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Algorithmic co-optimization of genetic constructs and growth conditions: application to 6-ACA, a potential nylon-6 precursor

机译:遗传构建体和生长条件的算法协同优化:应用于潜在的尼龙6前体6-ACA

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摘要

Optimizing bio-production involves strain and process improvements performed as discrete steps. However, environment impacts genotype and a strain that is optimal under one set of conditions may not be under different conditions. We present a methodology to simultaneously vary genetic and process factors, so that both can be guided by design of experiments (DOE). Advances in DNA assembly and gene insulation facilitate this approach by accelerating multi-gene pathway construction and the statistical interpretation of screening data. This is applied to a 6-aminocaproic acid (6-ACA) pathway in Escherichia coli consisting of six heterologous enzymes. A 32-member fraction factorial library is designed that simultaneously perturbs expression and media composition. This is compared to a 64-member full factorial library just varying expression (0.64 Mb of DNA assembly). Statistical analysis of the screening data from these libraries leads to different predictions as to whether the expression of enzymes needs to increase or decrease. Therefore, if genotype and media were varied separately this would lead to a suboptimal combination. This is applied to the design of a strain and media composition that increases 6-ACA from 9 to 48 mg/l in a single optimization step. This work introduces a generalizable platform to co-optimize genetic and non-genetic factors.
机译:优化生物生产涉及作为离散步骤执行的应变和过程改进。但是,环境影响基因型,在一组条件下最佳的菌株可能不在不同条件下。我们提出了一种同时改变遗传因素和过程因素的方法,以便可以通过实验设计(DOE)来指导两者。 DNA组装和基因绝缘方面的进展通过加速多基因途径的构建和筛选数据的统计解释而促进了这种方法。这适用于大肠杆菌中由6种异源酶组成的6-氨基己酸(6-ACA)途径。设计了一个32个成员的分数阶乘库,该库同时扰乱了表达和培养基组成。将此与仅改变表达(DNA装配的0.64 Mb)的64成员全因子文库进行比较。对来自这些文库的筛选数据的统计分析导致有关酶表达是否需要增加或减少的不同预测。因此,如果基因型和培养基分别变化,这将导致次优组合。这适用于在单个优化步骤中将6-ACA从9 mg / l增加到48 mg / l的菌株和培养基组成的设计。这项工作引入了一个可通用的平台来共同优化遗传和非遗传因素。

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