Literature DB >> 3096777

Formation of lipoxin B by the pure reticulocyte lipoxygenase.

H Kühn, R Wiesner, L Alder, T Schewe, H Stender.   

Abstract

The pure reticulocyte lipoxygenase converts 5,15-DiHETE via a lipoxygenase reaction to 5,14,15-trihydroxy-6,8,10,12-eicosatetraenoic acid (a lipoxin B isomer) as shown by GC/MS analysis of its trimethylsilyl ether. With arachidonic acid, 15-HETE and 15-HETE methyl ester this lipoxin B isomer was also formed. The results presented here indicate that pure mammalian lipoxygenases are able to form lipoxins via sequential multiple oxygenation of arachidonic acid or its hydroxy derivatives.

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Year:  1986        PMID: 3096777     DOI: 10.1016/0014-5793(86)81026-2

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  3 in total

1.  Kinetic and structural investigations into the allosteric and pH effect on the substrate specificity of human epithelial 15-lipoxygenase-2.

Authors:  Netra Joshi; Eric K Hoobler; Steven Perry; Giovanni Diaz; Brian Fox; Theodore R Holman
Journal:  Biochemistry       Date:  2013-10-30       Impact factor: 3.162

Review 2.  Lipoxins: eicosanoids carrying intra- and intercellular messages.

Authors:  C N Serhan
Journal:  J Bioenerg Biomembr       Date:  1991-02       Impact factor: 2.945

3.  Transformations of 5-HETE by activated keratinocyte 15-lipoxygenase and the activation mechanism.

Authors:  F A Green
Journal:  Lipids       Date:  1990-10       Impact factor: 1.880

  3 in total

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