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作 者:冯颖杰[1] 宗红[1] 诸葛斌[1] 方慧英[1] 陆信曜[1] 孙进 冯倩[2] 丁凤姣
机构地区:[1]江南大学工业生物技术教育部重点实验室工业微生物研究中心,江苏无锡214122 [2]浙江正味食品有限公司浙江省调味食品制造工程技术研究中心,浙江义乌322000
出 处:《微生物学通报》2015年第11期2073-2078,共6页Microbiology China
基 金:浙江省重大科技专项计划项目(No.2012C12004-3)
摘 要:【目的】分离纯化米曲霉蛋白酶的主要组分,分析其酶学特性,并应用于酪蛋白磷酸肽(Casein phosphopeptides,CPPs)的制备。【方法】采用硫酸铵盐析、DEAE-Sepharose FF阴离子交换层析和Butyl-sepharose HP疏水层析对米曲霉蛋白酶进行分离纯化,SDS-PAGE检测分子量与纯度,MALDI-TOF-MS检测酶切位点。【结果】得到一种蛋白酶组分(命名为PE),分子量大小为58 k D左右。该酶最适反应条件为55°C,p H 8.0,酶活被Fe3+抑制,被Mn2+激活。以酪蛋白为底物时,Km=0.36 g/L,最大反应速率Vm=18.18 mg/(L·min)。蛋白酶PE对牛胰岛素B链上-Leu-Cys-、-Val-Glu-、-Tyr-Leu-和-Arg-Gly-组成的肽键有较高的切割能力,酶切位点较多。利用其水解酪蛋白,通过钡-乙醇沉淀法得到CPPs,产率为15.87%,摩尔氮磷比r(N/P)为6.17,得到的CPPs可以使钙沉淀推迟35 min。【结论】利用米曲霉蛋白酶水解酪蛋白产生CPPs,为其在功能性食品加工方面的应用提供有利的参考。[Objective] This study aimed to purify and characterize protease from Aspergillus oryzae, and to apply in casein phosphopeptides(CPPs) preparation. [Methods] Ammonium sulfate precipitation, DEAE-Sepharose FF anion exchange chromatography and Butyl-Sepharose HP hydrophobic chromatography were performed to purify the enzyme. The molecular weight and purity were determined by SDS-PAGE, and cleavage sites were detected by MALDI-TOF-MS. [Results] A protease named PE with the weight about 58 k D was obtained from Aspergillus oryzae. Protease PE shows maximal activity at p H 8.0 and 55 °C. It was inhibited by Fe3+, and activitied by Mn2+. With casein as the substrate, Km and Vm of the protease were 0.36 g/L and 18.18 mg/(L·min), respectively. Protease PE has cleavage ability in-Leu-Cys-,-Val-Glu-,-Tyr-Leu- and-Arg-Gly- residues of bovine insulin chain B, showing a wide range of residue specificity. CPPs were obtained after proteolysis of casein using PE by barium-ethanol precipitation. Yield and r(N/P) of the CPPs were 15.87% and 6.17, respectively, and delayed calcium deposit for 35 min. [Conclusion] The research provided a reference for Aspergillus oryzae protease using in the functional food industry.
关 键 词:米曲霉 蛋白酶 分离纯化 酶学性质 酶切位点 酪蛋白磷酸肽
分 类 号:TS201.2[轻工技术与工程—食品科学]
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