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利用高通量筛选在生物反应器中对工程假单胞菌进行高效芳香族转化为生物制品。

Engineering Pseudomonas putida for efficient aromatic conversion to bioproduct using high throughput screening in a bioreactor.

机构信息

Joint BioEnergy Institute, Lawrence Berkeley National Laboratory, 5885, Hollis Street, Emeryville, CA, USA; Biological Systems and Engineering Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Rd, Berkeley, CA, USA.

Biological Systems and Engineering Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Rd, Berkeley, CA, USA; Advanced Biofuels and Bioproducts Process Development Unit, Lawrence Berkeley National Laboratory, Hollis Street, Emeryville, CA, 5885, USA.

出版信息

Metab Eng. 2021 Jul;66:229-238. doi: 10.1016/j.ymben.2021.04.015. Epub 2021 May 6.

Abstract

Pseudomonas putida KT2440 is an emerging biomanufacturing host amenable for use with renewable carbon streams including aromatics such as para-coumarate. We used a pooled transposon library disrupting nearly all (4,778) non-essential genes to characterize this microbe under common stirred-tank bioreactor parameters with quantitative fitness assays. Assessing differential fitness values by monitoring changes in mutant strain abundance identified 33 gene mutants with improved fitness across multiple stirred-tank bioreactor formats. Twenty-one deletion strains from this subset were reconstructed, including GacA, a regulator, TtgB, an ABC transporter, and PP_0063, a lipid A acyltransferase. Thirteen deletion strains with roles in varying cellular functions were evaluated for conversion of para-coumarate, to a heterologous bioproduct, indigoidine. Several mutants, such as the ΔgacA strain improved fitness in a bioreactor by 35 fold and showed an 8-fold improvement in indigoidine production (4.5 g/L, 0.29 g/g, 23% of maximum theoretical yield) from para-coumarate as the carbon source.

摘要

恶臭假单胞菌 KT2440 是一种新兴的生物制造宿主,适用于可再生碳源,包括对香豆酸等芳香族化合物。我们使用了一个 pooled transposon library 来破坏几乎所有(4778 个)非必需基因,以便在常见的搅拌罐生物反应器参数下,使用定量适应性测定来对这种微生物进行特性描述。通过监测突变菌株丰度的变化来评估差异适应性值,确定了 33 个具有多个搅拌罐生物反应器格式适应性的基因突变体。从这个子集中重建了 21 个缺失菌株,包括 GacA(一种调节剂)、TtgB(一种 ABC 转运蛋白)和 PP_0063(一种脂酰转移酶)。评估了具有不同细胞功能的 13 个缺失菌株对异源生物产物靛蓝的对香豆酸的转化。一些突变体,如ΔgacA 菌株在生物反应器中的适应性提高了 35 倍,并且在以对香豆酸为碳源的情况下,靛蓝的产量提高了 8 倍(4.5 g/L,0.29 g/g,达到最大理论产量的 23%)。

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