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John E. Cronan

Researcher at University of Illinois at Urbana–Champaign

Publications -  390
Citations -  28125

John E. Cronan is an academic researcher from University of Illinois at Urbana–Champaign. The author has contributed to research in topics: Escherichia coli & Acyl carrier protein. The author has an hindex of 90, co-authored 381 publications receiving 26467 citations. Previous affiliations of John E. Cronan include University of Adelaide & University of Cambridge.

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Detecting and characterizing N-acyl-homoserine lactone signal molecules by thin-layer chromatography

TL;DR: The assay can be used to screen cultures of bacteria for acyl-homoserine lactones, for quantifying the amounts of these molecules produced, and as an analytical and preparative aid in determining the structures of these signal molecules.

Detecting and characterizing N-acyl-homoserine lactone signal molecules by thin-layer chromatography (autoinductionysignaling systemsyquorum sensingygene regulationydetection systems)

TL;DR: In this paper, the authors used thin-layer chromatography with detection using Agrobacterium tumefa-ciens harboring lacZ fused to a gene that is regulated by autoinduction.
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Regulation of fatty acid biosynthesis in Escherichia coli.

TL;DR: This review focuses on four major areas of research on the fatty acid synthesis pathway of E. coli, and the genes encoding many of these proteins have been cloned, and characterization of these genes has led to a better understanding of the pathway.
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Acyl homoserine-lactone quorum-sensing signal generation

TL;DR: An analysis of the patterns of product inhibition indicated that RhlI catalyzes signal synthesis by a sequential, ordered reaction mechanism in which S-adenosylmethionine binds toRhlI as the initial step in the enzymatic mechanism.
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Cyclopropane ring formation in membrane lipids of bacteria.

TL;DR: Manipulation of the CFA synthase of Escherichia coli by genetic methods has nevertheless provided valuable insight into the physiology of CFA formation and identified the C FA synthase gene as one of several rpoS-regulated genes of E. coli and provided for the construction of strains in which proposed cellular functions of CFAs can be properly evaluated.