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Bioconversion of Ginsenosides from Red Ginseng Extract Using Candida allociferrii JNO301 Isolated from Meju

机译:红曲参提取物中人参假丝酵母JNO301对人参皂苷的生物转化

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摘要

Red ginseng (Panax ginseng), a Korean traditional medicinal plant, contains a variety of ginsenosides as major functional components. It is necessary to remove sugar moieties from the major ginsenosides, which have a lower absorption rate into the intestine, to obtain the aglycone form. To screen for microorganisms showing bioconversion activity for ginsenosides from red ginseng, 50 yeast strains were isolated from Korean traditional meju (a starter culture made with soybean and wheat flour for the fermentation of soybean paste). Twenty strains in which a black zone formed around the colony on esculin-yeast malt agar plates were screened first, and among them 5 strains having high beta-glucosidase activity on p-nitrophenyl-beta-D-glucopyranoside as a substrate were then selected. Strain JNO301 was finally chosen as a bioconverting strain in this study on the basis of its high bioconversion activity for red ginseng extract as determined by thin-layer chromatography (TLC) analysis. The selected bioconversion strain was identified as Candida allociferrii JNO301 based on the nucleotide sequence analysis of the 18S rRNA gene. The optimum temperature and pH for the cell growth were 20 similar to 30 degrees C and pH 5 similar to 8, respectively. TLC analysis confirmed that C. allociferrii JNO301 converted ginsenoside Rb1 into Rd and then into F2, Rb2 into compound O, Rc into compound Mc1, and Rf into Rh1. Quantitative analysis using high-performance liquid chromatography showed that bioconversion of red ginseng extract resulted in an increase of 2.73, 3.32, 33.87, 16, and 5.48 fold in the concentration of Rd, F2, compound O, compound Mc1, and Rh1, respectively.
机译:红参(Panax ginseng)是韩国的传统药用植物,含有多种人参皂苷作为主要功能成分。有必要从主要人参皂苷中除去糖部分,以获得较低的糖苷配基形式,而人参皂苷在肠道中的吸收率较低。为了从红参中筛选出对人参皂苷具有生物转化活性的微生物,从韩国传统酒(用大豆和小麦粉制成的发酵剂发酵大豆糊)中分离出50种酵母菌株。首先筛选二十种菌株,其中在esculin-酵母麦芽琼脂平板上的菌落周围形成了黑色区域,然后选择了其中以对硝基苯基-β-D-吡喃葡萄糖苷为底物具有高β-葡糖苷酶活性的5个菌株。最终,通过薄层色谱法(TLC)分析确定其对红参提取物的高生物转化活性,最终将JNO301菌株选为生物转化菌株。根据18S rRNA基因的核苷酸序列分析,选定的生物转化菌株为念珠菌JNO301。细胞生长的最佳温度和pH值分别类似于20℃和30℃,pH 5类似于8。 TLC分析证实,C。allociferrii JNO301将人参皂甙Rb1转化为Rd,然后转化为F2,Rb2转化为化合物O,Rc转化为化合物Mc1,Rf转化为Rh1。使用高效液相色谱法进行的定量分析显示,人参提取物的生物转化导致Rd,F2,化合物O,化合物Mc1和Rh1的浓度分别增加2.73、3.32、33.87、16和5.48倍。

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