Abstract

BackgroundIsobutanol can be a better biofuel than ethanol due to its higher energy density and lower hygroscopicity. Furthermore, the branched-chain structure of isobutanol gives a higher octane number than the isomeric n-butanol. Saccharomyces cerevisiae was chosen as the production host because of its relative tolerance to alcohols, robustness in industrial fermentations, and the possibility for future combination of isobutanol production with fermentation of lignocellulosic materials.ResultsThe yield of isobutanol was improved from 0.16 to 0.97 mg per g glucose by simultaneous overexpression of biosynthetic genes ILV2, ILV3, and ILV5 in valine metabolism in anaerobic fermentation of glucose in mineral medium in S. cerevisiae. Isobutanol yield was further improved by twofold by the additional overexpression of BAT2, encoding the cytoplasmic branched-chain amino-acid aminotransferase. Overexpression of ILV6, encoding the regulatory subunit of Ilv2, in the ILV2 ILV3 ILV5 overexpression strain decreased isobutanol production yield by threefold. In aerobic cultivations in shake flasks in mineral medium, the isobutanol yield of the ILV2 ILV3 ILV5 overexpression strain and the reference strain were 3.86 and 0.28 mg per g glucose, respectively. They increased to 4.12 and 2.4 mg per g glucose in yeast extract/peptone/dextrose (YPD) complex medium under aerobic conditions, respectively.ConclusionsOverexpression of genes ILV2, ILV3, ILV5, and BAT2 in valine metabolism led to an increase in isobutanol production in S. cerevisiae. Additional overexpression of ILV6 in the ILV2 ILV3 ILV5 overexpression strain had a negative effect, presumably by increasing the sensitivity of Ilv2 to valine inhibition, thus weakening the positive impact of overexpression of ILV2, ILV3, and ILV5 on isobutanol production. Aerobic cultivations of the ILV2 ILV3 ILV5 overexpression strain and the reference strain showed that supplying amino acids in cultivation media gave a substantial improvement in isobutanol production for the reference strain, but not for the ILV2 ILV3 ILV5 overexpression strain. This result implies that other constraints besides the enzyme activities for the supply of 2-ketoisovalerate may become bottlenecks for isobutanol production after ILV2, ILV3, and ILV5 have been overexpressed, which most probably includes the valine inhibition to Ilv2.

Highlights

  • Isobutanol can be a better biofuel than ethanol due to its higher energy density and lower hygroscopicity

  • We studied overexpression of the genes ILV2, ILV3, ILV5, ILV6, and BAT2, involved in valine metabolism, in different combinations, and investigated the isobutanol production in the constructed strains

  • Improvement of anaerobic isobutanol production by overexpression of genes in valine metabolism To overexpress the genes, ILV2, ILV3, and ILV5, which encode the catalysts for the conversion of pyruvate to 2ketoisovalerate, the coding regions were fused with the S. cerevisiae PGK1 promoter

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Summary

Introduction

Isobutanol can be a better biofuel than ethanol due to its higher energy density and lower hygroscopicity. Microbial production of chemicals to be used as liquid biofuels will allow the use of renewable raw materials such as lignocellulose. The chemical properties of ethanol, such as a high tendency to absorb water, are not optimal for all purposes. For many purposes, such as a jet fuel, improved properties are required with regard to hygroscopicity and energy density. Higher alcohols, such as n-butanol and isobutanol, represent possible alternatives. Compared with n-butanol, isobutanol has the advantage of having a higher octane number, and the possibility of usage outside the fuel industry as well [1]

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