ZfN: Search Results

1	Author	R. Jockers, R. D. Schmid	Requires 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

2	Author	AkikazuH. Atanaka, T. Adahiko Kajiwara, Kenji Matsui, Hiromitsu Toyota	Requires 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