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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003524naa a2200421 4500
001oai:DiVA.org:umu-81861
003SwePub
008131022s2011 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-818612 URI
024a https://doi.org/10.1007/s00018-010-0571-82 DOI
040 a (SwePub)umu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Cava, Felipeu Channing Laboratory, Brigham and Women’s Hospital, Harvard Medical School, and Howard Hughes Medical Institute, Boston, USA4 aut0 (Swepub:umu)feca0003
2451 0a Emerging knowledge of regulatory roles of D-amino acids in bacteria
264 c 2010-12-14
264 1b Springer Science and Business Media LLC,c 2011
338 a electronic2 rdacarrier
520 a The D-enantiomers of amino acids have been thought to have relatively minor functions in biological processes. While L-amino acids clearly predominate in nature, D-amino acids are sometimes found in proteins that are not synthesized by ribosomes, and D-Ala and D-Glu are routinely found in the peptidoglycan cell wall of bacteria. Here, we review recent findings showing that D-amino acids have previously unappreciated regulatory roles in the bacterial kingdom. Many diverse bacterial phyla synthesize and release D-amino acids, including D-Met and D-Leu, which were not previously known to be made. These noncanonical D-amino acids regulate cell wall remodeling in stationary phase and cause biofilm dispersal in aging bacterial communities. Elucidating the mechanisms by which D-amino acids govern cell wall remodeling and biofilm disassembly will undoubtedly reveal new paradigms for understanding how extracytoplasmic processes are regulated as well as lead to development of novel therapeutics.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinsk bioteknologix Medicinsk bioteknologi0 (SwePub)304012 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Medical Biotechnologyx Medical Biotechnology0 (SwePub)304012 hsv//eng
653 a D-amino acid
653 a racemase
653 a stationary phase
653 a peptidoglycan
653 a biofilm
653 a regulation
700a Lam, Hubertu Channing Laboratory, Brigham and Women’s Hospital, Harvard Medical School, and Howard Hughes Medical Institute, Boston, USA4 aut
700a de Pedro, Miguel Au Centro de Biología Molecular "Severo Ochoa" Consejo Superior de Investigaciones Científicas, Universidad Autónoma de Madrid, Spain4 aut
700a Waldor, Matthew Ku Channing Laboratory, Brigham and Women’s Hospital, Harvard Medical School, and Howard Hughes Medical Institute, Boston, USA4 aut
710a Channing Laboratory, Brigham and Women’s Hospital, Harvard Medical School, and Howard Hughes Medical Institute, Boston, USAb Centro de Biología Molecular "Severo Ochoa" Consejo Superior de Investigaciones Científicas, Universidad Autónoma de Madrid, Spain4 org
773t Cellular and Molecular Life Sciences (CMLS)d : Springer Science and Business Media LLCg 68:5, s. 817-831q 68:5<817-831x 1420-682Xx 1420-9071
856u https://umu.diva-portal.org/smash/get/diva2:658605/FULLTEXT01.pdfx primaryx Raw objecty fulltext:print
856u https://link.springer.com/content/pdf/10.1007%2Fs00018-010-0571-8.pdf
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-81861
8564 8u https://doi.org/10.1007/s00018-010-0571-8

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Cava, Felipe
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