Jin Q, Li L, Kim Y J, Han N S
Department of Food Science, Yanbian University, Yanji, Jilin, China.
J Appl Microbiol. 2014 Oct;117(4):1104-12. doi: 10.1111/jam.12587. Epub 2014 Jul 14.
Leuconostoc citreum is an important lactic acid bacterium in fermented foods, but dextran production often causes undesired ropiness. To prevent this side effect, a dextran-free mutant needs to be created.
Homologous recombination of the dextransucrase gene (dsrC) was conducted using a segregationally unstable plasmid, pCBM32-DSUDs. A mutant was obtained on sucrose agar medium, and a site-specific insertional inactivation in the gene was confirmed. When cultured in sucrose medium, the mutant strain produced no dextransucrase or dextran. Additionally, it showed a longer lag phase (9 h) than the wild-type strain (3 h), providing new insights into the role of dextransucrase in carbohydrate metabolism of Leuconostoc.
In this study, a dextransucrase knockout mutant was constructed. It was found that Leuc. citreum dextransucrase not only synthesizes dextran for cell protection but also provides fructose as an important carbon source for cell growth.
This knockout mutation was generated for the first time in Leuc. citreum. The dextran-free mutant has the potential to be used for various industrial purposes, including as a starter culture for production of nonviscous fermented foods and as a dextran-free host for production of recombinant proteins.
柠檬明串珠菌是发酵食品中的一种重要乳酸菌,但葡聚糖的产生常常导致不期望的黏稠现象。为防止这种副作用,需要构建一个无葡聚糖突变体。
使用一种分离不稳定质粒pCBM32-DSUDs对葡聚糖蔗糖酶基因(dsrC)进行同源重组。在蔗糖琼脂培养基上获得了一个突变体,并证实该基因发生了位点特异性插入失活。当在蔗糖培养基中培养时,突变菌株不产生葡聚糖蔗糖酶或葡聚糖。此外,它的延滞期(9小时)比野生型菌株(3小时)更长,这为葡聚糖蔗糖酶在柠檬明串珠菌碳水化合物代谢中的作用提供了新的见解。
在本研究中,构建了一个葡聚糖蔗糖酶敲除突变体。发现柠檬明串珠菌的葡聚糖蔗糖酶不仅为细胞保护合成葡聚糖,还为细胞生长提供果糖作为重要的碳源。
这种敲除突变首次在柠檬明串珠菌中产生。无葡聚糖突变体有潜力用于各种工业用途,包括作为生产非黏性发酵食品的起始培养物以及作为生产重组蛋白的无葡聚糖宿主。