒样条件下克隆和鉴定来自Oenococcus oeni和hilgardii hilgardii的两种相关细胞内酯酶。方法和结果。 O. oeni和Lact的已公开基因组序列。 hilgardii被用于从分别命名为EstCOo8和EstC34的这些物种中鉴定,克隆和纯化假定的酯酶基因。两种酯酶都是脂解酶V家族的成员。但是,EstC34包含SGSLG亲核肘结构基序,而不是其他乳酸菌中保守的通常的GGSLG基序。两种酯酶都对C 2 -C 4 pNP连接的底物表现出最大的特异性,并在类似酒的条件下保持活性。 EstCOo8的最佳温度,pH和乙醇浓度分别为40摄氏度,5.5和6%(v / v)。 EstC34的最佳温度,pH和乙醇浓度分别为50℃,5.0和10%(v / v)。结论。在葡萄酒中遇到的条件下,两种酯酶都是稳定的并保留了活性。它们具有还原短链乙酯(例如乙酸乙酯)的潜力。研究的意义和影响。这项研究提供的信息可能会通过菌株选择,优化或直接添加酶来帮助将来在葡萄酒中苹果乳酸发酵过程中提高LAB的性能。版权所有2012应用微生物学学会。

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