基于整合功能降解组学的芽孢杆菌CN2介导的角蛋白高效降解机制研究。

Yuhong Lai, Xiuyun Wu, Xianliang Zheng, Weiguang Li, Lushan Wang
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引用次数: 4

摘要

背景:角蛋白是鸡毛的主要成分,是继纤维素和几丁质之后含量第三丰富的物质。角蛋白可以转化为高价值的化合物,被认为是一种潜在的高质量蛋白质补充剂;然而,它的顽固性使其分解成为一个挑战,并且角蛋白水解蛋白酶介导的角蛋白底物降解的作用机制尚未完全阐明。芽孢杆菌CN2具有多种蛋白酶编码基因,是富含角蛋白物质环境中的优势种。为了探索羽毛角蛋白的降解模式,本研究基于功能降解组学技术,研究了菌株CN2对羽毛的降解特性。结果:芽孢杆菌CN2具有较强的羽毛角蛋白降解活性,可在24 h内有效降解天然羽毛,使重量减轻86.70%,48 h可产生195.05±6.65 U/mL角化酶,60 h可释放0.40 mg/mL可溶性蛋白。胞外蛋白酶联盟具有广泛的底物特异性,对可溶性和不溶性蛋白具有良好的生物降解性。重要的是,细胞外蛋白质组分析揭示了高效角蛋白降解系统的存在。首先,T3 γ-谷氨酰转移酶提供还原力,打破角蛋白致密的二硫键结构。然后S8B丝氨酸内肽酶首先水解角蛋白以暴露更多的裂解位点。最后,角蛋白在M4、S8C、S8A等蛋白酶的协同作用下被降解为小肽。高效液相色谱(HPLC)和氨基酸分析表明,羽毛角蛋白水解产物中含有大量的可溶性肽和必需氨基酸。结论:芽孢杆菌CN2特异性表达γ-谷氨酰基转移酶及协同分泌内肽酶和外肽酶在羽毛角蛋白降解过程中发挥重要作用。这一发现增加了我们对角状底物降解的理解,并可能启发我们设计最佳的酶鸡尾酒,以便在工业应用中更有效地探索蛋白质资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Insights into the keratin efficient degradation mechanism mediated by Bacillus sp. CN2 based on integrating functional degradomics.

Background: Keratin, the main component of chicken feather, is the third most abundant material after cellulose and chitin. Keratin can be converted into high-value compounds and is considered a potential high-quality protein supplement; However, its recalcitrance makes its breakdown a challenge, and the mechanisms of action of keratinolytic proteases-mediated keratinous substrates degradation are not yet fully elucidated. Bacillus sp. CN2, having many protease-coding genes, is a dominant species in keratin-rich materials environments. To explore the degradation patterns of feather keratin, in this study, we investigated the characteristics of feather degradation by strain CN2 based on the functional-degradomics technology.

Results: Bacillus sp. CN2 showed strong feather keratin degradation activities, which could degrade native feathers efficiently resulting in 86.70% weight loss in 24 h, along with the production of 195.05 ± 6.65 U/mL keratinases at 48 h, and the release of 0.40 mg/mL soluble proteins at 60 h. The extracellular protease consortium had wide substrate specificity and exhibited excellent biodegradability toward soluble and insoluble proteins. Importantly, analysis of the extracellular proteome revealed the presence of a highly-efficient keratin degradation system. Firstly, T3 γ-glutamyltransferase provides a reductive force to break the dense disulfide bond structure of keratin. Then S8B serine endopeptidases first hydrolyze keratin to expose more cleavage sites. Finally, keratin is degraded into small peptides under the synergistic action of proteases such as M4, S8C, and S8A. Consistent with this, high-performance liquid chromatography (HPLC) and amino acid analysis showed that the feather keratin hydrolysate contained a large number of soluble peptides and essential amino acids.

Conclusions: The specific expression of γ-glutamyltransferase and co-secretion of endopeptidase and exopeptidase by the Bacillus sp. CN2 play an important role in feather keratin degradation. This insight increases our understanding of the keratinous substrate degradation and may inspire the design of the optimal enzyme cocktails for more efficient exploration of protein resources in industrial applications.

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