Abstract

Hungateiclostridium thermocellum ATCC 27405 is a promising bacterium for consolidated bioprocessing with a robust ability to degrade lignocellulosic biomass through a multienzyme cellulosomal complex. The bacterium uses the released cellodextrins, glucose polymers of different lengths, as its primary carbon source and energy. In contrast, the bacterium exhibits poor growth on monosaccharides such as fructose and glucose. This phenomenon raises many important questions concerning its glycolytic pathways and sugar transport systems. Until now, the detailed mechanisms of H. thermocellum adaptation to growth on hexose sugars have been relatively poorly explored. In this study, adaptive laboratory evolution was applied to train the bacterium in hexose sugars-based media, and genome resequencing was used to detect the genes that got mutated during adaptation period. RNA-seq data of the first culture growing on either fructose or glucose revealed that several glycolytic genes in the Embden–Mayerhof–Parnas pathway were expressed at lower levels in these cells than in cellobiose-grown cells. After seven consecutive transfer events on fructose and glucose (~42 generations for fructose-adapted cells and ~40 generations for glucose-adapted cells), several genes in the EMP glycolysis of the evolved strains increased the levels of mRNA expression, accompanied by a faster growth, a greater biomass yield, a higher ethanol titer than those in their parent strains. Genomic screening also revealed several mutation events in the genomes of the evolved strains, especially in those responsible for sugar transport and central carbon metabolism. Consequently, these genes could be applied as potential targets for further metabolic engineering to improve this bacterium for bio-industrial usage.

Highlights

  • FAs1 and GAs1 was still lower than that of CGs1, in contrast to the results obtained in the work of Johnson et al [29], who found that the final H. thermocellum cell density of FAs1, GAs1 and CGs1 was comparable

  • The observed GAs1 enzyme activities were in agreement with a study by Zhang et al [28], who used kinetic models and empirical experiments to prove that glucose was an inhibitor of the H. thermocellum cellulosome

  • This study indicated that the phosphofructokinase (PFK)- and phosphoglycerate mutase (PGAM)-encoding genes were downregulated under ethanol stress conditions, in agreement with what was observed for FAs1 and GAs1 under nutritional stress in the present study (Figure 4)

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Summary

Introduction

Microorganisms 2021, 9, 1445 have been performed to expand our knowledge of H. thermocellum genetics, gene expression, metabolism, and physiology. Improving the utilization of glucose by H. thermocellum is beneficial for cellulosic bioethanol production. The chemical formula of glucose and fructose is the same, differences in their molecular formations leads to changes in cellulase production of glucose- and fructose-adapted cells. This phenomenon was first observed by Johnson et al [29] decades ago, it has not been elucidated on a point of view of mRNA expression level

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