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'Aldehydes' in keywords Facet   Publication Year 1992  [X]
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1992[X]
1Author    R. Jockers, R. D. SchmidRequires cookie*
 Title    Synthesis of Long-Chain Triazine Aldehydes -Substrates of Bacterial Luciferase and Photosynthetic Inhibitors  
 Abstract    S-triazines are photosynthetic inhibitors. They have been substituted with co-aminoundeca-noic acid. The coupling products have been transformed into triazine aldehydes. These com ­ pounds displace radioactive terbutryn and have inhibitory effects on photosynthesis in plants and bacteria. Triazine aldehydes were shown to be effective substrates for bacterial luciferase. A competitive assay between photosystem-II-herbicides and aldehyde-labeled triazines is dis­ cussed. 
  Reference    Z. Naturforsch. 47c, 573—5 (1992); received April 7/June 15 1992 
  Published    1992 
  Keywords    Herbicides, Bacterial Luciferase, Triazines, Aldehyde, Photosystem II, Biosensor 
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 TEI-XML for    default:Reihe_C/47/ZNC-1992-47c-0573.pdf 
 Identifier    ZNC-1992-47c-0573 
 Volume    47 
2Author    AkikazuH. Atanaka, T. Adahiko Kajiwara, Kenji Matsui, Hiromitsu ToyotaRequires cookie*
 Title    Substrate Specificity of Tea Leaf Hydroperoxide Lyase  
 Abstract    Substrate specificity o f tea leaf fatty acid hydroperoxide lyase was systematically investigat­ ed using an entire series o f co6-(5)-hydroperoxy-C14-C24 dienoic and trienoic acids as sub­ strates. Unexpectedly, the hydroperoxides o f C22 but not natural substrates, i.e., those o f C 18, showed the highest reactivities for the lyase. The reactivities o f the hydroperoxides o f trienoic acids were always four to ten times higher than those o f the dienoic acids. 
  Reference    Z. Naturforsch. 47c, 677—6 (1992); received June 24/July 24 1992 
  Published    1992 
  Keywords    Aldehyde, Fatty Acid Hydroperoxide, Hydroperoxide Lyase, Substrate Specificity, Tea Leaf 
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 TEI-XML for    default:Reihe_C/47/ZNC-1992-47c-0677.pdf 
 Identifier    ZNC-1992-47c-0677 
 Volume    47