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William W. Metcalf

Researcher at University of Illinois at Urbana–Champaign

Publications -  167
Citations -  11242

William W. Metcalf is an academic researcher from University of Illinois at Urbana–Champaign. The author has contributed to research in topics: Methanosarcina acetivorans & Methanosarcina. The author has an hindex of 57, co-authored 156 publications receiving 9737 citations. Previous affiliations of William W. Metcalf include Purdue University & Howard Hughes Medical Institute.

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The Genome of M. Acetivorans Reveals Extensive Metabolic and Physiological Diversity

James E. Galagan, +76 more
- 01 Apr 2002 - 
TL;DR: The complete genome sequence of an acetate-utilizing methanogen, Methanosarcina acetivorans C2A, is reported, which indicates the likelihood of undiscovered natural energy sources for methanogenesis, whereas the presence of single-subunit carbon monoxide dehydrogenases raises the possibility of nonmethanogenic growth.
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Conditionally replicative and conjugative plasmids carrying lacZ alpha for cloning, mutagenesis, and allele replacement in bacteria.

TL;DR: Several new cloning vectors for mutagenesis and allele replacement experiments are described, including plasmids that have the R6K gamma DNA replication origin so they replicate only in bacteria supplying the pi replication protein, and which also encode a positive counterselectable marker.
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A roadmap for natural product discovery based on large-scale genomics and metabolomics

TL;DR: Extrapolation from the 830-genome dataset reveals that Actinobacteria encode hundreds of thousands of future drug leads, while the strong correlation between phylogeny and GCFs frames a roadmap to efficiently access them.
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Genetic analysis of pigment biosynthesis in Xanthobacter autotrophicus Py2 using a new, highly efficient transposon mutagenesis system that is functional in a wide variety of bacteria.

TL;DR: A highly efficient method of transposon mutagenesis was developed for genetic analysis of Xanthobacter autotrophicus Py2 and preliminary results from other laboratories have confirmed the effectiveness of this method in additional phylogenetically diverse species.