Abstract

BackgroundDuring ethanol fermentation, the ethanologenic bacterium, Zymomonas mobilis may encounter several environmental stresses such as heat, ethanol and osmotic stresses due to high sugar concentration. Although supplementation of the compatible solute sorbitol into culture medium enhances cell growth of Z. mobilis under osmotic stress, the protective function of this compound on cell growth and ethanol production by this organism under other stresses such as heat and ethanol has not been described yet. The formation of sorbitol in Z. mobilis was carried out by the action of the glucose-fructose oxidoreductase (GFOR) enzyme which is regulated by the gfo gene. Therefore, the gfo gene in Z. mobilis was disrupted by the fusion-PCR-based construction technique in the present study, and the protective function of sorbitol on cell growth, protein synthesis and ethanol production by Z. mobilis under heat, ethanol, and osmotic stresses was investigated.ResultsBased on the fusion-PCR-based construction technique, the gfo gene in Z. mobilis was disrupted. Disruption of the Z. mobilis gfo gene resulted in the reduction of cell growth and ethanol production not only under osmotic stress but also under heat and ethanol stresses. Under these stress conditions, the transcription level of pdc, adhA, and adhB genes involved in the pyruvate-to-ethanol (PE) pathway as well as the synthesis of proteins particularly in Z. mobilis disruptant strain were decreased compared to those of the parent. These findings suggest that sorbitol plays a crucial role not only on cell growth and ethanol production but also on the protection of cellular proteins from stress responses.ConclusionWe showed for the first time that supplementation of the compatible solute sorbitol not only promoted cell growth but also increased the ethanol fermentation capability of Z. mobilis under heat, ethanol, and osmotic stresses. Although the molecular mechanism involved in tolerance to stress conditions after sorbitol supplementation is still unclear, this research has provided useful information for the development of the effective ethanol fermentation process particularly under environmental conditions with high temperature or high ethanol and sugar concentration conditions.

Highlights

  • Zymomonas mobilis, the Gram-negative facultative anaerobic bacterium, is unique in employing the Entner Doudoroff (ED) (2-keto-3-deoxy-6-phosphogluconate, KDPG), glyceraldehyde-3-phosphate-to-pyruvate (GP), and pyruvate-to-ethanol (PE) pathway for sugar catabolism and produces ethanol, and carbon dioxide as dominant fermentation products [1]

  • Among the kanamycin-resistant transformants obtained in this study, one isolate designated as Z. mobilis Δgfo was chosen for disruption analysis of the gfo gene

  • The nucleotide sequence of the Polymerase chain reaction (PCR) product from the parental strain showed a high degree of identity (99%) with the gfo gene in the Z. mobilis, confirming that this amplified DNA fragment was a part of the gfo gene in this microorganism

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Summary

Introduction

The Gram-negative facultative anaerobic bacterium, is unique in employing the Entner Doudoroff (ED) (2-keto-3-deoxy-6-phosphogluconate, KDPG), glyceraldehyde-3-phosphate-to-pyruvate (GP), and pyruvate-to-ethanol (PE) pathway for sugar catabolism and produces ethanol, and carbon dioxide as dominant fermentation products [1]. It possesses an incomplete Embden Meyerhof Parnas (EMP) pathway and an incomplete tricarboxylic acid cycle (TCA cycle) due to a lack of genes for 6-phosphofructokinase, 2-oxoglutarate dehydrogenase complex, and malate dehydrogenase [1,2,3], but possesses strong activities of the ED-GP pathway [4] Comparative studies of both laboratory- and pilot-scales on kinetics of batch fermentation of Z. mobilis versus a variety of yeast have indicated the suitability of Z. mobilis over yeasts due to the following advantages: its higher sugar uptake rate and ethanol yield (97% theoretical maximum yield), lower biomass production, and higher ethanol tolerance. The gfo gene in Z. mobilis was disrupted by the fusion-PCR-based construction technique in the present study, and the protective function of sorbitol on cell growth, protein synthesis and ethanol production by Z. mobilis under heat, ethanol, and osmotic stresses was investigated

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