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Alan Higbee

Researcher at University of Wisconsin-Madison

Publications -  22
Citations -  1469

Alan Higbee is an academic researcher from University of Wisconsin-Madison. The author has contributed to research in topics: Hydrolysate & Corn stover. The author has an hindex of 14, co-authored 22 publications receiving 1257 citations. Previous affiliations of Alan Higbee include Michigan State University & Great Lakes Bioenergy Research Center.

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Calorie Restriction and SIRT3 Trigger Global Reprogramming of the Mitochondrial Protein Acetylome

TL;DR: This work developed and applied a quantitative mass spectrometry method to probe the liver mitochondrial acetyl-proteome during CR versus control diet in mice that were wild-type or lacked the protein deacetylase SIRT3, and revealed widespread reprogramming of mitochondrial protein acetylation in response to CR.
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Cofermentation of glucose, xylose, and cellobiose by the beetle-associated yeast Spathaspora passalidarum.

TL;DR: Surprisingly, the ascomycetous, beetle-associated yeast Spathaspora passalidarum, which ferments xylose and cellobiose natively, can also coferment these two sugars in the presence of 30 g/liter glucose, making it very attractive for studying regulatory mechanisms enabling bioconversion of lignocellulosic materials by yeasts.
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Exploiting Natural Variation in Saccharomyces cerevisiae to Identify Genes for Increased Ethanol Resistance

TL;DR: This approach shows that comparative genomics across natural isolates can quickly identify genes for industrial engineering while expanding the understanding of natural diversity, by measuring acquired ethanol tolerance in a large panel of wild strains and showing that most strains can acquire higher tolerance after pretreatment.
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Decreased antigen-induced eicosanoid release in conjugated linoleic acid-fed guinea pigs.

TL;DR: It is shown that feeding CLA reduces lipid-derived inflammatory mediators produced by this type I hypersensitivity model, and decreased eicosanoid release from sensitized tissues in response to antigen challenge.