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Purification and Characterization of an Alkaline Protease from the Marine Yeast Aureobasidium pullulans for Bioactive Peptide Production from Different Sources

机译:来自海洋酵母金黄色葡萄球菌的碱性蛋白酶的纯化和表征,用于生产不同来源的生物活性肽

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The extracellular alkaline protease in the supernatant of cell culture of the marine yeast Aureobasidium pullulans 10 was purified to homogeneity with a 2.1-fold increase in specific protease activity as compared to that in the supernatant by ammoniumsulfate fractionation, gel filtration chromatog-raphy (Sephadex~(TM) G-75), and anion-exchange chromatography (DEAE Sepharose Fast Flow). According to the sodium dodecyl sulfate-polyacryl-amide gel electrophoresis data, the molecular mass of the purified enzyme was estimated to be 32.0 kDa. The optimal pH and temperature of the purified enzyme were 9.0 and 45°C, respectively. The enzyme was activated by Cu~(2+) (at a concentration of 1.0 mM) and Mn~(2+) and inhibited by Hg~(2+), Fe~(2+), Fe~(2+), Zn~(2+), and Co~(2+). The enzyme was strongly inhibited by phenylmethylsulfonyl fluoride, but weakly inhibited by EDTA, 1-10-phenanthroline, and iodoacetic acid. The K_m and V_(max) values of the purified enzyme for casein were 0.25 mg/ml and 0.0286 mu mol/min/mg of protein, respectively. After digestion of shrimp protein, spirulina (Arthospira platensis) protein, proteins of marine yeast strains N3C (Yarrowia lipolytica) and YA03a (Hanseniaspora uvaium), milk protein, and casein with the purified alkalineprotease, angiotensin I converting enzyme (ACE) inhibitory activities of the resulting peptides reached 85.3%, 12.1%, 29.8%, 22.8%, 14.1%, and 15.5%, respectively, while the antioxidant activities of these were 52.1%. 54.6%, 25.1%, 35%, 12.5%, and 24.2%,respectively, indicating that ACE inhibitory activity of the resulting peptides from the shrimp protein and antioxidant activity of those produced from the spirulina protein were the highest, respectively. These results suggest that the bioactive peptides produced by digestion of the shrimp protein with the purified alkaline protease have potential applications in the food and pharmaceutical industries.
机译:通过硫酸铵分级分离,凝胶过滤层析法(Sephadex〜),将海洋酵母金黄色葡萄球菌10细胞培养上清液中的细胞外碱性蛋白酶纯化至同质,比蛋白酶活性增加2.1倍。 (TM)G-75)和阴离子交换色谱法(DEAE Sepharose Fast Flow)。根据十二烷基硫酸钠-聚丙烯酰胺凝胶电泳数据,纯化的酶的分子量估计为32.0kDa。纯化后的酶的最佳pH和温度分别为9.0和45°C。该酶被Cu〜(2+)(浓度为1.0 mM)和Mn〜(2+)激活,并被Hg〜(2 +),Fe〜(2 +),Fe〜(2+)抑制, Zn〜(2+)和Co〜(2+)。该酶被苯甲基磺酰氟强烈抑制,但被EDTA,1-10菲咯啉和碘乙酸弱抑制。纯化的酪蛋白酶的K_m和V_(max)值分别为0.25 mg / ml和0.0286μmol/ min / mg蛋白质。消化虾蛋白,螺旋藻(Arthospira platensis)蛋白,海洋酵母菌株N3C(解脂耶氏酵母(Yarrowia lipolytica))和YA03a(Hanseniaspora uvaium)的蛋白,牛奶蛋白和酪蛋白后,纯化的碱性蛋白酶,血管紧张素I转化酶(ACE)抑制活性所得肽分别达到85.3%,12.1%,29.8%,22.8%,14.1%和15.5%,而这些肽的抗氧化活性为52.1%。分别由虾蛋白产生的肽的ACE抑制活性和由螺旋藻蛋白产生的肽的抗氧化活性分别最高,分别为54.6%,25.1%,35%,12.5%和24.2%。这些结果表明,通过用纯化的碱性蛋白酶消化虾蛋白而产生的生物活性肽在食品和制药工业中具有潜在的应用。

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