鞘氨醇单胞菌的3-苯氧基苯甲酸降解酶定位及分子质量确定  被引量:2

Positioning and determined molecular weight of 3-phenoxyzoic acid degrading-enzyme by Sphingomonas sp.

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作  者:李建龙[1] 王志龙[1] 刘书亮[1] 姚开[2] 邓维琴 黄道梅 赖海梅 

机构地区:[1]四川农业大学食品学院,四川雅安625014 [2]四川大学轻纺与食品学院,四川成都610065

出  处:《食品与发酵工业》2014年第1期24-29,共6页Food and Fermentation Industries

基  金:国家自然科学基金面上资助项目(31371775)

摘  要:对鞘氨醇单胞菌(Sphingomonas sp.)SC-1产3-苯氧基苯甲酸(3-PBA)降解酶的细胞定位分析,得出该降解酶主要位于细胞碎片上;用蔗糖密度梯度离心法分离浓缩细胞碎片中的细胞膜片段并检测其对3-PBA的降解,结果表明细胞膜片段具有定的3-PBA降解酶活性,推测该酶是类位于细胞膜上的膜蛋白;Native-PAGE分离细胞膜样品中的膜蛋白并切胶回收作对3-PBA的降解反应,条带c对3-PBA有定的降解活性,对条带c进行SDS-PAGE分析,推断出该降解酶的分子质量约为50~90 ku。The cell localization analysis of 3- Phenoxybenzoic acid degrading-enzyme produced by Sphingomonas sp.SC-1 was studied in this article.The analysis showed that the degrading-enzyme was mainly located in the cell fragments.Separating the cell membrane fragments from concentration cell fragments by using sucrose density gradient centrifugation and detecting the effect on degrading 3-PBA.The result shows that the membrane fragments have some certain 3- phenoxybenzoic acid-degrading activity and it can be speculated that this enzyme is one kind of membrane protein on the cell membrane.Membrane protein with gel extraction separated from the sample by Native-PAGE was used to degrade 3- phenoxybenzoic acid.The band"c "had certain degrading activity.Using SDS-PAGE to analyze the band "c "and figure out that the molecular mass of degrading-enzyme is about 50 ~ 90 ku.

关 键 词:3-苯氧基苯甲酸降解酶 定位 分子质量 鞘氨醇单胞菌 

分 类 号:TS201.2[轻工技术与工程—食品科学]

 

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