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Chlamydomonas reinhardi

Erbes, D.L., King, D. and Gibbs, M. 1979. Inactivation of hydrogenase in cell-free extracts and whole cells of Chlamydomonas reinhardi by oxygen. Plant Physiol. 63, 1138-1142. [Pg.259]

Solter and Gibor [123] 1977 - - Chlamydomonas Reinhardi, mating process... [Pg.133]

Levine and Smillie (1962) used mutants of Chlamydomonas reinhardi to show clearly the separation of photoelectron transport into two phases, each with its own light reaction. Two mutant strains which are incapable of carrying out the Hill reaction are able to photoreduce NADP+ without oxygen evolution, provided they are supplied with electrons from an electron donor. Both mutants had an increased content of cytochrome f and a decreased content of plastoquinone. Presumably they are capable of performing the reactions carried out by System 1 only. [Pg.24]

Chironomus, 194 Chironomus melanotus, 116 Chlamydomonas reinhardi, 346 Chrysopa camea, 109 Chrysopa perla, 109 Chrysopa vittata, 109 Citellus lateralis, 374 Colymbetes fuscus, 109, 110 Cymbidium, 114... [Pg.489]

Schlapfer, P., Eichenberger, W. (1983) Evidence for the involvement of diacylglyceryl(N,N,N-trimethyl)homoserine in the desaturation of oleic and linoleic acids in ChLamydomonas reinhardi (Chlorophyceae). Plant Sci. Lett. 32 243-252. [Pg.60]

Chlamydomonas species have also been used in in vitro studies of the phenylurea herbicides. Loeppky and Tweedy (1969) observed that metobromuron was toxic to Chlamydomonas reinhardi and C. eugametos complete inhibition of growth occurring at 1.5 and 5.5 ppm, respectively. In heterothrophic growth studies, the herbicide was found to be as toxic to C. reinhardi as in autotrophic growth studies. This indicates that metobromuron, and possibly other phenylurea herbicides, inhibits algal growth not only by interference with photosynthesis but also by other routes. [Pg.10]

HODSON R.C., WILLIAMS S.K. and DAVIDSON W.R. 1975. Metabolic control of urea catabolism in Chlamydomonas reinhardi and Chlorella pyrenoidosa. Journal of Bacteriology, 121, 1022-1035. [Pg.216]

Fig. 36. Chlamydomonas reinhardi cell pulse-labeled for 10 minutes with acetate- H after 3.5 hours exposure to light The grains over the chloroplast are mosdy located over membranes. Label is seen also over mitochondria and protoplasm. X 13,000. (From Goldberg and Ohad, 1970, reproduced by permission of the authors and of the Editor of J. Cell Biol.)... Fig. 36. Chlamydomonas reinhardi cell pulse-labeled for 10 minutes with acetate- H after 3.5 hours exposure to light The grains over the chloroplast are mosdy located over membranes. Label is seen also over mitochondria and protoplasm. X 13,000. (From Goldberg and Ohad, 1970, reproduced by permission of the authors and of the Editor of J. Cell Biol.)...
Where are the genes for proteins of plastid ribosomes This is the problem we studied in Chlamydomonas reinhardi,... [Pg.226]

Chlamydomonas reinhardi is sensitive to the protein synthesis inhibitor, erythromycin. At the time, some erythromycin-resistant strains had been isolated and described, and we were considering experimental approaches to locate the sites of structural genes for proteins of plastid ribosomes. It seemed reasonable to use erythromycin resistance as a genetic marker if we could be certain that the antibiotic interacts with some part of the chloroplast ribosome and was not lethal for some other reason. Erythromycin was known to bind to the large subunit of Escherichia coli ribosomes, and the alteration leading to resistance in the bacteria was found to reside in a single protein in the 50 S subunit. ... [Pg.226]

Control of Chloroplast Membrane Biogenesis in Chlamydomonas reinhardi... [Pg.331]

Bar-Nun S, Schantz R and Chad I (1977) Appearance and composition of chlorophyll-protein complex I and II during chloroplast membrane biogenesis in Chlamydomonas reinhardi Y-1, Biochem. Biophys. Acta 459 451-467. [Pg.94]

Douglas M and Butow RA (1976) Variant translation products in yeast evidence for on mitochondrial DNA, Proc. Natl. Acad. Sci. USA 73 1083-1086. Nechushtai R and Nelson N (1981) Purification properties and biogenesis of chlamydomonas reinhardi photosystem I reaction center,... [Pg.94]

Merchant S, Shanir SL and Selman BR (1983) Molecular weight and subunit stoichiometry of the chlorlplast coupling factor 1 from chlamydomonas reinhardi, J. Biol. Chem. 258, 1026-1031. [Pg.509]

The chloroplast coupling factor one (CFj ) purified from Chlamydomonas reinhardi is a four subunit enzyme containing a, 3, Y and e subunits (Piccioni et al., 1981 Selman-Reimer et al., 1981). It was suggested by Piccioni et al. that the order of migration of the a and 3 subunits of the C. veinhardi CFi was reversed in comparison to that of spinach CFi. [Pg.583]

Piccioni RG, Bennoun P and Chua N-H (1981) A nuclear mutant of Chlamydomonas reinhardi defective in photosynthetic phosphorylation. Eur. J. Biochem. [Pg.586]

Selman-Reimer S, Merchant S, and Selman BR (1981) Isolation, purification, and characterization of coupling factor 1 from Chlamydomonas reinhardi. Biochemistry 20, 5476-5482,... [Pg.622]


See other pages where Chlamydomonas reinhardi is mentioned: [Pg.101]    [Pg.455]    [Pg.101]    [Pg.468]    [Pg.113]    [Pg.380]    [Pg.519]    [Pg.599]    [Pg.600]    [Pg.17]    [Pg.43]    [Pg.9]    [Pg.219]    [Pg.60]    [Pg.60]    [Pg.122]    [Pg.141]    [Pg.162]    [Pg.11]    [Pg.202]    [Pg.280]    [Pg.289]    [Pg.289]   
See also in sourсe #XX -- [ Pg.123 ]

See also in sourсe #XX -- [ Pg.17 , Pg.43 ]




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