Requirement for Asn298 on D1 protein for oxygen evolution

Analyses by exhaustive amino acid substitution in the green alga Chlamydomonas reinhardtii

Hiroshi Kuroda, Natsumi Kodama, Xiao Yu Sun, Shinichiro Ozawa, Yuichiro Takahashi

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

PSII generates strong oxidants used for water oxidation. The secondary electron donor, YZ, is Tyr161 on PSII reaction center D1 protein and mediates electron transfer from the oxygen-evolving Mn4CaO 5 cluster to the primary electron donor, P680. The latest PSII crystal structure revealed the presence of a hydrogen bond network around Y Z, which is anticipated to play important roles in the electron and proton transfer reactions. YZ forms a hydrogen bond with His190 which in turn forms a hydrogen bond with Asn298 on D1 protein. Although functional roles of YZ and His190 have already been characterized, little is known about the functional role of Asn298. Here we have generated 19 mutants from a green alga Chlamydomonas reinhardtii, in which the Asn298 has been substituted by each of the other 19 amino acid residues. All mutants showed significantly impaired or no photosynthetic growth. Seven mutants capable of photosynthetic growth showed oxygen-evolving activity although at a significantly reduced rate. Interestingly the oxygen-evolving activity of these mutants was markedly photosensitive. The 19 mutants accumulated PSII at variable levels and showed a light-induced electron transfer reaction from 1,5-diphenylcarbazide (DPC) to 2,6-dichlorophenolindophenol (DCIP), suggesting that Asn298 is important for the function and photoprotection of the Mn 4CaO5 cluster.

Original languageEnglish
Pages (from-to)1266-1275
Number of pages10
JournalPlant and Cell Physiology
Volume55
Issue number7
DOIs
Publication statusPublished - 2014

Fingerprint

Chlamydomonas reinhardtii
D1 protein
Chlorophyta
amino acid substitution
Amino Acid Substitution
Electrons
Oxygen
mutants
hydrogen
Hydrogen
electrons
Proteins
oxygen
electron transfer
Diphenylcarbazide
2,6-Dichloroindophenol
photostability
Growth
crystal structure
Oxidants

Keywords

  • Amino acid substitution
  • Chlamydomonas reinhardtii
  • D1 protein
  • Oxygen evolution
  • Photoinhibition
  • Photosystem II

ASJC Scopus subject areas

  • Plant Science
  • Physiology
  • Cell Biology
  • Medicine(all)

Cite this

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title = "Requirement for Asn298 on D1 protein for oxygen evolution: Analyses by exhaustive amino acid substitution in the green alga Chlamydomonas reinhardtii",
abstract = "PSII generates strong oxidants used for water oxidation. The secondary electron donor, YZ, is Tyr161 on PSII reaction center D1 protein and mediates electron transfer from the oxygen-evolving Mn4CaO 5 cluster to the primary electron donor, P680. The latest PSII crystal structure revealed the presence of a hydrogen bond network around Y Z, which is anticipated to play important roles in the electron and proton transfer reactions. YZ forms a hydrogen bond with His190 which in turn forms a hydrogen bond with Asn298 on D1 protein. Although functional roles of YZ and His190 have already been characterized, little is known about the functional role of Asn298. Here we have generated 19 mutants from a green alga Chlamydomonas reinhardtii, in which the Asn298 has been substituted by each of the other 19 amino acid residues. All mutants showed significantly impaired or no photosynthetic growth. Seven mutants capable of photosynthetic growth showed oxygen-evolving activity although at a significantly reduced rate. Interestingly the oxygen-evolving activity of these mutants was markedly photosensitive. The 19 mutants accumulated PSII at variable levels and showed a light-induced electron transfer reaction from 1,5-diphenylcarbazide (DPC) to 2,6-dichlorophenolindophenol (DCIP), suggesting that Asn298 is important for the function and photoprotection of the Mn 4CaO5 cluster.",
keywords = "Amino acid substitution, Chlamydomonas reinhardtii, D1 protein, Oxygen evolution, Photoinhibition, Photosystem II",
author = "Hiroshi Kuroda and Natsumi Kodama and Sun, {Xiao Yu} and Shinichiro Ozawa and Yuichiro Takahashi",
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TY - JOUR

T1 - Requirement for Asn298 on D1 protein for oxygen evolution

T2 - Analyses by exhaustive amino acid substitution in the green alga Chlamydomonas reinhardtii

AU - Kuroda, Hiroshi

AU - Kodama, Natsumi

AU - Sun, Xiao Yu

AU - Ozawa, Shinichiro

AU - Takahashi, Yuichiro

PY - 2014

Y1 - 2014

N2 - PSII generates strong oxidants used for water oxidation. The secondary electron donor, YZ, is Tyr161 on PSII reaction center D1 protein and mediates electron transfer from the oxygen-evolving Mn4CaO 5 cluster to the primary electron donor, P680. The latest PSII crystal structure revealed the presence of a hydrogen bond network around Y Z, which is anticipated to play important roles in the electron and proton transfer reactions. YZ forms a hydrogen bond with His190 which in turn forms a hydrogen bond with Asn298 on D1 protein. Although functional roles of YZ and His190 have already been characterized, little is known about the functional role of Asn298. Here we have generated 19 mutants from a green alga Chlamydomonas reinhardtii, in which the Asn298 has been substituted by each of the other 19 amino acid residues. All mutants showed significantly impaired or no photosynthetic growth. Seven mutants capable of photosynthetic growth showed oxygen-evolving activity although at a significantly reduced rate. Interestingly the oxygen-evolving activity of these mutants was markedly photosensitive. The 19 mutants accumulated PSII at variable levels and showed a light-induced electron transfer reaction from 1,5-diphenylcarbazide (DPC) to 2,6-dichlorophenolindophenol (DCIP), suggesting that Asn298 is important for the function and photoprotection of the Mn 4CaO5 cluster.

AB - PSII generates strong oxidants used for water oxidation. The secondary electron donor, YZ, is Tyr161 on PSII reaction center D1 protein and mediates electron transfer from the oxygen-evolving Mn4CaO 5 cluster to the primary electron donor, P680. The latest PSII crystal structure revealed the presence of a hydrogen bond network around Y Z, which is anticipated to play important roles in the electron and proton transfer reactions. YZ forms a hydrogen bond with His190 which in turn forms a hydrogen bond with Asn298 on D1 protein. Although functional roles of YZ and His190 have already been characterized, little is known about the functional role of Asn298. Here we have generated 19 mutants from a green alga Chlamydomonas reinhardtii, in which the Asn298 has been substituted by each of the other 19 amino acid residues. All mutants showed significantly impaired or no photosynthetic growth. Seven mutants capable of photosynthetic growth showed oxygen-evolving activity although at a significantly reduced rate. Interestingly the oxygen-evolving activity of these mutants was markedly photosensitive. The 19 mutants accumulated PSII at variable levels and showed a light-induced electron transfer reaction from 1,5-diphenylcarbazide (DPC) to 2,6-dichlorophenolindophenol (DCIP), suggesting that Asn298 is important for the function and photoprotection of the Mn 4CaO5 cluster.

KW - Amino acid substitution

KW - Chlamydomonas reinhardtii

KW - D1 protein

KW - Oxygen evolution

KW - Photoinhibition

KW - Photosystem II

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