4.5 Article

Structure to function of an α-glucan metabolic pathway that promotes Listeria monocytogenes pathogenesis

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NATURE MICROBIOLOGY
卷 2, 期 2, 页码 -

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NATURE RESEARCH
DOI: 10.1038/nmicrobiol.2016.202

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资金

  1. National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Department of Health and Human Services [HHSN272200700058C, HHSN272201200026C]
  2. NIH [R01 AI083241, AI083241-03S1, F32 AI 115954]
  3. US Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
  4. Michigan Technology Tri-Corridor [085P1000817]
  5. Northwestern University High Throughput Analysis Laboratory
  6. Northwestern University Keck Biophysics Facility
  7. Cancer Center Support [NCI CA060553]
  8. Michigan Economic Development Corporation

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Here we employ a 'systems structural biology' approach to functionally characterize an unconventional a-glucan metabolic pathway from the food-borne pathogen Listeria monocytogenes (Lm). Crystal structure determination coupled with basic biochemical and biophysical assays allowed for the identification of anabolic, transport, catabolic and regulatory portions of the cycloalternan pathway. These findings provide numerous insights into cycloalternan pathway function and reveal the mechanism of repressor, open reading frame, kinase (ROK) transcription regulators. Moreover, by developing a structural overview we were able to anticipate the cycloalternan pathway's role in the metabolism of partially hydrolysed starch derivatives and demonstrate its involvement in Lm pathogenesis. These findings suggest that the cycloalternan pathway plays a role in interspecies resource competition-potentially within the host gastrointestinal tract- and establish the methodological framework for characterizing bacterial systems of unknown function.

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