Enzyme substrates

  • 文章类型: Review
    β-葡糖苷酶水解糖苷键以通过催化机理从糖苷和寡糖释放非还原性末端葡糖基残基。众所周知,β-葡萄糖苷酶在生物精炼厂中用于纤维素降解,其中β-葡糖苷酶是从纤维二糖最终产生葡萄糖的限速酶。β-葡萄糖苷酶在其他工业部门用作催化剂,包括药品,啤酒厂,乳制品,和食品加工。在β-葡萄糖苷酶的帮助下,生氰苷和植物苷被转化为糖部分和苷元。这些糖苷配基化合物在食品加工和酿造工业中用作芳族化合物。根据其药理特性,它们也被用作药物和膳食补充剂。本文综述了糖苷配基的应用以及β-葡萄糖苷酶的微生物来源在糖苷配基生产中的应用。
    β-glucosidases hydrolyse glycosidic bonds to release non-reducing terminal glucosyl residues from glycosides and oligosaccharides via catalytic mechanisms. It is very well known that the β-glucosidase enzyme is used in biorefineries for cellulose degradation, where β-glucosidases is the rate-limiting enzyme for the final glucose production from cellobiose. The β-glucosidase enzyme is used as a catalyst in other industrial sectors, including pharmaceuticals, breweries, dairy, and food processing. With the aid of β-glucosidase enzymes, cyanogenic glycosides and plant glycosides are transformed into sugar moiety and aglycones. These aglycone compounds are employed as aromatic compounds in the food processing and brewing industries. They are also used as medications and dietary supplements based on their pharmacological qualities. Applications of aglycones and the microbiological sources of β-glucosidase in aglycone production have been discussed in this review.
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  • 文章类型: Journal Article
    检测能力,识别和量化细菌在临床诊断中至关重要,环境试验,食品安全环境和微生物学研究。最近,多重耐药细菌病原体的威胁推动全球科学界快速发展,可靠,具体的和负担得起的方法来检测细菌种类。使用合成修饰的酶底物是一种方便的方法来检测特定的细菌,经济和快速的方式。该方法基于对给定的细菌标记酶使用特定的酶底物,与信号生成部分缀合。酶促反应后,signalophor从合成底物中释放出来,产生特定和可测量的信号。已经描述了几种类型的信号器,并由它们产生的信号类型来定义。如显色,荧光,发光,生电和氧化还原。根据它们在水中的溶解度,信号细胞被进一步细分为几组,这是定义它们在细菌培养的固体或液体培养基上的应用的关键。这篇综合综述介绍了合成酶底物及其在细菌检测中的应用,显示了它们的作用机理和合成途径。
    The ability to detect, identify and quantify bacteria is crucial in clinical diagnostics, environmental testing, food security settings and in microbiology research. Recently, the threat of multidrug-resistant bacterial pathogens pushed the global scientific community to develop fast, reliable, specific and affordable methods to detect bacterial species. The use of synthetically modified enzyme substrates is a convenient approach to detect bacteria in a specific, economic and rapid manner. The method is based on the use of specific enzyme substrates for a given bacterial marker enzyme, conjugated to a signalogenic moiety. Following enzymatic reaction, the signalophor is released from the synthetic substrate, generating a specific and measurable signal. Several types of signalophors have been described and are defined by the type of signal they generate, such as chromogenic, fluorogenic, luminogenic, electrogenic and redox. Signalophors are further subdivided into groups based on their solubility in water, which is key in defining their application on solid or liquid media for bacterial culturing. This comprehensive review describes synthetic enzyme substrates and their applications for bacterial detection, showing their mechanism of action and their synthetic routes.
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