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构建高水平 cAMP 的工业面包酵母。

Construction of industrial baker's yeast with high level of cAMP.

机构信息

Key Laboratory of Industrial Fermentation Microbiology, Ministry of Education, Tianjin Industrial Microbiology Key Laboratory, College of Biotechnology, Tianjin University of Science and Technology, Tianjin, P. R. China.

出版信息

J Food Biochem. 2019 Jul;43(7):e12846. doi: 10.1111/jfbc.12846. Epub 2019 Apr 1.

Abstract

Cyclic adenosine monophosphate (cAMP) plays an important role in modulating the activity of microbe cell. In this study, PKA (protein kinase A) activity was weakened through truncation of TPK2 promoter (-150 bp and -300 bp) and gene deletion of BCY1 (encodes the regulatory subunit of PKA), TPK1 and TPK3, generating strains BY9a-T2-150 and BY9a-T2-300, respectively. High-performance liquid chromatography analysis showed cAMP levels in BY9a-T2-150 and BY9a-T2-300 were increased by 5- and 18-fold, respectively, compared with that of parent strain, BY9a. The expression levels of TPK2 gene in two engineered strains were decreased by 95% and 97% compared with that of BY9a, respectively. The PKA activity reflected by heat resistance of engineered strains enhanced compared with parent strain BY9a. This study show a new method to increase the intracellular cAMP concentration in industrial yeast by fine-tuning of PKA activity, without influence in growth and fermentation properties. PRACTICAL APPLICATIONS: cAMP as the "second messenger," is essential for plant, animal, and microorganisms and human life. But its synthesis is still limited by expensive cost and time-consuming method. We constructed the industrial baker's yeast with high level of cAMP and desired to be used to produce functional food for relaxing smooth muscle, expanding blood vessels, improving liver function, and promoting nerve regeneration and as a food additive for treating hyperthyreosis and hepatopathy. The methods of two step homologous recombination and backcross operated in this study eliminate the exogenous gene in engineered strains, made it safety to be used in food production. Fine-tuning of PKA activity in engineered strains ensure produce high level of cAMP and exhibit normal growth performance in engineering strains. Therefore, this work is significant in functional foods product and has the potential to be used in practical application.

摘要

环磷酸腺苷(cAMP)在调节微生物细胞活性方面起着重要作用。在这项研究中,通过截断 TPK2 启动子(-150bp 和-300bp)和基因缺失 BCY1(编码 PKA 的调节亚基)、TPK1 和 TPK3,削弱了蛋白激酶 A(PKA)的活性,分别产生了菌株 BY9a-T2-150 和 BY9a-T2-300。高效液相色谱分析显示,与亲本菌株 BY9a 相比,BY9a-T2-150 和 BY9a-T2-300 中的 cAMP 水平分别增加了 5 倍和 18 倍。两个工程菌株中 TPK2 基因的表达水平分别比 BY9a 降低了 95%和 97%。与亲本菌株 BY9a 相比,工程菌株的耐热性反映的 PKA 活性增强。这项研究表明,通过精细调节 PKA 活性,为工业酵母增加细胞内 cAMP 浓度提供了一种新方法,而不会影响生长和发酵特性。

实际应用

cAMP 作为“第二信使”,对植物、动物和微生物以及人类生命至关重要。但其合成仍然受到昂贵成本和耗时方法的限制。我们构建了 cAMP 水平高的工业面包酵母,并希望将其用于生产用于放松平滑肌、扩张血管、改善肝功能、促进神经再生的功能性食品以及作为治疗甲状腺功能亢进和肝病的食品添加剂。本研究中两步同源重组和回交的方法消除了工程菌株中外源基因,使其在食品生产中更安全。工程菌株中 PKA 活性的精细调节确保了 cAMP 的高水平产生,并在工程菌株中表现出正常的生长性能。因此,这项工作在功能性食品产品中具有重要意义,并有可能在实际应用中使用。

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