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David J. Leak

Researcher at University of Bath

Publications -  127
Citations -  9692

David J. Leak is an academic researcher from University of Bath. The author has contributed to research in topics: Fermentation & Chemistry. The author has an hindex of 31, co-authored 118 publications receiving 8681 citations. Previous affiliations of David J. Leak include University of Warwick & National Technical University.

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The path forward for biofuels and biomaterials

TL;DR: The integration of agroenergy crops and biorefinery manufacturing technologies offers the potential for the development of sustainable biopower and biomaterials that will lead to a new manufacturing paradigm.
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Ionic liquid pretreatment of lignocellulosic biomass with ionic liquid–water mixtures

TL;DR: In this paper, ground lignocellulosic biomass (Miscanthus giganteus, pine (Pinus sylvestris) and willow (Salix viminalis) was pretreated with ionic liquid-water mixtures of 1-butyl-3methylimidazolium methyl sulfate and 1- butyl- 3methyloridehydrogensulfate hydrogen sulfate.
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Copper stress underlies the fundamental change in intracellular location of methane mono-oxygenase in methane-oxidizing organisms: Studies in batch and continuous cultures

TL;DR: Results indicated that the copper effect could explain a similar switch in intracellular location observed in Methylosinus trichosporium OB3b but that some methanotrophs do not have the capacity to overcome copper stress in this way.
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The effect of the ionic liquid anion in the pretreatment of pine wood chips

TL;DR: In this article, the effect of the anion of ionic liquids on air-dried pine (Pinus radiata) has been investigated and it was shown that 1-butyl-3methylimidazolium dicyanamide dissolves neither cellulose nor lignocellulosic material.
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Metabolic engineering of Geobacillus thermoglucosidasius for high yield ethanol production.

TL;DR: The metabolic engineering of two strains of Geobacillus thermoglucosidasius to divert their fermentative carbon flux from a mixed acid pathway, to one in which ethanol becomes the major product, which involved elimination of the lactate dehydrogenase and pyruvate formate lyase pathways.