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Hydrogen peroxide as an alternate substrate for the oxygen-evolving complex

dc.contributor.authorFrasch, Wayne D.en_US
dc.contributor.authorMei, Ruien_US
dc.date.accessioned2006-04-07T19:55:37Z
dc.date.available2006-04-07T19:55:37Z
dc.date.issued1987-03-25en_US
dc.identifier.citationFrasch, Wayne D., Mei, Rui (1987/03/25)."Hydrogen peroxide as an alternate substrate for the oxygen-evolving complex." Biochimica et Biophysica Acta (BBA) - Bioenergetics 891(1): 8-14. <http://hdl.handle.net/2027.42/26767>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T1S-47RS4X0-P9/2/3c8f2a57858cbb5aa75d86443b1f37f1en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/26767
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3103684&dopt=citationen_US
dc.description.abstractPhotosystem II reaction centers evolve O2 in the dark when H2O2 is added as a substrate. Although some of this activity can be attributed to catalase, as much as 75% of the activity was not affected by the addition of 1 mM KCN. Several lines of evidence demonstrate that this KCN-insensitive O2 evolution from H2O2 in the dark is catalyzed by the cycling of S states in the oxygen-evolving complex including: (1) inactivation of H2O2-mediated O2 evolution by Ca/EDTA washing; (2) susceptibility of the activity to inhibition by amines like ammonia and Tris; (3) inhibition by CCCP which is known to accelerate the rate of deactivation of the S2 state and; (4) a direct dependence of the rate of O2 evolution on the presence of calcium and (5) chloride.en_US
dc.format.extent534649 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleHydrogen peroxide as an alternate substrate for the oxygen-evolving complexen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Biological Sciences, The University of Michigan, Ann Arbor, MI, U.S.A.en_US
dc.contributor.affiliationumDivision of Biological Sciences, The University of Michigan, Ann Arbor, MI, U.S.A.en_US
dc.identifier.pmid3103684en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/26767/1/0000319.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0005-2728(87)90077-6en_US
dc.identifier.sourceBiochimica et Biophysica Actaen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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