Zhang Lili, Yu Yang, Li Xinhua, Li Xiaona, Zhang Huajiang, Zhang Zhen, Xu Yunhe
Department of Food Science and Engineering, Jinzhou Medical UniversityJinzhou, China.
Liaoning Provincial Research Center of Meat Processing and Quality ControlJinzhou, China.
Front Microbiol. 2017 Jul 25;8:1412. doi: 10.3389/fmicb.2017.01412. eCollection 2017.
In the current study, we focused on the mechanism underlying starch flocculation by the sweet potato sour liquid. The traditional microbial techniques and 16S rDNA sequencing revealed that was dominant flocculating microorganism in sour liquid. In total, 86 bacteria, 20 yeasts, and 10 molds were isolated from the sour liquid and only eight species exhibited flocculating activity. subsp. L1 strain with a high flocculating activity was isolated and identified, and the mechanism of starch flocculation was examined. subsp. L1 cells formed chain-like structures on starch granules. Consequently, these cells connected the starch granules to one another, leading to formation of large flocs. The results of various treatments of L1 cells indicated that bacterial surface proteins play a role in flocculation and L1 cells adhered to the surface of starch granules via specific surface proteins. These surface starch-binding proteins were extracted using the guanidine hydrochloride method; 10 proteins were identified by mass spectrometry: three of these proteins were glycolytic enzymes; two were identified as the translation elongation factor Tu; one was a cell wall hydrolase; one was a surface antigen; one was lyzozyme M1; one was a glycoside hydrolase; and one was an uncharacterized proteins. This study will paves the way for future industrial application of the L1 isolate in starch processing and food manufacturing.
在本研究中,我们聚焦于甘薯酸浆使淀粉絮凝的潜在机制。传统微生物技术和16S rDNA测序表明,[具体微生物名称]是酸浆中的主要絮凝微生物。从酸浆中总共分离出86种细菌、20种酵母和10种霉菌,只有8种[具体微生物名称]表现出絮凝活性。分离并鉴定出具有高絮凝活性的[具体微生物名称]亚种L1菌株,并对淀粉絮凝机制进行了研究。[具体微生物名称]亚种L1细胞在淀粉颗粒上形成链状结构。因此,这些细胞将淀粉颗粒彼此连接起来,导致形成大的絮凝物。对L1细胞进行的各种处理结果表明,细菌表面蛋白在絮凝过程中起作用,并且L1细胞通过特定表面蛋白附着在淀粉颗粒表面。使用盐酸胍法提取这些表面淀粉结合蛋白;通过质谱鉴定出10种蛋白:其中3种蛋白是糖酵解酶;2种被鉴定为翻译延伸因子Tu;1种是细胞壁水解酶;1种是表面抗原;1种是溶菌酶M1;1种是糖苷水解酶;还有1种是未鉴定的蛋白。本研究将为L1分离株未来在淀粉加工和食品制造中的工业应用铺平道路。