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食品研究与开发:2021,42(10):179-185
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亚硝酸盐还原酶高产菌株的筛选与产酶条件的研究
(1.北京工商大学化学与材料工程学院北京市植物资源研究开发重点实验室,北京 100048;2.北京工商大学北京食品营养与人类健康高精尖创新中心,北京 100048)
Screening of High-yielding Nitrite Reductase Strains and Study on Conditions of Enzyme Production
(1.Beijing Key Laboratory of Plant Resources Research and Development,College of Chemistry and Materials Engineering,Beijing Technology and Business University,Beijing 100048,China;2.Beijing Innovation Center for Food Nutrition and Human Health,Beijing Technology and Business University,Beijing 100048,China)
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投稿时间:2020-06-13    
中文摘要: 该文从泡菜中筛选到一株高产亚硝酸盐还原酶的菌种N-6,经16SrDNA序列测序鉴定为鼠李糖乳杆菌(Lactobacillus rhamnosus)。通过优化培养基中不同碳源、氮源、磷源等营养成分、培养方式、培养温度等条件,鼠李糖乳杆菌N-6的最适培养基为:2%葡萄糖、0.5%酪蛋白胨、0.2%磷酸氢二钾,37℃通气培养,通过硫酸铵分级盐析、透析、二乙基氨基乙基纤维素(diethylaminoethylcellulose,DEAE)柱层析等方法对亚硝酸还原酶进行纯化,酶活力由60.83 U/mL提高到764.49 U/mL,有效地提高了酶纯度。
Abstract:The strain N-6,which produces high levels of nitrite reductase,was screened from pickles.It was identified as Lactobacillus rhamnosus by 16SrDNA sequencing.Nutrient composition (using different carbon,nitrogen,and phosphorus sources),cultivation method,cultivation temperature,and other conditions were optimized.The optimal medium for L.rhamnosus N-6 was as follows:2% glucose,0.5% casein peptone,0.2% dipotassium hydrogen phosphate,aerobic culture at 37℃.Purification of nitrite reductase by ammonium sulfate gradient precipitations,dialysis,diethylaminoethylcellulose anion exchange chromatography,yielded an increase in enzyme activity from 60.83 U/mL to 764.49 U/mL,effectively improving the purity of nitrite reductase.
文章编号:202110028     中图分类号:    文献标志码:
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