Abstract

Diatoms are a major group of primary producers ubiquitous in all aquatic ecosystems. To protect themselves from photooxidative damage in a fluctuating light climate potentially punctuated with regular excess light exposures, diatoms have developed several photoprotective mechanisms. The xanthophyll cycle (XC) dependent non-photochemical chlorophyll fluorescence quenching (NPQ) is one of the most important photoprotective processes that rapidly regulate photosynthesis in diatoms. NPQ depends on the conversion of diadinoxanthin (DD) into diatoxanthin (DT) by the violaxanthin de-epoxidase (VDE), also called DD de-epoxidase (DDE). To study the role of DDE in controlling NPQ, we generated transformants of P. tricornutum in which the gene (Vde/Dde) encoding for DDE was silenced. RNA interference was induced by genetic transformation of the cells with plasmids containing either short (198 bp) or long (523 bp) antisense (AS) fragments or, alternatively, with a plasmid mediating the expression of a self-complementary hairpin-like construct (inverted repeat, IR). The silencing approaches generated diatom transformants with a phenotype clearly distinguishable from wildtype (WT) cells, i.e. a lower degree as well as slower kinetics of both DD de-epoxidation and NPQ induction. Real-time PCR based quantification of Dde transcripts revealed differences in transcript levels between AS transformants and WT cells but also between AS and IR transformants, suggesting the possible presence of two different gene silencing mediating mechanisms. This was confirmed by the differential effect of the light intensity on the respective silencing efficiency of both types of transformants. The characterization of the transformants strengthened some of the specific features of the XC and NPQ and confirmed the most recent mechanistic model of the DT/NPQ relationship in diatoms.

Highlights

  • Diatoms belong to the most abundant photosynthetic microorganisms on Earth accounting for about 40% of the primary production in the oceans [1]

  • The xanthophyll de-epoxidation is mediated by an enzyme, the deepoxidase, which is located in the lumen of the thylakoids, while the back-conversion is ensured by a stromal epoxidase [8,9,10]

  • Expression in P. tricornutum A Violaxanthin De-epoxidase (Vde) gene encoding a protein related to the violaxanthin deepoxidase (VDE) of higher plants (Phatr2 ID 44635) has been identified in the genome of P. tricornutum [15,16]

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Summary

Introduction

Diatoms belong to the most abundant photosynthetic microorganisms on Earth accounting for about 40% of the primary production in the oceans [1]. The light-dependent build-up of the transthylakoidal proton gradient (DpH) and the subsequent acidification of the lumen is necessary for the binding of the de-epoxidase to the thylakoid membrane in order to get access to its xanthophyll substrate [8,9]. This process is regulated by the protonation of a glutamic acid-rich domain located in the highly charged C-terminal part of the enzyme and by the protonation of histidine residues located in the lipocalin region [11,12,13]. The pigments of the Vx cycle are precursors of DD and DT, and of the main LHC xanthophyll, fucoxanthin [9,10]

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