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在不同选择压力下重组酿酒酵母的稳定性研究。

Stability studies of recombinant Saccharomyces cerevisiae in the presence of varying selection pressure.

作者信息

Gupta Jagdish C, Mukherjee K J

机构信息

Centre for Biotechnology, Jawaharlal Nehru University, New Delhi, 110 067 India.

出版信息

Biotechnol Bioeng. 2002 Jun 5;78(5):475-88. doi: 10.1002/bit.10213.

Abstract

A recombinant yeast plasmid carrying the Ieu2 gene for auxotrophic complementation and a reporter gene for beta-galactosidase under the control of Gal10 promoter was studied in Saccharomyces cerevisiae. Growth, product formation, and plasmid stability were studied in defined, semi-defined, and complex media. The biomass concentration and specific activity were higher in complex medium than in defined medium, which was selective for the growth of plasmid-containing cells, leading to a 10-fold increase in volumetric activity. However, plasmid instability was very high in complex media with 50% plasmid-free cells emerging in the culture within 75 h of cultivation. In order to control instability, the growth rates of the plasmid-containing and plasmid-free cells were determined in semi-defined media, which consisted of defined medium supplemented with different concentrations of yeast extract. Below a critical concentration of yeast extract (0.05 g/L), the plasmid-containing cells had a growth rate advantage over the plasmid-free cells. This was possibly because, at this concentration of yeast extract, the availability of leucine became the rate-determining factor in the specific growth rate of plasmid-free cells. A feeding strategy was designed which maintained a low concentration of the residual yeast extract in the medium and thus continuously provided the plasmid-containing cells with a competitive advantage over the plasmid-free cells. This resulted in high stability as well as high cell density under non-selective conditions, which led to a 10-fold increase in the volumetric activity compared to that achieved in defined selective media. A simple mathematical model was formulated to verify the experimental data. The important state variables and process parameters, i.e., biomass concentration, beta-galactosidase expression, sucrose consumption, yeast extract consumption, and specific growth rates of the two cell populations, were evaluated. These variables and parameters along with the differential equations based on material balances as well as the experimental results obtained were used in a mathematical model for the fed-batch cultivation. These correctly verified the experimental data and clearly illustrated the concept behind the success of the fed-batch strategy under yeast extract starvation.

摘要

在酿酒酵母中研究了一种携带用于营养缺陷型互补的Leu2基因和在Gal10启动子控制下的β-半乳糖苷酶报告基因的重组酵母质粒。在限定培养基、半限定培养基和复合培养基中研究了生长、产物形成和质粒稳定性。复合培养基中的生物量浓度和比活性高于限定培养基,限定培养基对含质粒细胞的生长具有选择性,导致体积活性增加10倍。然而,在复合培养基中质粒不稳定性非常高,在培养75小时内培养物中出现50%不含质粒的细胞。为了控制不稳定性,在半限定培养基中测定了含质粒细胞和不含质粒细胞的生长速率,半限定培养基由添加不同浓度酵母提取物的限定培养基组成。低于酵母提取物的临界浓度(0.05 g/L)时,含质粒细胞比不含质粒细胞具有生长速率优势。这可能是因为,在这个酵母提取物浓度下,亮氨酸的可用性成为不含质粒细胞比生长速率的速率决定因素。设计了一种补料策略,该策略维持培养基中残留酵母提取物的低浓度,从而持续为含质粒细胞提供相对于不含质粒细胞的竞争优势。这导致在非选择性条件下具有高稳定性以及高细胞密度,与在限定选择性培养基中相比,体积活性增加了10倍。建立了一个简单的数学模型来验证实验数据。评估了重要的状态变量和过程参数,即生物量浓度、β-半乳糖苷酶表达、蔗糖消耗、酵母提取物消耗以及两个细胞群体的比生长速率。这些变量和参数以及基于物料平衡的微分方程以及获得的实验结果被用于分批补料培养的数学模型中。这些正确地验证了实验数据,并清楚地说明了在酵母提取物饥饿条件下分批补料策略成功背后的概念。

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