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Acidic Chitinase-Chitin Complex Is Dissociated in a Competitive Manner by Acetic Acid: Purification of Natural Enzyme for Supplementation Purposes

机译:通过乙酸以竞争方式解离酸性丁蛋白酶--Chitin复合物:纯化天然酶以补充目的

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摘要

Acidic chitinase (Chia) has been implicated in asthma, allergic inflammations, and food processing. We have purified Chia enzymes with striking acid stability and protease resistance from chicken and pig stomach tissues using a chitin column and 8 M urea (urea-Chia). Here, we report that acetic acid is a suitable agent for native Chia purification from the stomach tissues using a chitin column (acetic acid-Chia). Chia protein can be eluted from a chitin column using 0.1 M acetic acid (pH 2.8), but not by using Gly-HCl (pH 2.5) or sodium acetate (pH 4.0 or 5.5). The melting temperatures of Chia are not affected substantially in the elution buffers, as assessed by differential scanning fluorimetry. Interestingly, acetic acid appears to be more effective for Chia-chitin dissociation than do other organic acids with similar structures. We propose a novel concept of this dissociation based on competitive interaction between chitin and acetic acid rather than on acid denaturation. Acetic acid-Chia also showed similar chitinolytic activity to urea-Chia, indicating that Chia is extremely stable against acid, proteases, and denaturing agents. Both acetic acid- and urea-Chia seem to have good potential for supplementation or compensatory purposes in agriculture or even biomedicine.
机译:酸性丁蛋白酶(Chia)涉及哮喘,过敏性炎症和食品加工。我们使用一丁蛋白柱和8米尿素(脲壳),纯化的Chia酶具有醒目的酸稳定性,蛋白酸稳定性和蛋白酶耐药性,患有鸡肉和猪胃组织。在这里,我们报告说,乙酸是使用几丁蛋白柱(乙酸 - Chia)从胃组织纯化的合适剂。可以使用0.1m乙酸(pH2.8)从几丁质柱洗脱Chia蛋白,但不是使用甘氨酸 - HCl(pH2.5)或乙酸钠(pH 4.0或5.5)。如通过差示扫描荧光测定法评估的洗脱缓冲液中,Chia的熔化温度不会受到洗脱缓冲液的影响。有趣的是,乙酸似乎对Chia-Chitin解离比与具有相似结构的其他有机酸更有效。我们提出基于几丁质和乙酸之间的竞争性相互作用而不是酸性变性的新解离的新概念。醋酸 - Chia还显示出与尿素Chia相似的依托碱性活性,表明Chia对酸,蛋白酶和变性剂非常稳定。醋酸和尿素似乎似乎具有良好的农业甚至生物医学中的补充或补偿目的的潜力。

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