Li Yahui, Ma Yanhong, Huang Kaihong, Zhang Hongzhi
Pol J Microbiol. 2016;65(2):209-13.
β-D-glucosidase (βG) gene from Oenococcus oeni SD-2a and 31MBR was cloned, sequenced and analyzed, also intracellular βG of the two strains was further localized. The results showed that βG gene of the two strains was in high homology (> 99%) to reported βG gene, confirming both strains possess βG activity at the molecular level. Intracellular βG of SD-2a is a mainly soluble protein, existing mostly in the cytoplasm and to some extent in the periplasm. While for 31MBR, intracellular βG is mainly insoluble protein existing in the cytoplasmic membrane. This study provides basic information for further study of the metabolic mechanism of βG from O. oeni SD-2a and 31MBR.
对来自酒类酒球菌SD - 2a和31MBR的β - D - 葡萄糖苷酶(βG)基因进行了克隆、测序和分析,同时对这两株菌的细胞内βG进行了进一步定位。结果表明,这两株菌的βG基因与已报道的βG基因具有高度同源性(> 99%),从分子水平证实了这两株菌均具有βG活性。SD - 2a的细胞内βG主要是可溶性蛋白,大多存在于细胞质中,在周质中也有一定程度的存在。而对于31MBR,细胞内βG主要是存在于细胞膜中的不溶性蛋白。本研究为进一步研究酒类酒球菌SD - 2a和31MBR中βG的代谢机制提供了基础信息。