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参与可可发酵的芽孢杆菌的分子鉴定和果胶裂解酶的产生。

Molecular identification and pectate lyase production by Bacillus strains involved in cocoa fermentation.

机构信息

Laboratoire de Biotechnologies, UFR Bisociences, Université Cocody/Abidjan, Abidjan, Cote d'Ivoire.

出版信息

Food Microbiol. 2011 Feb;28(1):1-8. doi: 10.1016/j.fm.2010.07.020. Epub 2010 Aug 14.

Abstract

We have previously reported the implication of Bacillus in the production of pectinolytic enzymes during cocoa fermentation. The objective of this work was to identify the Bacillus strains isolated from cocoa fermentation and study their ability to produce pectate lyase (PL) in various growth conditions. Ninety-eight strains were analyzed by Amplified Ribosomal DNA Restriction Analysis (ARDRA). Four different banding patterns were obtained leading to the clustering of the bacterial isolates into 4 distinct ARDRA groups. A subset of representative isolates for each group was identified by 16S rRNA gene partial sequencing. Six species were identified: Bacillus subtilis, Bacillus pumilus, Bacillus sphaericus, Bacillus cereus, Bacillus thuringiensis, together with Bacillus fusiformis which was isolated for the first time from cocoa fermentation. The best PL producers, yielding at least 9 U/mg of bacterial dry weight, belonged to B. fusiformis, B. subtilis, and B. pumilus species while those belonging to B. sphaericus, B. cereus and B. thuringiensis generally showed a low level of activity. Two kinds of PL were produced, as revealed by isoelectrofocusing: one with a pI of 9.8 produced by B. subtilis and B. fusiformis, the other with a pI of 10.5 was produced by B. pumilus. Strains yielded about 2 fold more PL in a pectic compound medium than in glucose medium and maximum enzyme production occurred in the late stationary bacterial growth phase. Together all these results indicate that PL production in the bacilli studied is modulated by the growth phase and by the carbon source present in the medium.

摘要

我们之前曾报道过芽孢杆菌在可可发酵过程中产生果胶酶的作用。本工作的目的是鉴定从可可发酵中分离出的芽孢杆菌菌株,并研究它们在各种生长条件下产生果胶裂解酶(PL)的能力。通过扩增核糖体 DNA 限制分析(ARDRA)分析了 98 株菌株。得到了 4 种不同的带型,导致细菌分离物聚类为 4 个不同的 ARDRA 组。每组选择有代表性的分离株进行 16S rRNA 基因部分测序鉴定。共鉴定出 6 个种:枯草芽孢杆菌、短小芽孢杆菌、球形芽孢杆菌、蜡样芽孢杆菌、苏云金芽孢杆菌,以及首次从可可发酵中分离出的梭状芽孢杆菌。PL 产量至少为 9 U/mg 细菌干重的最佳产酶菌属于梭状芽孢杆菌、枯草芽孢杆菌和短小芽孢杆菌,而属于球形芽孢杆菌、蜡样芽孢杆菌和苏云金芽孢杆菌的产酶菌通常显示出较低的活性。通过等电聚焦揭示了两种类型的 PL 的产生:枯草芽孢杆菌和梭状芽孢杆菌产生的等电点为 9.8 的 PL,短小芽孢杆菌产生的等电点为 10.5 的 PL。在果胶复合培养基中,菌株产生的 PL 比在葡萄糖培养基中多 2 倍,最大酶产量出现在细菌生长的晚期稳定期。所有这些结果表明,在所研究的芽孢杆菌中,PL 的产生受生长阶段和培养基中存在的碳源的调节。

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