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首页> 外文期刊>American journal of enology & viticulture >Cold-Active Acid Pectinolytic System from Psychrotolerant Bacillus: Color Extraction from Red Grape Skin
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Cold-Active Acid Pectinolytic System from Psychrotolerant Bacillus: Color Extraction from Red Grape Skin

机译:耐精神芽孢杆菌的冷活性酸性果胶分解系统:从红葡萄皮中提取颜色

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Cold-active enzymes are potentially relevant to food processing and, among them, pectinases belong to the most important enzymes in the fruit juice and wine industry. Bacillus sp. CH15 from grape berries was screened for the production of cold-active acidic pectinolytic enzymes. Taxonomic studies and 16S rDNA analysis revealed that the isolate was closely related to the Bacillus subtilis group. Maximum pectinolytic activity under acidic conditions (pH 5.0) and at low temperature (20℃) was obtained after 24 hr of incubation in medium containing citrus pectin as sole carbon source (0.305 U/mL). Polymethylgalacturonase activity was the predominant pectinase under the given assay conditions, whereas highest levels of pectate lyase activity were found at 60℃. At 5 and 10℃, the enzymatic system maintained 15 and 30% of the maximum activity, respectively. This is the first report on a pectinolytic enzyme system produced by a Bacillus strain and active at 20℃ and pH 3.6, conditions similar to those in winemaking. According to classical and CIELab color parameters of short macerations with red grape skins at low temperature, the bacterial pectinolytic system produced a rapid color extraction and the macerates exhibited better chromatic characteristics than those obtained with commercial pectinases or after natural extraction. Total anthocyanin contents of the macerates with Bacillus enzyme system and after natural extraction were significantly different, whereas relative individual pigment quantities did not show any significant difference between the two treatments. In conclusion, Bacillus sp. CH15 could be used as a microbial source of cold-active acidic pectinases in red winemaking.
机译:冷活性酶可能与食品加工有关,其中,果胶酶是果汁和葡萄酒行业中最重要的酶。芽孢杆菌筛选了葡萄浆果中的CH15以生产冷活性酸性果胶分解酶。分类学研究和16S rDNA分析表明,分离株与枯草芽孢杆菌组密切相关。在含有柑橘果胶作为唯一碳源(0.305 U / mL)的培养基中孵育24小时后,在酸性条件(pH 5.0)和低温(20℃)下获得最大的果胶分解活性。在给定的测定条件下,聚甲基半乳糖醛酸酶活性是主要的果胶酶,而在60℃时果胶酸裂解酶的活性最高。在5和10℃,酶体系分别保持最大活性的15%和30%。这是关于由芽孢杆菌属菌株产生的,在20℃和pH 3.6下有活性的果胶分解酶系统的首次报道,该条件类似于酿酒中的条件。根据在低温下用红葡萄皮进行短浸软化的经典和CIELab颜色参数,细菌果胶分解系统产生了快速的颜色提取,并且与商业化的果胶酶或自然提取后的浸出液相比,其浸出液具有更好的色度特征。芽孢杆菌酶系统浸提液和自然提取后的浸软液中总花青素含量存在显着差异,而两种处理之间相对个体色素含量未显示任何显着差异。总之,芽孢杆菌属。 CH15可用作红酒酿造中冷活性酸性果胶酶的微生物来源。

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