细菌氨肽酶的产酶条件优化及应用研究

被引:0
作者
魏亚娟
机构
[1] 江南大学
关键词
氨肽酶; 枯草芽孢杆菌; 发酵条件优化; 酶学性质; 大豆分离蛋白; 酶解; 脱苦;
D O I
暂无
年度学位
2008
学位类型
硕士
导师
摘要
蛋白质水解可产生肽类物质和少量氨基酸,明显改善了其溶解性、热稳定性以及营养特性,但其水解液往往会呈现苦味,应用受到了极大的限制。氨肽酶可从氨端切除苦味肽上的疏水氨基酸,从而达到脱苦的目的。本论文主要研究了氨肽酶的产酶发酵条件、酶学性质以及其在大豆分离蛋白中的应用。 优化后的最佳发酵条件为:玉米淀粉40 g/L,豆渣30 g/L,K2HPO4 3.216 g/L,KH2PO4 0.074 g/L,MgSO4?7H2O 0.3 g/L,NaCl 1g/L,CoCl2 1mL(0.1mol/L),培养时间24h,pH值7.5,接种量8%,装液量20mL/250mL,温度40oC,转速200r/min。优化后的发酵液酶活为2685.6U/mL,比原配方发酵液酶活提高了1.71倍,在7L发酵罐上扩大培养,酶活达到1200 U/mL。 粗酶液经20%~40%乙醇分级沉淀,回收率为50.3%。研究表明,酶的半衰期为22天,最适反应温度为55℃,最适pH为8.5,温度稳定范围20~70℃,pH稳定范围在8.0~10.0左右。甘油、蛋白胨对酶活的影响不大,但在含有明胶等化合物的溶液中,酶活损失较严重; Zn2+、Ni2+对酶活有较强的抑制作用,Co2+对酶活有较强的激活作用;Pepstatin有轻微抑制,EDTA有强烈抑制作用,而Co2+可解除EDTA的抑制作用;枯草芽孢杆菌Zj016氨肽酶活性中心可能结合了两个Zn2+,每个亚基一个;米氏常数Km为0.53mmol/L,最大反应速度Vmax为19.23μmol/L/min。 应用研究表明,氨肽酶与碱性蛋白酶对大豆分离蛋白协同水解的最佳水解条件为:温度50℃、pH8.5、两酶与底物浓度比均为10000U/g、底物浓度60g/L,水解时间4h,水解度达25.0%。对碱性蛋白酶单酶与双酶的水解产物研究结果对比表明:双酶水解产物的苦味明显低于单酶水解产物,几乎不呈现苦味;两种酶解产物的分离峰峰型、分子量分布及比例有较大的差异,两酶协同水解产物的疏水值均低于单酶水解产物的;两酶协同水解产物游离氨基酸含量为1610mg/L,碱性蛋白酶单酶水解产物游离氨基酸含量为1250mg/L。
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页数:49
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[1]
Fusion of Bacillus stearothermophilus leucine aminopeptidase II with the raw-starch-binding domain of Bacillus sp strain TS-23 α-amylase generates a chimeric enzyme with enhanced thermostability and catalytic activity [J].
Hua, YW ;
Chi, MC ;
Lo, HF ;
Hsu, WH ;
Lin, LL .
JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY, 2004, 31 (06) :273-277
[2]
An Aneurinibacillus sp strain AM-1 produces a proline-specific aminopeptidase useful for collagen degradation [J].
Murai, A ;
Tsujimoto, Y ;
Matsui, H ;
Watanabe, K .
JOURNAL OF APPLIED MICROBIOLOGY, 2004, 96 (04) :810-818
[3]
Purification and characterization of recombinant Streptomyces griseus aminopeptidase [J].
Ni, SXY ;
Cossar, D ;
Man, A ;
Norek, K ;
Miller, D ;
Kearse, C ;
Tsvetnitsky, V .
PROTEIN EXPRESSION AND PURIFICATION, 2003, 30 (01) :62-68
[4]
Overexpression, purification, and characterization of the recombinant leucine aminopeptidase II of Bacillus stearothermophilus [J].
Kuo, LY ;
Hwang, GY ;
Lai, YJ ;
Yang, SL ;
Lin, LL .
CURRENT MICROBIOLOGY, 2003, 47 (01) :40-45
[5]
Crystal structure of the dinuclear zinc aminopeptidase PepV from Lactobacillus delbrueckii unravels its preference for dipeptides [J].
Jozic, D ;
Bourenkow, G ;
Bartunik, H ;
Scholze, H ;
Dive, V ;
Henrich, B ;
Huber, R ;
Bode, W ;
Maskos, K .
STRUCTURE, 2002, 10 (08) :1097-1106
[6]
Debittering of protein hydrolyzates [J].
Saha, BC ;
Hayashi, K .
BIOTECHNOLOGY ADVANCES, 2001, 19 (05) :355-370
[7]
Debittering of corn gluten hydrolysate with active carbon [J].
Suh, HJ ;
Bae, SH ;
Noh, DO .
JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, 2000, 80 (05) :614-618
[8]
Dipeptidyl aminopeptidase IV and aminopeptidase P, two proline specific enzymes from the cytoplasm of guinea-pig brain: their role in metabolism of peptides containing consecutive prolines [J].
Gilmartin, L ;
O'Cuinn, G .
NEUROSCIENCE RESEARCH, 1999, 34 (01) :1-11
[9]
Hydrolysis of alanine oligopeptides by porcine muscle alanyl aminopeptidase [J].
Flores, M ;
Aristoy, MC ;
Toldrá, F .
ZEITSCHRIFT FUR LEBENSMITTEL-UNTERSUCHUNG UND-FORSCHUNG A-FOOD RESEARCH AND TECHNOLOGY, 1999, 208 (04) :264-266
[10]
Bacterial aminopeptidases: Properties and functions [J].
Gonzales, T ;
RobertBaudouy, J .
FEMS MICROBIOLOGY REVIEWS, 1996, 18 (04) :319-344