首页> 外文期刊>Journal of Agricultural and Food Chemistry >Novel Protease-Resistant Exochitinase (Echi47) from Pig Fecal Environment DNA with Application Potentials in the Food and Feed Industries
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Novel Protease-Resistant Exochitinase (Echi47) from Pig Fecal Environment DNA with Application Potentials in the Food and Feed Industries

机译:来自猪粪便环境DNA的新型耐蛋白酶蛋白酶(Echi47)及其在食品和饲料工业中的应用潜力

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摘要

A novel exochitinase gene (Echi47) was directly cloned from the pig fecal environment DNA using the genomic walking PCR technique and expressed in Escherichia coli BL21 (DE3). Echi47 has an open reading frame (ORE) of 1,161 bp encoding 386 amino acids. The amino acid sequence of Echi47 showed 36% identity with that of chitinase from Coprinellus congregatus. The recombinant exochitinase was purified with specific activity toward colloidal chitin of 6.84 U/mg. Echi47 was optimally active at pH 5.0 and 40 degrees C, respectively. When colloidal chitin was used as substrate, N-acetylthitobiose [(GlcNAc)(2)] was mostly produced at the initial stage, suggesting that it is an exochitinase. Echi47 exhibited excellent resistance to pepsin, trypsin, proteinase K, and flavor protease. Under simulated alimentary tract conditions, Echi47 was stable and active, releasing, 21.1 mg of N-acetylchitooligosactharides from 80 mg of colloidal chitin. These properties make Echi47 a potential additive in the food and feed industries.
机译:使用基因组步行PCR技术直接从猪粪便环境DNA中克隆了一个新的外切酶基因(Echi47),并在大肠杆菌BL21(DE3)中表达。 Echi47具有1,161 bp的开放阅读框(ORE),编码386个氨基酸。 Echi47的氨基酸序列与鸡腿菇壳多糖的几丁质酶具有36%的同一性。以6.84U / mg的针对胶体几丁质的比活性纯化重组的外切酶。 Echi47分别在pH 5.0和40℃下具有最佳活性。当使用胶质甲壳质作为底物时,N-乙酰硫代二糖[(GlcNAc)(2)]主要在初始阶段产生,表明这是一种外切酶。 Echi47对胃蛋白酶,胰蛋白酶,蛋白酶K和风味蛋白酶表现出优异的抗性。在模拟的消化道条件下,Echi47稳定且活跃,可从80 mg的胶质几丁质中释放21.1 mg的N-乙酰基壳寡糖。这些特性使Echi47成为食品和饲料行业的潜在添加剂。

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