Cationic substrates of soybean lipoxygenase-1 |
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Authors: | Chohany Lucas E Bishop Kathleen A Camic Hannah Sup Stephen J Findeis Peter M Clapp Charles H |
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Affiliation: | Department of Chemistry, Bucknell University, Lewisburg, PA 17837, United States |
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Abstract: | Soybean lipoxygenase-1 (SBLO-1) catalyzes the oxygenation of 1,4-dienes to produce conjugated diene hydroperoxides. The best substrates are anions of fatty acids; for example, linoleate is converted to 13(S)-hydroperoxy-9(Z),11(E)-octadecadienoate. The manner in which SBLO-1 binds substrates is uncertain. In the present work, it was found that SBLO-1 will oxygenate linoleyltrimethylammonium ion (LTMA) to give primarily13(S)-hydroperoxy-9(Z),11(E)-octadecadienyltrimethylammonium ion. The rate of this process is about the same at pH 7 and pH 9 and is about 30% of the rate observed with linoleate at pH 9. At pH 7, SBLO-1 oxygenates linoleyldimethylamine (LDMA) to give primarily 13(S)-hydroperoxy-9(Z),11(E)-octadecadienyldimethylamine. The oxygenation of LDMA occurs at about the same rate as LTMA at pH 7, but more slowly at pH 9. The results demonstrate that SBLO-1 will readily oxygenate substrates in which the carboxylate of linoleate is replaced with a cationic group, and the products of these reactions have the same stereo- and regiochemistry as the products obtained from fatty acid substrates. |
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Keywords: | BSTFA, N,O-bis(trimethylsilyl)trifluoroacetamide DBU, 1,8-diazabicyclo[5.4.0]undec-7-ene EIMS, electron-impact mass spectrometry ESI-MS, electrospray ionization mass spectrometry GC/MS, gas chromatography/mass spectrometry 13-HOD, 13(S)-hydroxy-9(Z),11(E)-octadecadienoate 13-HPOD, 13-(S)-hydroperoxy-9(Z),11(E)-octadecadienoate LDMA, linoleyldimethylamine LTMA, linoleyltrimethylammonium ion NMR, nuclear magnetic resonance SBLO-1, soybean lipoxygenase-1 TLC, thin layer chromatography |
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