Literature DB >> 8144549

Regulation of heme oxygenase activity in Cyanidium caldarium by light, glucose, and phycobilin precursors.

G Rhie1, S I Beale.   

Abstract

Cyanobacteria, red algae, and cryptophytes contain phycobiliproteins which function as photosynthetic light-harvesting pigments. The chromophores of phycobiliproteins are phycobilins, open-chain tetrapyrroles that are synthesized from protoheme. The first step of phycobilin formation is the conversion of protoheme to biliverdin IX alpha in a reaction that is catalyzed by heme oxygenase. In the unicellular red alga, Cyanidium caldarium, light is required for the accumulation of phycobiliproteins. It has been reported previously that the synthesis of the apoprotein components of allophycocyanin and phycocyanin is induced by light in C. caldarium, that the phycobilin precursors, delta-aminolevulinic acid (ALA), protoporphyrin IX, and protoheme can substitute for light, and that the regulation is exerted at the level of mRNA synthesis. We have determined that a key enzyme of phycobilin formation is induced by light in C. caldarium. Extractable heme oxygenase activity is low in dark-grown cells, and it increases approximately 6-fold during the first 24 h after the cells are illuminated. After 24 h, the activity decreases to a level approximately equal to the initial activity. Heme oxygenase is induced in unilluminated cells by administration of ALA. D-Glucose, which is known to inhibit phycocyanin accumulation in C. caldarium, inhibits the induction of heme oxygenase by light or ALA. Induction of heme oxygenase by light or ALA is blocked by cycloheximide, an inhibitor of cytoplasmic protein synthesis, but not by chloramphenicol, an inhibitor of chloroplast protein synthesis. Rifampicin, an inhibitor of algal chloroplast RNA synthesis, and gabaculine, a competitive inhibitor of ALA biosynthesis, block the induction of heme oxygenase by light but not by ALA. These results indicate that heme oxygenase in C. caldarium is induced by phycobilin precursors. The induction by light and the repression of the induction by D-glucose are probably indirect effects mediated by the effects of light and D-glucose on phycobilin precursor formation. The results also indicate that heme oxygenase is encoded by a nuclear gene and is synthesized on cytoplasmic ribosomes.

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Year:  1994        PMID: 8144549

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  5 in total

1.  Differential transcription of phycobiliprotein components in Rhodella violacea. Light and nitrogen effects on the 33-kilodalton phycoerythrin rod linker polypeptide, phycocyanin, and phycoerythrin transcripts.

Authors:  C Lichtlé; F Garnier; C Bernard; G Zabulon; A Spilar; J C Thomas; A L Etienne
Journal:  Plant Physiol       Date:  1996-11       Impact factor: 8.340

2.  The heme oxygenase gene (pbsA) in the red alga Rhodella violacea is discontinuous and transcriptionally activated during iron limitation.

Authors:  C Richaud; G Zabulon
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-14       Impact factor: 11.205

3.  Heme oxygenase up-regulation in ultraviolet-B irradiated soybean plants involves reactive oxygen species.

Authors:  Gustavo G Yannarelli; Guillermo O Noriega; Alcira Batlle; Maria L Tomaro
Journal:  Planta       Date:  2006-05-16       Impact factor: 4.116

4.  Purification and identification of apophycocyanin alpha and beta subunits from soluble protein extracts of the red alga Cyanidium caldarium. Light exposure is not a prerequisite for biosynthesis of the protein moiety of this photosynthetic accessory pigment.

Authors:  L Turner; J D Houghton; S B Brown
Journal:  Planta       Date:  1997       Impact factor: 4.116

5.  External light conditions and internal cell cycle phases coordinate accumulation of chloroplast and mitochondrial transcripts in the red alga Cyanidioschyzon merolae.

Authors:  Yu Kanesaki; Sousuke Imamura; Ayumi Minoda; Kan Tanaka
Journal:  DNA Res       Date:  2012-04-19       Impact factor: 4.458

  5 in total

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