Literature DB >> 28315315

Connectivity among Photosystem II centers in phytoplankters: Patterns and responses.

Kui Xu1, Jessica L Grant-Burt1, Natalie Donaher1, Douglas A Campbell2.   

Abstract

Fast Repetition and Relaxation chlorophyll fluorescence induction is used to estimate the effective absorption cross section of PSII (σPSII), to analyze phytoplankton acclimation and electron transport. The fitting coefficient ρ measures excitation transfer from closed PSII to remaining open PSII upon illumination, which could theoretically generate a progressive increase in σPSII for the remaining open PSII. To investigate how ρ responds to illumination we grew marine phytoplankters with diverse antenna structures (Prochlorococcus, Synechococcus, Ostreococcus and Thalassiosira pseudonana) under limiting or saturating growth light. Initial ρ varied with growth light in Synechococcus and Thalassiosira. With increasing actinic illumination PSII closed progressively and ρ decreased for all four taxa, in a pattern explicable as an exponential decay of ρ with increasing distance between remaining open PSII reaction centers. This light-dependent down-regulation of ρ allows the four phytoplankters to limit the effect of increasing light upon σPSII. The four structurally distinct taxa showed, however, distinct rates of response of ρ to PSII closure, likely reflecting differences in the spacing or orientation among their PSII centers. Following saturating illumination recovery of ρ in darkness coincided directly with PSII re-opening in Prochlorococcus. Even after PSII had re-opened in Synechococcus a transition to State II slowed dark recovery of ρ. In Ostreococcus sustained NPQ slowed dark recovery of ρ. In Thalassiosira dark recovery of ρ was slowed, possibly by a light-induced change in PSII spacing. These patterns of ρ versus PSII closure are thus a convenient probe of comparative PSII spacings.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Fast Repetition and Relaxation chlorophyll fluorescence induction; Light acclimation; Ostreococcus; Photosynthesis; Phytoplankton; Prochlorococcus; Synechococcus; Thalassiosira pseudonana

Mesh:

Substances:

Year:  2017        PMID: 28315315     DOI: 10.1016/j.bbabio.2017.03.003

Source DB:  PubMed          Journal:  Biochim Biophys Acta Bioenerg        ISSN: 0005-2728            Impact factor:   3.991


  4 in total

1.  Time-dependent upregulation of electron transport with concomitant induction of regulated excitation dissipation in Haslea diatoms.

Authors:  R Perkins; C Williamson; J Lavaud; J-L Mouget; D A Campbell
Journal:  Photosynth Res       Date:  2018-04-16       Impact factor: 3.573

2.  Lhcx proteins provide photoprotection via thermal dissipation of absorbed light in the diatom Phaeodactylum tricornutum.

Authors:  Jochen M Buck; Jonathan Sherman; Carolina Río Bártulos; Manuel Serif; Marc Halder; Jan Henkel; Angela Falciatore; Johann Lavaud; Maxim Y Gorbunov; Peter G Kroth; Paul G Falkowski; Bernard Lepetit
Journal:  Nat Commun       Date:  2019-09-13       Impact factor: 14.919

3.  Nitrogen starvation induces distinct photosynthetic responses and recovery dynamics in diatoms and prasinophytes.

Authors:  Justin D Liefer; Aneri Garg; Douglas A Campbell; Andrew J Irwin; Zoe V Finkel
Journal:  PLoS One       Date:  2018-04-11       Impact factor: 3.240

4.  Different functional traits among closely related algal symbionts dictate stress endurance for vital Indo-Pacific reef-building corals.

Authors:  Kenneth D Hoadley; Daniel T Pettay; Allison Lewis; Drew Wham; Chris Grasso; Robin Smith; Dustin W Kemp; Todd LaJeunesse; Mark E Warner
Journal:  Glob Chang Biol       Date:  2021-08-02       Impact factor: 13.211

  4 in total

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