Suppr超能文献

利用嗜酸单宁酶合成没食子酸丙酯,同时利用海洋曲霉 BTMFW032 生产单宁酶和没食子酸。

Propyl gallate synthesis using acidophilic tannase and simultaneous production of tannase and gallic acid by marine Aspergillus awamori BTMFW032.

机构信息

Department of Biotechnology, Microbial Technology Laboratory, Cochin University of Science and Technology, Cochin, 682022, Kerala, India.

出版信息

Appl Biochem Biotechnol. 2011 Jul;164(5):612-28. doi: 10.1007/s12010-011-9162-x. Epub 2011 Jan 29.

Abstract

Marine Aspergillus awamori BTMFW032, recently reported by us, produce acidophilic tannase as extracellular enzyme. Here, we report the application of this enzyme for synthesis of propyl gallate by direct transesterification of tannic acid and in tea cream solubilisation besides the simultaneous production of gallic acid along with tannase under submerged fermentation by this fungus. This acidophilic tannase enabled synthesis of propyl gallate by direct transesterification of tannic acid using propanol as organic reaction media under low water conditions. The identity of the product was confirmed with thin layer chromatography and Fourier transform infrared spectroscopy. It was noted that 699 U/ml of enzyme could give 60% solubilisation of tea cream within 1 h. Enzyme production medium was optimized adopting Box-Behnken design for simultaneous synthesis of tannase and gallic acid. Process variables including tannic acid, sodium chloride, ferrous sulphate, dipotassium hydrogen phosphate, incubation period and agitation were recognized as the critical factors that influenced tannase and gallic acid production. The model obtained predicted 4,824.61 U/ml of tannase and 136.206 μg/ml gallic acid after 48 h of incubation, whereas optimized medium supported 5,085 U/ml tannase and 372.6 μg/ml of gallic acid production after 36 and 84 h of incubation, respectively, with a 15-fold increase in both enzyme and gallic acid production. Results indicated scope for utilization of this acidophilic tannase for transesterification of tannic acid into propyl gallate, tea cream solubilisation and simultaneous production of gallic acid along with tannase.

摘要

我们最近报道了海洋曲霉 BTMFW032 可以产生酸性单宁酶作为细胞外酶。在这里,我们报告了这种酶在浸没发酵中的应用,除了同时产生单宁酶和没食子酸外,还可以通过单宁酸和正丙醇的直接转酯化来合成没食子酸丙酯,以及在茶乳剂增溶中的应用。这种酸性单宁酶可以在低水条件下,使用正丙醇作为有机反应介质,通过单宁酸的直接转酯化合成没食子酸丙酯。通过薄层层析和傅里叶变换红外光谱确认了产物的同一性。值得注意的是,699 U/ml 的酶在 1 h 内可以使茶乳剂的 60%得到增溶。采用 Box-Behnken 设计优化了酶生产培养基,以同时合成单宁酶和没食子酸。发现包括单宁酸、氯化钠、硫酸亚铁、磷酸氢二钾、培养期和搅拌在内的过程变量是影响单宁酶和没食子酸生产的关键因素。获得的模型预测,在 48 h 的孵育后,单宁酶和没食子酸的产量分别为 4824.61 U/ml 和 136.206 μg/ml,而优化后的培养基在 36 和 84 h 的孵育后分别支持 5085 U/ml 单宁酶和 372.6 μg/ml 没食子酸的产生,酶和没食子酸的产量分别增加了 15 倍。结果表明,这种酸性单宁酶具有将单宁酸转化为没食子酸丙酯、茶乳剂增溶以及同时产生单宁酶和没食子酸的应用潜力。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验