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首页> 外文期刊>BMC Biotechnology >Tender coconut water an economical growth medium for the production of recombinant proteins in Escherichia coli
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Tender coconut water an economical growth medium for the production of recombinant proteins in Escherichia coli

机译:温柔的椰子水是在大肠杆菌中生产重组蛋白的经济生长培养基

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摘要

Background Escherichia coli is most widely used prokaryotic expression system for the production of recombinant proteins. Several strategies have been employed for expressing recombinant proteins in E.coli . This includes the development of novel host systems, expression vectors and cost effective media. In this study, we exploit tender coconut water (TCW) as a natural and cheaper growth medium for E.coli and Pichia pastoris. Result E.coli and P.pastoris were cultivated in TCW and the growth rate was monitored by measuring optical density at 600 nm (OD600nm), where 1.55 for E.coli and 8.7 for P.pastoris was obtained after 12 and 60 hours, respectively. However, variation in growth rate was observed among TCW when collected from different localities (0.15-2.5 at OD600nm), which is attributed to the varying chemical profile among samples. In this regard, we attempted the supplementation of TCW with different carbon and nitrogen sources to attain consistency in growth rate. Here, supplementation of TCW with 25 mM ammonium sulphate (TCW-S) was noted efficient for the normalization of inconsistency, which further increased the biomass of E.coli by 2 to 10 folds, and 1.5 to 2 fold in P.pastoris. These results indicate that nitrogen source is the major limiting factor for growth. This was supported by total nitrogen and carbon estimation where, nitrogen varies from 20 to 60 mg/100 ml while carbohydrates showed no considerable variation (2.32 to 3.96 g/100 ml). In this study, we also employed TCW as an expression media for recombinant proteins by demonstrating successful expression of maltose binding protein (MBP), MBP-TEV protease fusion and a photo switchable fluorescent protein (mEos2) using TCW and the expression level was found to be equivalent to Luria Broth (LB). Conclusion This study highlights the possible application of TCW-S as a media for cultivation of a variety of microorganisms and recombinant protein expression.
机译:背景技术大肠杆菌是生产重组蛋白最广泛使用的原核表达系统。已经采用了几种策略来在大肠杆菌中表达重组蛋白。这包括新型宿主系统,表达载体和具有成本效益的培养基的开发。在这项研究中,我们利用嫩椰子水(TCW)作为大肠杆菌和巴斯德毕赤酵母的天然且廉价的生长培养基。结果在TCW中培养大肠杆菌和巴斯德毕赤酵母,并通过测量600 nm(OD 600nm )的光密度来监测生长速度,其中大肠杆菌为1.55,巴斯德毕赤酵母为8.7分别在12和60小时后获得。然而,从不同地区(OD 600nm 处为0.15-2.5)收集到的TCW中,观察到了生长速率的变化,这归因于样品之间化学特征的变化。在这方面,我们尝试用不同的碳和氮源补充TCW,以保持生长速率的一致性。在这里,用25 mM硫酸铵(TCW-S)补充TCW被认为对不一致的标准化非常有效,这进一步使大肠杆菌的生物量增加了2到10倍,而在巴斯德毕赤酵母中增加了1.5到2倍。这些结果表明氮源是生长的主要限制因素。总氮和碳估算值支持了这一点,其中氮的变化范围为20至60 mg / 100 ml,而碳水化合物的变化不大(2.32至3.96 g / 100 ml)。在这项研究中,我们还通过证明使用TCW的麦芽糖结合蛋白(MBP),MBP-TEV蛋白酶融合体和光可切换荧光蛋白(mEos2)的成功表达,将TCW用作重组蛋白的表达介质。相当于Luria Broth(LB)。结论这项研究强调了TCW-S作为培养多种微生物和重组蛋白表达的培养基的可能应用。

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