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. 1995 Aug;108(4):1657–1664. doi: 10.1104/pp.108.4.1657

Isolation and Characterization of a Protein Associated with Carotene Globules in the Alga Dunaliella bardawil.

A Katz 1, C Jimenez 1, U Pick 1
PMCID: PMC157547  PMID: 12228570

Abstract

The halotolerant alga Dunaliella bardawil accumulates very large amounts of [beta]-carotene when exposed to high light intensity. The accumulated [beta]-carotene is concentrated in small, oily globules within the chloroplast and has been suggested to protect the alga against photodamage by high irradiation (A. Ben-Amotz, A. Katz, M. Avron [1982] J Phycol 18:529-537;A. Ben-Amotz, M. Avron [1983] Plant Physiol 72: 593-597; A. Ben-Amotz, A. Shaish, M. Avron [1989] Plant Physiol 91: 1040-1043). A 38-kD protein was identified and purified from [beta]-carotene globules and was designated carotene globule protein (Cgp). Induction of Cgp occurs in parallel with [beta]-carotene accumulation in D. bardawil grown under different inductive conditions. Cgp is overproduced in a constitutive mutant strain that overproduces [beta]-carotene and is not detected in Dunaliella salina, a species that does not accumulate [beta]-carotene. Cgp production was not suppressed by norflurazon, an inhibitor of [beta]-carotene synthesis that leads to accumulation of the carotenoid precursor phytoene. Immunogold-labeling analysis by electron microscopy demonstrates that the protein is localized at the periphery of the globules. Proteolytic cleavage by trypsin enhances the coalescence and destruction of the globules, in parallel with Cgp disappearance. It is suggested that the function of Cgp is to stabilize the structure of the globules within the chloroplast.

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Selected References

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