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首页> 外文期刊>Journal of Biotechnology >Overexpression of a modified protein from amaranth seed in Escherichia coli and effect of environmental conditions on the protein expression.
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Overexpression of a modified protein from amaranth seed in Escherichia coli and effect of environmental conditions on the protein expression.

机译:i菜种子中修饰蛋白质在大肠杆菌中的过表达以及环境条件对蛋白质表达的影响。

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Amaranth seeds are considered as an excellent complementary source of food protein due to their balanced amino acid composition. Amarantin acidic subunit has the potential as a functional and nutraceutical protein, and it is structurally a good candidate for modification. The aim of this work was to improve its functionality, then the primary structure was modified into the third variable region of 11S globulins, by inserting antihypertensive peptides: four Val-Tyr in tandem and Arg-Ile-Pro-Pro in the C-terminal region. Modified protein was expressed in Escherichia coli Origami (DE3) and was purified. The culture conditions, including the culture media, temperature, agitation speed and air flow were tested in order to obtain an increased expression levels of the modified protein. A 23 factorial design was used for evaluate the effect of environmental conditions on modified protein production. The results indicated that the yield of modified protein could be increased by up 3-fold in bioreactor as compared with flask. In addition, the temperature, the agitation speed and the oxygen were significant factors on the expression of the antihypertensive protein. The maximum production was 99 mg protein-L--1. The hydrolyzed protein showed a high inhibitory activity of the angiotensin converting enzyme (IC50 = 0.047 mg mL--1). All rights reserved, Elsevier.
机译:由于菜的氨基酸组成均衡,因此被认为是食物蛋白质的极佳补充来源。阿玛兰汀酸性亚基具有作为功能性和营养保健蛋白的潜力,并且在结构上是修饰的良好候选者。这项工作的目的是改善其功能,然后通过插入降压肽将一级结构修饰为11S球蛋白的第三个可变区:串联的四个Val-Tyr和C末端的Arg-Ile-Pro-Pro地区。修饰的蛋白在大肠杆菌折纸(DE3)中表达并纯化。测试了培养条件,包括培养基,温度,搅拌速度和空气流量,以提高修饰蛋白的表达水平。 2 3 析因设计用于评估环境条件对修饰蛋白质生产的影响。结果表明,与烧瓶相比,在生物反应器中修饰蛋白的产量可以提高3倍。另外,温度,搅拌速度和氧气是影响降压蛋白表达的重要因素。最大产量为99 mg L-s -1 。水解蛋白对血管紧张素转化酶具有很高的抑制活性(IC 50 = 0.047 mg mL -1 )。保留所有权利,Elsevier。

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