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作 者:凌海秋[1] 金湘[1] 毛培宏[1] 吕杰[1,2] 武宝山[1]
机构地区:[1]新疆大学物理科学与技术学院离子束生物技术中心,新疆乌鲁木齐830008 [2]南京工业大学制药工程与生命科学学院,江苏南京210009
出 处:《生物技术》2010年第4期64-66,共3页Biotechnology
基 金:国家自然科学基金项目(30760009);新疆大学校院联合资助项目(XY080107)资助
摘 要:目的:探讨12株重组酵母菌生物合成麻黄碱的特性及L-Phe对麻黄碱生物合成的影响。方法:以葡萄糖为碳源、NaNO3为氮源对重组酵母菌进行培养,在相同条件下,在液体培养基中添加5mg/L的L-Phe,利用反向高压液相色谱(RP-HPLC)测定重组酵母菌培养液中麻黄碱和伪麻黄碱的含量。结果:重组酵母菌培养液中麻黄碱和伪麻黄碱的最高产量分别为18.85mg/L和4.11mg/L;L-Phe对各重组菌株生物合成麻黄碱的调控作用各不相同。结论:通过L-Phe对重组酵母菌生物合成麻黄碱和伪麻黄碱调控作用的探讨,将为研究重组菌株的遗传多样性提供依据。Objective:Investigation on the characteristics of ephedrine and pseudoephedrine biosynthesis in 12 recombined yeast strains and the effects of L-phenylalanine in alkaloids biosynthesis.Method:Used of glucose as the carbon source,NaNO3 as the nitrogen source to carry on culture to the recombined yeasts,otherwise added the L-Phe of 5mgs/L under the same culture condition.The l-ephedrine and d-pseudoephedrine in the culture liquid of the recombined yeasts were analyzed by the RP-HPLC.Result:After culturing in liquid medium for 72h,extracellular l-ephedrine and d-pseudoephedrine concentrations of 18.85 mg/L and 4.11mg/L,respectively.The addition of the L-Phe to culture medium substantially changed the amount of l-ephedrine and/or d-pseudoephedrine produced by the recombined yeasts.Conclusion:The results of the regulation on L-Phe to the l-ephedrine and d-pseudoephedrine biosynthesis in recombined yeasts would be valuable for further investigations of genetical diversity.
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