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基于限制性片段长度多态性分析的泰国发酵香肠发酵及储存过程中乳酸菌种群动态

Lactic acid bacterial population dynamics during fermentation and storage of Thai fermented sausage according to restriction fragment length polymorphism analysis.

作者信息

Wanangkarn Amornrat, Liu Deng-Cheng, Swetwiwathana Adisorn, Jindaprasert Aphacha, Phraephaisarn Chirapiphat, Chumnqoen Wanwisa, Tan Fa-Jui

机构信息

Department of Agricultural Science, Naresuan University, Phitsanulok 65000, Thailand.

Department of Animal Science, National Chung Hsing University, Taichung 402, Taiwan.

出版信息

Int J Food Microbiol. 2014 Sep 1;186:61-7. doi: 10.1016/j.ijfoodmicro.2014.06.015. Epub 2014 Jun 26.

Abstract

This study applied restriction fragment length polymorphism (RFLP) analysis to identify the lactic acid bacteria (LAB) isolated from "mum" Thai fermented sausages during fermentation and storage. A total of 630 lactic acid bacteria were isolated from the sausages prepared using 2 methods. In Method 1, after stuffing, the sausages were stored at 30 °C for 14 days. In Method 2, after stuffing and storage at 30 °C for 3 days, the sausages were vacuum-packed and stored at 4 °C until Day 28. The sausages were sampled on Days 0, 3, 14, and 28 for analyses. The 16S rDNA was amplified and digested using restriction enzymes. Of the restriction enzymes evaluated, Dde I displayed the highest discrimination capacity. The LAB were classified and 7 species were identified For Methods 1 and 2, during fermentation, the Lactobacillus sakei and Lactobacillus plantarum species were dominant. For Method 2, the proportion of Leuconostoc mesenteroides markedly increased during storage, until L. sakei and Ln. mesenteroides represented the dominant species. The identification of LAB in the sausage samples could facilitate the selection of appropriate microorganisms for candidate starter cultures for future controlled mum production.

摘要

本研究应用限制性片段长度多态性(RFLP)分析来鉴定在发酵和储存过程中从泰国“mum”发酵香肠中分离出的乳酸菌(LAB)。使用两种方法制备香肠,共从中分离出630株乳酸菌。在方法1中,灌制后香肠在30℃下储存14天。在方法2中,灌制后在30℃下储存3天,然后将香肠真空包装并在4℃下储存至第28天。在第0、3、14和28天对香肠进行采样分析。使用限制性内切酶对16S rDNA进行扩增和消化。在所评估的限制性内切酶中,Dde I显示出最高的鉴别能力。对乳酸菌进行了分类并鉴定出7个种。对于方法1和方法2,在发酵过程中,清酒乳杆菌和植物乳杆菌占主导地位。对于方法2,在储存期间肠膜明串珠菌的比例显著增加,直至清酒乳杆菌和肠膜明串珠菌成为优势种。鉴定香肠样品中的乳酸菌有助于选择合适的微生物作为候选发酵剂,用于未来可控的“mum”生产。

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