Xiong Jing-Jing, Ren Jia-Xiu, Zhou Shu-Han, Su Ming-Sheng, Wang Li-Yuan, Weng Mei-Zhi, Xie Wei-Hua, Xie Xiao-Mei
Key Laboratory of Modern Preparation of Traditional Chinese Medicine, Ministry of Education, Jiangxi University of Traditional Chinese Medicine Nanchang 330004, China.
Chaohu Hospital Affiliated to Anhui Medical University Hefei 238000, China.
Zhongguo Zhong Yao Za Zhi. 2019 Jun;44(11):2266-2273. doi: 10.19540/j.cnki.cjcmm.20190321.301.
A high-content GABA was found in Sojae Semen Praeparatum(SSP), which is a famous traditional Chinese medicine and officially listed in Chinese Pharmacopoeia. To screen out and identify GABA-producing microbes from samples at different time points during the fermenting process of SSP, traditional microbiological methods combined with molecular biological methods were used to study the predominant GABA-producing microorganisms existing in the fermenting process of SSP. This study would lay a foundation for further studying the processing mechanism of SSP. The fermenting process of SSP was based on Chinese Pharmacopoeia(2010 edition), and samples were taken at different time points during the fermenting process of SSP. The bacteria and fungi from samples at different time points in the fermenting process of SSP were cultured, isolated and purified by selective medium, and dominant strains were selected. The dominant bacteria were cultured in the designated liquid medium to prepare the fermentation broths, and GABA in the fermentation broth was qualitatively screened out by thin-layer chromatography. The microbial fermentation broth with GABA spots in the primary screening was quantitatively detected by online pre-column derivatization and high performance liquid chromatography established in our laboratory. GABA-producing microorganisms were screened out from predominant strains, and their GABA contents in fermentation broth were determined. The DNA sequences of GABA-producing bacteria and fungi were amplified using 16S rDNA and 18S rDNA sequences by PCR respectively. The amplified products were sequenced, and the sequencing results were identified through NCBI homology comparison. Molecular biological identification was made by phylogenetic tree constructed by MEGA 7.0 software. Through the homology comparison of NCBI and the construction of phylogenetic tree by MEGA 7.0 software, nine GABA-producing microorganisms were screened out and identified in this study. They were Bacillus subtilis, Enterococcus faecium, E. avium, Aspergillus tamarii, A. flavus, A. niger, Cladosporium tenuissimum, Penicillium citrinum and Phanerochaete sordida respectively. For the first time, nine GABA-producing microorganisms were screened out and identified in the samples at different time points during the fermenting process of SSP in this study. The results indicated that multiple predominant GABA-producing microorganisms exist in the fermenting process of SSP and may play an important role in the formation of GABA.
在中药名品、被正式列入《中国药典》的淡豆豉中发现了高含量的γ-氨基丁酸(GABA)。为了从淡豆豉发酵过程中不同时间点的样品中筛选并鉴定出产生GABA的微生物,采用传统微生物学方法与分子生物学方法相结合,对淡豆豉发酵过程中存在的主要产GABA微生物进行研究。本研究将为进一步探究淡豆豉的炮制机理奠定基础。淡豆豉的发酵过程依据《中国药典》(2010年版)进行,在淡豆豉发酵过程中的不同时间点取样。采用选择性培养基对淡豆豉发酵过程中不同时间点样品中的细菌和真菌进行培养、分离和纯化,并筛选出优势菌株。将优势细菌在指定液体培养基中培养以制备发酵液,通过薄层色谱法定性筛选出发酵液中的GABA。对初筛出的带有GABA斑点的微生物发酵液,采用本实验室建立的在线柱前衍生化高效液相色谱法进行定量检测。从优势菌株中筛选出产GABA的微生物,并测定其发酵液中的GABA含量。分别采用PCR方法,利用16S rDNA和18S rDNA序列扩增产GABA细菌和真菌的DNA序列。对扩增产物进行测序,并通过NCBI同源性比对鉴定测序结果。利用MEGA 7.0软件构建系统发育树进行分子生物学鉴定。通过NCBI同源性比对及MEGA 7.0软件构建系统发育树,本研究筛选并鉴定出9株产GABA的微生物。它们分别是枯草芽孢杆菌、屎肠球菌、鸟肠球菌、酱油曲霉、黄曲霉、黑曲霉、细极链格孢、桔青霉和污色多孔菌。本研究首次在淡豆豉发酵过程中不同时间点的样品中筛选并鉴定出9株产GABA的微生物。结果表明,淡豆豉发酵过程中存在多种主要产GABA的微生物,它们可能在GABA的形成过程中发挥重要作用。