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用线性回归评估数值变量和有序变量对微生物合成产量的影响因素。

Evaluating factors that influence microbial synthesis yields by linear regression with numerical and ordinal variables.

机构信息

Department of Energy, Environmental and Chemical Engineering, Washington University, St. Louis, Missouri 63130, USA.

出版信息

Biotechnol Bioeng. 2011 Apr;108(4):893-901. doi: 10.1002/bit.22996. Epub 2010 Nov 30.

DOI:10.1002/bit.22996
PMID:21404262
Abstract

In the production of chemicals via microbial fermentation, achieving a high yield is one of the most important objectives. We developed a statistical model to analyze influential factors that determine product yield by compiling data obtained from engineered Escherichia coli developed within last 10 years. Using both numerical and ordinal variables (e.g., enzymatic steps, cultivation conditions, and genetic modifications) as input parameters, our model revealed that cultivation modes, nutrient supplementation, and oxygen conditions were the three significant factors for improving product yield. Generally, the model showed that product yield decreases as the number of enzymatic steps in the biosynthesis pathway increases (7-9% loss of yield per enzymatic step). Moreover, overexpression of enzymes or removal of competitive pathways (e.g., knockout) does not necessarily result in an amplification of product yield (P-value>0.1), possibly because of limited capacity in the biosynthesis pathway to accommodate an increase in flux. The model not only provides general guidelines for metabolic engineering and fermentation processes, but also allows a priori estimation and comparison of product yields under designed cultivation conditions.

摘要

在微生物发酵生产化学品的过程中,获得高产量是最重要的目标之一。我们开发了一种统计模型,通过编译过去 10 年中开发的工程大肠杆菌的数据来分析确定产品产量的影响因素。该模型将数值和序数变量(例如酶步骤、培养条件和遗传修饰)作为输入参数,结果表明培养模式、营养补充和氧气条件是提高产品产量的三个重要因素。一般来说,该模型表明,生物合成途径中的酶步骤数量增加会导致产品产量下降(每增加一个酶步骤,产量损失 7-9%)。此外,酶的过表达或去除竞争途径(例如敲除)不一定会导致产品产量的放大(P 值>0.1),这可能是由于生物合成途径的通量增加能力有限。该模型不仅为代谢工程和发酵过程提供了一般性指导,还允许在设计的培养条件下对产品产量进行先验估计和比较。

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