目的采用短刺小克银汉霉AS 3.970(C.blakesleana AS 3.970)对白鲜碱展开微生物转化研究。方法利用30株丝状真菌对白鲜碱进行微生物转化,筛选出转化效果好的菌株;然后在该菌株微生物转化试验中考察接种量、转化温度、培养基pH值、转化时...目的采用短刺小克银汉霉AS 3.970(C.blakesleana AS 3.970)对白鲜碱展开微生物转化研究。方法利用30株丝状真菌对白鲜碱进行微生物转化,筛选出转化效果好的菌株;然后在该菌株微生物转化试验中考察接种量、转化温度、培养基pH值、转化时间等不同因素对白鲜碱微生物转化作用的影响,选择出最优的转化条件;在最优转化条件下,规模制备白鲜碱的微生物转化产物并进行结构鉴定。结果短刺小克银汉霉AS 3.970对白鲜碱的微生物转化效果好,在微生物转化研究中发现白鲜碱转化的最优条件是转化温度为28℃,培养基初始pH值为7.0,最适接种量5%(体积分数),转化时间为7 d;通过分离纯化和结构鉴定,最终得到两个主要转化产物,分别是4-甲氧基-2,3-二氢呋喃喹啉与3-(2-羟乙基)-4-甲氧基喹啉酮。结论通过微生物转化技术可以对白鲜碱进行微生物结构修饰。展开更多
目的对川丁特罗进行微生物转化研究。方法利用短刺小克银汉霉Cunninghamella.blakesleana AS 3.970对川丁特罗进行微生物转化,通过柱层析、液相色谱-质谱及核磁技术对川丁特罗微生物转化产物进行分离与鉴定。结果短刺小克银汉霉Cunningh...目的对川丁特罗进行微生物转化研究。方法利用短刺小克银汉霉Cunninghamella.blakesleana AS 3.970对川丁特罗进行微生物转化,通过柱层析、液相色谱-质谱及核磁技术对川丁特罗微生物转化产物进行分离与鉴定。结果短刺小克银汉霉Cunninghamella.blakesleana AS 3.970转化川丁特罗累计获得三个转化产物,分别是川丁特罗芳香羟胺代谢物、川丁特罗叔丁基羟基取代代谢物和1-羧基川丁特罗。结论通过微生物转化技术可以对川丁特罗进行微生物结构修饰。展开更多
The microbial transformation of glycyrrhetinic acid（1） by Cunninghamella blakesleana CGMCC 3.970 led to the production of five new metabolites（2-6）.The structures of the metabolites were determined by extensive sp...The microbial transformation of glycyrrhetinic acid（1） by Cunninghamella blakesleana CGMCC 3.970 led to the production of five new metabolites（2-6）.The structures of the metabolites were determined by extensive spectroscopic（HR-ESIMS,1D and 2D NMR） data analyses.The involved reactions exhibited specific hydroxylations at C-24,C-7,and C-15,and oxidation at C-3.Moreover,compounds 2,5,and 6showed significant neural anti-inflammatory activity by inhibiting lipopolysaccharide-induced NO production in mouse microglia BV2 cells with IC（50） values of 0.76,0.94,and 0.16μmol/L,respectively.展开更多
文摘目的对川丁特罗进行微生物转化研究。方法利用短刺小克银汉霉Cunninghamella.blakesleana AS 3.970对川丁特罗进行微生物转化,通过柱层析、液相色谱-质谱及核磁技术对川丁特罗微生物转化产物进行分离与鉴定。结果短刺小克银汉霉Cunninghamella.blakesleana AS 3.970转化川丁特罗累计获得三个转化产物,分别是川丁特罗芳香羟胺代谢物、川丁特罗叔丁基羟基取代代谢物和1-羧基川丁特罗。结论通过微生物转化技术可以对川丁特罗进行微生物结构修饰。
文摘The microbial transformation of glycyrrhetinic acid（1） by Cunninghamella blakesleana CGMCC 3.970 led to the production of five new metabolites（2-6）.The structures of the metabolites were determined by extensive spectroscopic（HR-ESIMS,1D and 2D NMR） data analyses.The involved reactions exhibited specific hydroxylations at C-24,C-7,and C-15,and oxidation at C-3.Moreover,compounds 2,5,and 6showed significant neural anti-inflammatory activity by inhibiting lipopolysaccharide-induced NO production in mouse microglia BV2 cells with IC（50） values of 0.76,0.94,and 0.16μmol/L,respectively.
