Plant Physiology Preview Published on April 10, 2003; 10.1104/pp.102.019620
Received December 21, 2002
Returned for revision January 28, 2003
Accepted February 17, 2003
Role of the Reversible Xanthophyll Cycle in the Photosystem II Damage and Repair Cycle in Dunaliella salina
EonSeon Jin , Kittisak Yokthongwattana , Juergen E.W. Polle , and Anastasios Melis *
Department of Plant and Microbial Biology, 111 Koshland Hall, University of California, Berkeley, California 94720-3102
* Corresponding author; email: melis{at}nature.berkeley.edu.
The Dunaliella salina photosynthetic apparatus organization and function was investigated in wild type (WT) and a mutant (zea1) lacking all , -epoxycarotenoids derived from zeaxanthin (Z). The zea1 mutant lacked antheraxanthin, violaxanthin, and neoxanthin from its thylakoid membranes but constitutively accumulated Z instead. It also lacked the so-called xanthophyll cycle, which, upon irradiance stress, reversibly converts violaxanthin to Z via a de-epoxidation reaction. Despite the pronounced difference observed in the composition of , -epoxycarotenoids between WT and zea1, no discernible difference could be observed between the two strains in terms of growth, photosynthesis, organization of the photosynthetic apparatus, photo-acclimation, sensitivity to photodamage, or recovery from photo-inhibition. WT and zea1 were probed for the above parameters over a broad range of growth irradiance and upon light shift experiments (low light to high light shift and vice versa). A constitutive accumulation of Z in the zea1 strain did not affect the acclimation of the photosynthetic apparatus to irradiance, as evidenced by indistinguishable irradiance-dependent adjustments in the chlorophyll antenna size and photosystem content of WT and zea1 strain. In addition, a constitutive accumulation of Z in the zea1 strain did not affect rates of photodamage or the recovery of the photosynthetic apparatus from photo-inhibition. However, Z in the WT accumulated in parallel with the accumulation of photodamaged PSII centers in the chloroplast thylakoids and decayed in tandem with a chloroplast recovery from photo-inhibition. These results suggest a role for Z in the protection of photodamaged and disassembled PSII reaction centers, apparently needed while PSII is in the process of degradation and replacement of the D1/32-kD reaction center protein.
This article has been cited by other articles:

|
 |

|
 |
 
M. Heddad, H. Noren, V. Reiser, M. Dunaeva, B. Andersson, and I. Adamska
Differential Expression and Localization of Early Light-Induced Proteins in Arabidopsis
Plant Physiology,
September 1, 2006;
142(1):
75 - 87.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Hirashima, S. Satoh, R. Tanaka, and A. Tanaka
Pigment Shuffling in Antenna Systems Achieved by Expressing Prokaryotic Chlorophyllide a Oxygenase in Arabidopsis
J. Biol. Chem.,
June 2, 2006;
281(22):
15385 - 15393.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. D. Hieber, O. Kawabata, and H. Y. Yamamoto
Significance of the Lipid Phase in the Dynamics and Functions of the Xanthophyll Cycle as Revealed by PsbS Overexpression in Tobacco and In-vitro De-epoxidation in Monogalactosyldiacylglycerol Micelles
Plant Cell Physiol.,
January 15, 2004;
45(1):
92 - 102.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. Bergantino, A. Segalla, A. Brunetta, E. Teardo, F. Rigoni, G. M. Giacometti, and I. Szabo
Light- and pH-dependent structural changes in the PsbS subunit of photosystem II
PNAS,
December 9, 2003;
100(25):
15265 - 15270.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|
|