龙舌兰芽孢杆菌丙烯酰胺酶催化反应中丙烯酸的提取与定量

R. Prabha, V. Nigam
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引用次数: 0

摘要

近年来,不可再生材料的减少引起了世界各国对通过生物基方法可持续生产有机酸的重大关注。克服这一问题的一种方法是使用活性萃取剂,其中使用适当的萃取剂来回收各种有机酸和无机酸。溶剂萃取法提取丙烯酸是该技术的一个实例。本研究以龙舌兰芽孢杆菌产生的丙烯酰胺酶为原料,采用溶剂法对酰胺酶催化反应进行酸萃取,合成丙烯酸。在各种溶剂中,确定乙酸乙酯(2:1,v/v)为最合适的萃取溶剂。从20毫升的酰胺酶催化反应中回收了65毫克的原料丙烯酸。采用薄层色谱法、傅里叶变换红外光谱法、高效液相色谱法、质谱法等多种分析方法对提取的丙烯酸进行鉴定、验证和定量。提取产物中丙烯酸的m / z值为73.18,与标准丙烯酸的m / z值相近。通过高效液相色谱法,从消耗的10毫米丙烯酰胺中,几乎量化了34%的生物转化(3.4毫米)。提取的丙烯酸在未来可进一步开发为化工中间体和医药。
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Extraction and quantification of acrylic acid from acrylamidase-catalyzed reaction produced by Bacillus tequilensis
The reduction of non-renewable material has raised significant concerns for several years over the sustainable production of organic acids through bio-based methods in the world. One such way to overcome this problem is to use reactive extractants, in which appropriate extractants are employed to recover various organic and inorganic acids. The extraction of acrylic acid by solvent extraction is an illustration of this technique. The current study focuses on the synthesis of acrylic acid from acrylamidase produced by Bacillus tequilensis , succeeded by acid extraction from the amidase-catalyzed reaction by a solvent technique. Among the various solvents, ethyl acetate (2:1, v/v) was established as the most appropriate solvent for the extraction. Exactly 65 mg of raw acrylic acid was recovered from 20 ml of the amidase-catalyzed reaction. Various analytical methods such as thin layer chromatography, fourier transform infrared spectroscopy, high-performance liquid chromatography (HPLC), and mass spectrophotometry were accomplished for the identification, validation, and quantification of the extracted acrylic acid. The m / z value of acrylic acid obtained in the extracted product was 73.18, which was similar to the standard acrylic acid. From HPLC, almost 34% of bioconversion was quantified (3.4 mM) from 10 mM of acrylamide consumed. The extracted acrylic acid can be further exploited as chemical intermediates and pharmaceuticals in the future.
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