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Photosynth Res. 2017 Sep;133(1-3):117-127. doi: 10.1007/s11120-017-0370-2. Epub 2017 Mar 24.

In vivo system for analyzing the function of the PsbP protein using Chlamydomonas reinhardtii.

Author information

1
Graduate School of Biostudies, Kyoto University, Sakyo, Kyoto, 606-8502, Japan.
2
Graduate School of Biostudies, Kyoto University, Sakyo, Kyoto, 606-8502, Japan. ifuku@kais.kyoto-u.ac.jp.

Abstract

The PsbP protein is an extrinsic subunit of photosystem II (PSII) specifically developed in green-plant species including land plants and green algae. The protein-protein interactions involving PsbP and its effect on oxygen evolution have been investigated in vitro using isolated PSII membranes. However, the importance of those interactions needs to be examined at the cellular level. To this end, we developed a system expressing exogenous PsbP in the background of the Chlamydomonas BF25 mutant lacking native PsbP. Expression of His-tagged PsbP successfully restored the oxygen-evolving activity and photoautotrophic growth of the mutant, while PsbP-∆15 lacking the N-terminal 15 residues, which are crucial for the oxygen-evolving activity of spinach PSII in vitro, only partially did. This demonstrated the importance of N-terminal sequence of PsbP for the photosynthetic activity in vivo. Furthermore, the PSII-LHCII supercomplex can be specifically purified from the Chlamydomonas cells having His-tagged PsbP using a metal affinity chromatography. This study provides a platform not only for the functional analysis of PsbP in vivo but also for structural analysis of the PSII-LHCII supercomplex from green algae.

KEYWORDS:

Chlamydomonas reinhardtii; His-tag; Photosystem II; PsbP

PMID:
28341915
DOI:
10.1007/s11120-017-0370-2
[Indexed for MEDLINE]

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