Endo Akihito, Okada Sanae
Nodai Culture Collection Center, Department of Brewing, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya, Tokyo 156-8502, Japan.
J Biosci Bioeng. 2005 Mar;99(3):216-21. doi: 10.1263/jbb.99.216.
The presence of lactic acid bacteria (LAB) during shochu fermentation was monitored by PCR-denaturing gradient gel electrophoresis (DGGE) and by bacteriological culturing. No LAB were detected from fermented mashes by PCR-DGGE using a universal bacterial PCR primer set. However, PCR-DGGE using a new primer specific for the 16S rDNA of Lactococcus, Streptococcus, Tetragenococcus, Enterococcus, and Vagococcus and two primers specific for the 16S rDNA of Lactobacillus, Pediococcus, Leuconostoc, and Weissella revealed that Enterococcus faecium, Lactobacillus casei, Lactobacillus fermentum, Lactobacillus nagelii, Lactobacillus plantarum, Lactococcus lactis, Leuconostoc citreum, Leuconostoc mesenteroides, and Weissella cibaria inhabited in shochu mashes. It was also found that the LAB community composition during shochu fermentation changed after the main ingredient and water were added during the fermentation process. Therefore, we confirmed that PCR-DGGE using all three primers specific for groups of LAB together was well suited to the study of the LAB diversity in shochu mashes. The results of DGGE profiles were similar to the results of bacteriological culturing. In conclusion, LAB are present during shochu fermentation but not dominant.
通过聚合酶链反应-变性梯度凝胶电泳(PCR-DGGE)和细菌培养对烧酒发酵过程中乳酸菌(LAB)的存在情况进行了监测。使用通用细菌PCR引物对,通过PCR-DGGE未从发酵醪中检测到乳酸菌。然而,使用针对乳酸球菌、链球菌、四联球菌、肠球菌和漫游球菌16S rDNA的新引物以及针对乳酸杆菌、片球菌、明串珠菌和魏斯氏菌16S rDNA的两种引物进行PCR-DGGE分析发现,屎肠球菌、干酪乳杆菌、发酵乳杆菌、纳氏乳杆菌、植物乳杆菌、乳酸乳球菌、柠檬明串珠菌、肠膜明串珠菌和西巴魏斯氏菌存在于烧酒醪中。还发现,在发酵过程中添加主要成分和水后,烧酒发酵过程中乳酸菌群落组成发生了变化。因此,我们证实,一起使用针对乳酸菌组的所有三种引物进行PCR-DGGE分析非常适合研究烧酒醪中乳酸菌的多样性。DGGE图谱结果与细菌培养结果相似。总之,烧酒发酵过程中存在乳酸菌,但不占主导地位。