Alternate routes to acetate tolerance lead to varied isoprenol production from mixed carbon sources in Pseudomonas putida.

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Guilherme M V de Siqueira, Aparajitha Srinivasan, Yan Chen, Jennifer W Gin, Christopher J Petzold, Taek Soon Lee, María-Eugenia Guazzaroni, Thomas Eng, Aindrila Mukhopadhyay
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引用次数: 0

Abstract

Lignocellulose is a renewable resource for the production of a diverse array of platform chemicals, including the biofuel isoprenol. Although this carbon stream provides a rich source of sugars, other organic compounds, such as acetate, can be used by microbial hosts. Here, we examined the growth and isoprenol production in a Pseudomonas putida strain pre-tolerized ("PT") background where its native isoprenol catabolism pathway is deleted, using glucose and acetate as carbon sources. We found that PT displays impaired growth in minimal medium containing acetate and often fails to grow in glucose-acetate medium. Using a mutant recovery-based approach, we generated tolerized strains that overcame these limitations, achieving fast growth and isoprenol production in the mixed carbon feed. Changes in the glucose and acetate assimilation routes, including an upregulation in PP_0154 (SpcC, succinyl-CoA:acetate CoA-transferase) and differential expression of the gluconate assimilation pathways, were key for higher isoprenol titers in the tolerized strains, whereas a different set of mechanisms were likely enabling tolerance phenotypes in media containing acetate. Among these, a coproporphyrinogen-III oxidase (HemN) was upregulated across all tolerized strains and in one isolate required for acetate tolerance. Utilizing a defined glucose and acetate mixture ratio reflective of lignocellulosic feedstocks for isoprenol production in P. putida allowed us to obtain insights into the dynamics and challenges unique to dual carbon source utilization that are obscured when studied separately. Together, this enabled the development of a P. putida bioconversion chassis able to use a more complex carbon stream to produce isoprenol.IMPORTANCEAcetate is a relatively abundant component of many lignocellulosic carbon streams and has the potential to be used together with sugars, especially in microbes with versatile catabolism such as P. putida. However, the use of mixed carbon streams necessitates additional optimization. Furthermore, the use of P. putida for the production of the biofuel target, isoprenol, requires the use of engineered strains that have additional growth and production constraints when cultivated in acetate and glucose mixtures. In this study, we generate acetate-tolerant P. putida strains that overcome these challenges and examine their ability to produce isoprenol. We show that acetate tolerance and isoprenol production, although independent phenotypes, can both be optimized in a given P. putida strain. Using proteomics and whole genome sequencing, we examine the molecular basis of both phenotypes and show that tolerance to acetate can occur via alternate routes and result in different impacts on isoprenol production.

在恶臭假单胞菌中,不同的醋酸耐受途径导致混合碳源产生不同的异戊二醇。
木质纤维素是一种可再生资源,用于生产各种平台化学品,包括生物燃料异戊二醇。虽然这种碳流提供了丰富的糖来源,但其他有机化合物,如醋酸盐,也可以被微生物宿主利用。在这里,我们研究了一种恶臭假单胞菌预耐受(“PT”)背景下的生长和异丙二醇的产生,在这种背景下,其天然的异丙二醇分解代谢途径被删除,以葡萄糖和醋酸盐作为碳源。我们发现,PT在含有乙酸的微量培养基中表现出生长受损,并且在葡萄糖-乙酸培养基中经常不能生长。使用基于突变体恢复的方法,我们产生了耐受性菌株,克服了这些限制,在混合碳饲料中实现了快速生长和异戊二醇生产。葡萄糖和醋酸盐同化途径的变化,包括PP_0154 (SpcC,琥珀酰辅酶a:醋酸辅酶a转移酶)的上调和葡萄糖酸盐同化途径的差异表达,是耐受性菌株异戊二醇滴度较高的关键,而在含乙酸的培养基中,可能有不同的机制使耐受性表型产生。其中,在所有耐受菌株和一株醋酸盐耐受所需菌株中,一种同比例卟啉原- iii氧化酶(HemN)均上调。利用确定的葡萄糖和醋酸盐混合物比例,反映了恶臭杆菌异戊二醇生产的木质纤维素原料,使我们能够深入了解双碳源利用的动态和独特挑战,这些动态和挑战在单独研究时是模糊不清的。总之,这使得恶臭杆菌生物转化底盘的开发能够使用更复杂的碳流来生产异戊二醇。重要性醋酸是许多木质纤维素碳流中相对丰富的成分,具有与糖一起使用的潜力,特别是在具有多种分解代谢的微生物中,如恶臭杆菌。然而,混合碳流的使用需要额外的优化。此外,使用恶臭杆菌生产生物燃料目标异戊二醇需要使用工程菌株,这些菌株在醋酸和葡萄糖混合物中培养时具有额外的生长和生产限制。在这项研究中,我们产生了耐醋酸盐的恶臭杆菌菌株,克服了这些挑战,并检查了它们产生异戊二醇的能力。我们表明,醋酸耐受性和异戊二醇生产,虽然独立的表型,都可以在给定的恶臭假单胞菌菌株优化。利用蛋白质组学和全基因组测序,我们研究了这两种表型的分子基础,并表明对醋酸盐的耐受性可以通过其他途径发生,并对异戊二醇的产生产生不同的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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