[Light-dependent carotenoid synthesis : II. Substitution of photoinduction by mercuribenzoate].

作者: W. Rau

DOI: 10.1007/BF00384847

关键词:

摘要: In the light-dependent carotenoid synthesis in Fusarium aquaeductuum photoinduction can be substituted by incubation of mycelium with SH-group poisons p-chloro-and p-hydroxymercuribenzoate dark. The minimum concentration both substances effective for induction is 5.10(-6) molar; maximal production pigments occurs at molar 5.10(-5)-10(-4). incubated mercuribenzoate, starts after a lagperiod 4-6 hours, increases until 24 hours addition poison and then continues some days constant rate. result that lag-period treatment mercuribenzoate much longer than it may due to fact presence respiration severely decreased (to 25% normal value concentrations 5.10(-5)) as consequence other metabolic processes are also depressed. From experiments which p-hydroxy-mercuribenzoate was removed different times washing distilled water, seen even an time only 2 induction. Other blocking do not induce synthesis; mercuring compounds benzoic acid ineffective.Carotenoid induced illumination or mercuri-benzoate quantitatively inhibited actidion (cycloheximid), potent inhibitor protein fungi. inhibition decreases increasing between beginning actidion; from this concluded reaction carotenogenic enzymes newly formed. If added 3 there almost no pigment production, indicating itself actidion.From these results light catalyse same chain regulatory mechanism, namely, SH-groups. We therefore assume function mechanism photooxydize SH-groups specific compound. Several possibilities compound site discussed.

参考文章(28)
F. T. Haxo, Some Biochemical Aspects of Fungal Carotenoids Springer Vienna. pp. 169- 197 ,(1955) , 10.1007/978-3-7091-7166-0_4
Malcolm R. Siegel, Hugh D. Sisler, Site of action of cycloheximide in cells of Saccharomyces pastorianus Biochimica et Biophysica Acta (BBA) - Specialized Section on Nucleic Acids and Related Subjects. ,vol. 87, pp. 70- 82 ,(1964) , 10.1016/0926-6550(64)90048-9
Donald L. Keister, Richard B. Hemmes, Pyridine nucleotide transhydrogenase from Chromatium. Journal of Biological Chemistry. ,vol. 241, pp. 2820- 2825 ,(1966) , 10.1016/S0021-9258(18)96537-3
E. C. Grob, The Biosynthesis of Carotenoids by Micro‐Organisms Ciba Foundation Symposium - Biosynthesis of Terpenes and Sterols. pp. 267- 278 ,(2009) , 10.1002/9780470719121.CH17
Luigi Casola, Philip E. Brumby, Vincent Massey, The Reversible Conversion of Lipoyl Dehydrogenase to an Artifactual Enzyme by Oxidation of Sulfhydryl Groups Journal of Biological Chemistry. ,vol. 241, pp. 4977- 4984 ,(1966) , 10.1016/S0021-9258(18)99659-6
Glenn A. Walker, Gordon L. Kilgour, Pyridine nucleotide oxidizing enzymes of Lactobacillus casei Archives of Biochemistry and Biophysics. ,vol. 111, pp. 534- 539 ,(1965) , 10.1016/0003-9861(65)90232-8
Luigi Casola, Vincent Massey, Differential Effects of Mercurial on the Lipoyl Reductase and Diaphorase Activities of Lipoyl Dehydrogenase Journal of Biological Chemistry. ,vol. 241, pp. 4985- 4993 ,(1966) , 10.1016/S0021-9258(18)99660-2