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作 者:应汉杰[1] 荣绍丰[1] 吕浩[1] 欧阳平凯[1]
机构地区:[1]南京化工大学生物工程与科学系
出 处:《南京化工学院学报》1998年第1期60-63,共4页
摘 要:黑曲霉(Aspergilus.niger)柠檬酸发酵培养基中添加0.08~0.15mg/L的MgCl2,对菌体浓度没显著性影响,但可使柠檬酸产率提高4%~7%,发酵旺盛期(30h)断氧30min的实验结果与正常发酵结果对照表明:添加0.1mg/LMgCl2的摇瓶产酸率下降16.2%;空白对照摇瓶产酸率则下降56.8%,通过对柠檬酸合成酶[EC4.1.3.7]酶活测定及活体染色计数,我们认为,断氧条件下,0.1mg/LMgCl2使黑曲霉存活率升高是造成上述差异的主要原因。0.08-0.15 mg/L MgCl_2 in culture medium could increase the yield of citric acid by Asp. niger up to 4%-7%, but there was not remarkably effect on mycelium concentration. The experiments broken oxygen 30 minutes were done in fermentation peak period (30 h), The results in contrast to unbroken oxygen experiments indicated that the yield of citric acid in 0.1 mg/L MgCl_2 shaking flasks decreased by 16.2%; but in the same condition the yield of citric acid in blank shaking flasks was decreased by 56.8%. Through the determination of activity of citratesynthase [EC 4.1.3.7] and vivimycelium dyeing count, We thought it was important that 0.1 mg/L MgCl_2increased the vitality ratio of Asp. niger in broken oxygen.
分 类 号:TQ921.1[轻工技术与工程—发酵工程]
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