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Alan Collmer

Researcher at Cornell University

Publications -  172
Citations -  18990

Alan Collmer is an academic researcher from Cornell University. The author has contributed to research in topics: Pseudomonas syringae & Effector. The author has an hindex of 74, co-authored 171 publications receiving 18155 citations. Previous affiliations of Alan Collmer include University of Maryland, College Park & Washington State University.

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Pseudomonas syringae pv. syringae harpinPss: A protein that is secreted via the hrp pathway and elicits the hypersensitive response in plants

TL;DR: The ability of P. syringae to elicit the hypersensitive response in nonhost plants or pathogenesis in hosts is controlled by hrp genes, which encodes harpinPss, a 34.7 kd extracellular protein that elicits hypersensitive necrosis in tobacco and other plants.
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The Pseudomonas syringae Hrp pathogenicity island has a tripartite mosaic structure composed of a cluster of type III secretion genes bounded by exchangeable effector and conserved effector loci that contribute to parasitic fitness and pathogenicity in plants

TL;DR: DNA sequence analysis of the hrp/hrc regions in Psy 61, Psy B728a, and Pto DC3000 has revealed a Hrp pathogenicity island (Pai) with a tripartite mosaic structure, and deletion of a large portion of the CEL strongly reduces growth and abolishes pathogenicicity in tomato.
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An nptI-sacB-sacR cartridge for constructing directed, unmarked mutations in Gram-negative bacteria by marker exchange-eviction mutagenesis

TL;DR: The technique permits the construction of complex strains with many directed mutations without the introduction of a corresponding number of antibiotic resistance markers and should prove useful, for example, in exploring the role of the multiple pel genes in E. chrysanthemi.
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Bacterial Pathogens in Plants: Life up against the Wall.

TL;DR: A model for bacterial plant pathogenesis is developed based on the very recent third development-the discovery that the hrp genes encode a protein secretion system that has the potential to transfer virulence proteins into eukaryotic host cells.