Abstract

Bacillus methanolicus MGA3 is a thermotolerant and relatively fast-growing methylotroph able to secrete large quantities of glutamate and lysine. These natural characteristics make B. methanolicus a good candidate to become a new industrial chassis organism, especially in a methanol-based economy. Intriguingly, the only substrates known to support B. methanolicus growth as sole sources of carbon and energy are methanol, mannitol, and, to a lesser extent, glucose and arabitol. Because fluxomics provides the most direct readout of the cellular phenotype, we hypothesized that comparing methylotrophic and nonmethylotrophic metabolic states at the flux level would yield new insights into MGA3 metabolism. In this study, we designed and performed a 13C metabolic flux analysis (13C-MFA) of the facultative methylotroph B. methanolicus MGA3 growing on methanol, mannitol, and arabitol to compare the associated metabolic states. On methanol, results showed a greater flux in the ribulose monophosphate (RuMP) pathway than in the tricarboxylic acid (TCA) cycle, thus validating previous findings on the methylotrophy of B. methanolicus New insights related to the utilization of cyclic RuMP versus linear dissimilation pathways and between the RuMP variants were generated. Importantly, we demonstrated that the linear detoxification pathways and the malic enzyme shared with the pentose phosphate pathway have an important role in cofactor regeneration. Finally, we identified, for the first time, the metabolic pathway used to assimilate arabitol. Overall, those data provide a better understanding of this strain under various environmental conditions.IMPORTANCE Methanol is inexpensive, is easy to transport, and can be produced both from renewable and from fossil resources without mobilizing arable lands. As such, it is regarded as a potential carbon source to transition toward a greener industrial chemistry. Metabolic engineering of bacteria and yeast able to efficiently consume methanol is expected to provide cell factories that will transform methanol into higher-value chemicals in the so-called methanol economy. Toward that goal, the study of natural methylotrophs such as Bacillus methanolicus is critical to understand the origin of their efficient methylotrophy. This knowledge will then be leveraged to transform such natural strains into new cell factories or to design methylotrophic capability in other strains already used by the industry.

Highlights

  • Bacillus methanolicus MGA3 is a thermotolerant and relatively fastgrowing methylotroph able to secrete large quantities of glutamate and lysine

  • While the lack of genetic tools must have impaired the development of new applications in the past [19], the establishment of gene expression tools based on theta and rolling-circle replicating plasmids has made B. methanolicus amenable to the overproduction of amino acids and their derivatives [18], and there is hope that recent breakthroughs from CRISPR interference (CRISPRi) will stimulate new innovations [20]

  • The operon responsible for arabitol assimilation in B. methanolicus consists of a phosphotransferase system (PTS) system (AtlABC) and two putative arabitol phosphate dehydrogenases (AtlD and AtlF) [22], which are chromosomally encoded and belong to the diverse superfamily of medium-chain dehydrogenases/ reductases (MDRs)

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Summary

Introduction

Bacillus methanolicus MGA3 is a thermotolerant and relatively fastgrowing methylotroph able to secrete large quantities of glutamate and lysine These natural characteristics make B. methanolicus a good candidate to become a new industrial chassis organism, especially in a methanol-based economy. We designed and performed a 13C metabolic flux analysis (13C-MFA) of the facultative methylotroph B. methanolicus MGA3 growing on methanol, mannitol, and arabitol to compare the associated metabolic states. We identified, for the first time, the metabolic pathway used to assimilate arabitol Overall, those data provide a better understanding of this strain under various environmental conditions. The study of natural methylotrophs such as Bacillus methanolicus is critical to understand the origin of their efficient methylotrophy This knowledge will be leveraged to transform such natural strains into new cell factories or to design methylotrophic capability in other strains already used by the industry. A flux-level description, which could validate previous findings and provide new insights into the msystems.asm.org 2

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