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Chlorophyll bleaching

Cells grown in dark, i.e., are colorless (bleached - chlorophyll free) but have both stigma and paraflagellar body. [Pg.69]

Mutant induced with streptomycin treatments bleached (chlorophyll free) cells without stigma but possessing paraflagellar body. [Pg.69]

Por colour change efiects in green the writer uses chlorophyll —it being very easily bleached. Chlorophyll is the green colouring matter of plants. [Pg.32]

Green coloration, present in many vegetable oils, poses a particular problem in oil extracted from immature or damaged soybeans. Chlorophyll is the compound responsible for this defect. StmcturaHy, chlorophyll is composed of a porphyrin ring system, in which magnesium is the central metal atom, and a phytol side chain which imparts a hydrophobic character to the stmcture. Conventional bleaching clays are not as effective for removal of chlorophylls as for red pigments, and specialized acid-activated adsorbents or carbon are required. [Pg.124]

Bleaching Herbicides. Membrane-based modes of herbicidal action relevant to photosynthesis (37) include those of inhibitors of carotenoid biosynthesis, eg, norflura2on, diftmon, y -phenoxyben2amines inhibitors of chlorophyll biosynthesis, eg, oxadia2on, DTP or... [Pg.43]

Fats and Oils. The oxidation of fats and oils in food products can be prevented by the addition of citric acid to chelate the trace metals that catalyze the oxidation. Citric acid is also used in the bleaching clays and the degumming process during oil refining to remove chlorophyll and phosphohpids (59—63). [Pg.185]

D. D. Brooks and co-workers, "The Synergistic Effect of Neutral Bleaching Clay and Citric Acid Chlorophyll Removal," paper presented at the... [Pg.188]

The molecular target site of triketone herbicides is the enzyme -hydroxyphenylpyruvate dioxygenase (HPPD). Inhibition of this enzyme disrupts the biosynthesis of carotenoids and causes a bleaching (loss of chlorophyll) effect on the foliage similar to that observed with inhibitors ofphytoene desaturase (e.g. norflurazon). However, the mechanism of action of HPPD inhibitors is different. Inhibtion of HPPD stops the synthesis of homogen tisate (HGA), which is a key precursor of the 8 different tocochromanols (tocopherols and tocotrienols) and prenyl quinones. In the absence of prenylquinone plastoquinone, phytoene desaturase activity is interrupted. The bleaching of the green tissues ensues as if these compounds inhibited phytoene desaturase. [Pg.240]

The photooxidation of chlorophyll indicated in Eq. 23-31 is accompanied by bleaching in the principal light absorption band. However, since there is so much light-gathering chlorophyll for each reaction center, the effect is small. The study of the process has been aided greatly by preparation of isolated bacterial photochemical reaction centers. [Pg.1310]

Fig. 9. The absorption spectra of chlorophyll a in its ground singlet (broken line) and its bleached state. See ref. 79. Fig. 9. The absorption spectra of chlorophyll a in its ground singlet (broken line) and its bleached state. See ref. 79.

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See also in sourсe #XX -- [ Pg.192 ]




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