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通过PCR-DGGE、SDS-PAGE和MALDI-TOF MS鉴定发酵剂拉鲁中的乳酸菌和真菌。

Identification of LAB and Fungi in Laru, a Fermentation Starter, by PCR-DGGE, SDS-PAGE, and MALDI-TOF MS.

作者信息

Ahmadsah Lenny S F, Kim Eiseul, Jung Youn-Sik, Kim Hae-Yeong

机构信息

Department of Food Science and Biotechnology & Institute of Life Sciences and Resources, Kyung Hee University, Yongin 17104, Republic of Korea.

出版信息

J Microbiol Biotechnol. 2018 Jan 28;28(1):32-39. doi: 10.4014/jmb.1705.05044.

DOI:10.4014/jmb.1705.05044
PMID:29081085
Abstract

Samples of (a fermentation starter) obtained from the upper part of Borneo Island were analyzed for their lactic acid bacteria (LAB) and fungal diversity using both a culture-independent method (PCR-DGGE) and culture-dependent methods (SDS-PAGE and MALDI-TOF MS). and were detected by all three methods. In addition, , and were detected by PCR-DGGE. In contrast, , and were detected only by the culture-dependent methods. Our results indicate that the culture-independent method can be used to determine whether multiple laru samples originated from the same manufacturing region; however, using the culture-independent and the two culture-dependent approaches in combination provides a more comprehensive overview of the laru microbiota.

摘要

从婆罗洲岛上部获取的(一种发酵剂)样本,使用非培养方法(PCR-DGGE)和培养方法(SDS-PAGE和MALDI-TOF MS)分析其乳酸菌(LAB)和真菌多样性。所有三种方法都检测到了 和 。此外,PCR-DGGE检测到了 、 和 。相比之下,只有培养方法检测到了 、 和 。我们的结果表明,非培养方法可用于确定多个laru样本是否源自同一生产区域;然而,将非培养方法与两种培养方法结合使用能更全面地了解laru微生物群。

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