提高莱茵衣藻生长和重组Mcherry表达的培养策略。

IF 3.5 4区 生物学 Q2 MICROBIOLOGY
Jassiara da Silva Pessoa, Bruno Guzzo da Silva, Ednilson Donisete de França Júnior, Isac José da Silva Filho, João Vitor Dutra Molino, João Carlos Monteiro de Carvalho, Livia Seno Ferreira-Camargo
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引用次数: 0

摘要

莱茵衣藻是一种很有前途的重组分子生产模式微藻。然而,低产量对其工业应用是一个挑战。在实验室条件下,研究了氯化铵(NH4Cl)浓度和温度对表达mCherry荧光蛋白的转基因莱茵哈蒂球虫生长的影响。采用中心复合旋转式设计确定培养条件。NH4Cl浓度在400 ~ 647.49 mg/L之间,温度在25℃~ 32.1℃之间,细胞浓度和mCherry荧光达到最大值。较低的温度(15°C-17°C)更适合总可溶性蛋白的积累。这些结果表明,栽培条件对莱茵冷杉的生长有积极的影响,可以采用一系列的条件。与遗传方法不同,本研究提供了一种提高莱茵弧菌生长和重组蛋白表达的解决方案。这些发现为扩大莱茵梭菌作为工业生物工厂的使用铺平了道路,并可应用于其他微藻系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cultivation Strategies to Improve Chlamydomonas reinhardtii Growth and Recombinant Mcherry Expression

Chlamydomonas reinhardtii is a promising model microalga for recombinant molecules production. Nonetheless, low yield is a challenge for its industrial use. This work investigated the influence of ammonium chloride (NH4Cl) concentration and temperature on the growth of transgenic C. reinhardtii expressing the fluorescent protein mCherry on a laboratory scale. A Central Composite Rotatable Design was used to establish the cultivation conditions. NH4Cl concentrations ranging from 400 to 647.49 mg/L and temperatures between 25°C and 32.1°C resulted in maximum values of cell concentration and mCherry fluorescence. Lower temperatures (15°C–17°C) were found to be more suitable for the accumulation of total soluble proteins. These results demonstrate that cultivation conditions can positively affect C. reinhardtii growth, with a range of conditions that can be used. Unlike genetic approaches, this study provides a solution to enhance both growth and recombinant protein expression in C. reinhardtii. These findings pave the way for scaling up the use of C. reinhardtii as a biofactory in industry and can be applied to other microalgal systems.

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来源期刊
Journal of Basic Microbiology
Journal of Basic Microbiology 生物-微生物学
CiteScore
6.10
自引率
0.00%
发文量
134
审稿时长
1.8 months
期刊介绍: The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions. Papers published deal with: microbial interactions (pathogenic, mutualistic, environmental), ecology, physiology, genetics and cell biology/development, new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications) novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).
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