Division of Biological Science and Technology, Yonsei University, Wonju, Gangwon 220-710, Republic of Korea.
J Food Sci. 2012 Oct;77(10):M572-8. doi: 10.1111/j.1750-3841.2012.02901.x. Epub 2012 Sep 5.
The bacterial community of Chungkookjang and raw rice-straw collected from various areas in South Korea was investigated using both culture-dependent and culture-independent methods. Pure cultures were isolated from Chungkookjang and raw rice-straw on tryptic soy agar plates with 72 to 121 colonies and identified by 16S rDNA gene sequence analysis, respectively. The traditional culture-based method and denaturing gradient gel electrophoresis analysis of PCR-amplified 16S rDNA confirmed that Pantoea agglomerans and B. subtilis were identified as predominant in the raw rice-straw and Chungkookjang, respectively, from Iljuk district of Gyeonggi province, P. ananatis and B. licheniformis were identified as predominant in the raw rice-straw and Chungkookjang from Wonju district of Gangwon province, and Microbacterium sp. and B. licheniformis were identified as predominant in the raw rice-straw and Chungkookjang from Sunchang district of Jeolla province. Other strains, such as Bacillus, Enterococcus, Pseudomonas, Rhodococcus, and uncultured bacteria were also present in raw rice-straw and Chungkookjang.
A comprehensive analysis of these microorganisms would provide a more detailed understanding of the biologically active components of Chungkookjang and help improve its quality. Polymerase chain reaction-denaturing gradient gel electrophoresis analysis can be successfully applied to a fermented food to detect unculturable or more species than the culture-dependent method. This technique is an effective and convenient culture-independent method for studying the bacterial community in Chungkookjang. In this study, the bacterial community of Chungkookjang collected from various areas in South Korea was investigated using both culture-dependent and culture-independent methods.
使用依赖培养和非依赖培养两种方法研究了来自韩国不同地区的忠清道和生稻草的细菌群落。在胰蛋白酶大豆琼脂平板上,分别从忠清道和生稻草中分离出纯培养物,通过 16S rDNA 基因序列分析进行鉴定。传统的基于培养的方法和 PCR 扩增 16S rDNA 的变性梯度凝胶电泳分析证实,在京畿道一竹区的生稻草和忠清道中,主要的细菌分别是成团泛菌和枯草芽孢杆菌;在江原道原州市的生稻草和忠清道中,主要的细菌分别是 P. ananatis 和地衣芽孢杆菌;在全罗南道顺昌郡的生稻草和忠清道中,主要的细菌分别是微杆菌和地衣芽孢杆菌。生稻草和忠清道中还存在其他菌株,如芽孢杆菌、肠球菌、假单胞菌、红球菌和未培养细菌。
对这些微生物进行全面分析可以更详细地了解忠清道中生物活性成分,并有助于提高其质量。聚合酶链反应-变性梯度凝胶电泳分析可成功应用于发酵食品,以检测比依赖培养方法更多的不可培养或更多种类的微生物。该技术是研究忠清道中细菌群落的一种有效、便捷的非依赖培养方法。在本研究中,使用依赖培养和非依赖培养两种方法研究了来自韩国不同地区的忠清道的细菌群落。