Enzymatic formation of bilirubin.
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Biomedical subjects
Publications and source records attributed to R F Troxler.
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Plastid development in albescent (al/al) and wild-type (+/al) strains of Zea mays has been studied in the electron microscope. Etiolated seedlings of the mutant are severely deficient in colored carotenoid pigments and accumulate carotenoid precursors tentatively identified as phytoene and phytofluene. The fine structure of proplastids in etiolated wild-type and mutant leaves is similar with 1 notable exception. Osmiophilic bodies found in the wild-type were lacking in all sections of albescent proplastids examined suggesting that these structures may be storage centers for carotenoid pigments. Plastid pigments are destroyed, chlorophyll synthesizing potential is lost, and the ultrastructure of plastids is irreversibly altered when mutant seedlings are placed directly in high intensity light. However, synthesis of plastid pigments and development of the photosynthetic apparatus as seen in the electron microscope is normal, and indistinguishable from that in the wild-type, in seedlings of the albescent mutant preilluminated with low intensity light prior to high intensity illumination. During treatment in low intensity light carotenogenesis is initiated in the mutant and proceeds normally thereafter.
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The synthesis of chlorophyll a and the bile-pigment and protein moieties of phycocyanin were arrested in illuminated cells of Cyanidium caldarium, strain III-D-2, incubated with chloramphenicol, ethionine, p-fluorophenylalanine, and p-chloromercuribenzoate. Pigment synthesis was similarly retarded in illuminated cells provided with nutrient medium lacking nitrogen.Porphobilinogen, porphyrins, and a blue phycobilin were excreted into the nutrient medium by illuminated and unilluminated cells of wild-type and mutant C. caldarium strains incubated with delta-aminolevulinic acid in darkness. Pigment production from delta-aminolevulinic acid was sensitive to treatment with chloramphenicol and ethionine. Cells of C. caldarium excreted 7 red-fluorescing porphyrins into the suspending medium during incubation with delta-aminolevulinic acid. Three of these porphyrins were identified as uroporphyrin III, coproporphyrin III, and protoporphyrin on the basis of their spectral properties and by paper chromatogaphy with standards. The blue phycobilin was characterized spectrally and compared with biliverdin. The algal phycobilin displayed properties of a pigment with a violin-type structure. The phycobilin may be an immediate precursor of phycocyanobilin, the phycocyanin chromophore, or identical to it.
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