Interdependence of fucoxanthin biosynthesis and fucoxanthin-chlorophyll a/c binding proteins in Phaeodactylum tricornutum under different light intensities
Fucoxanthin (FX), a primary carotenoid, is associated with the fucoxanthin-chlorophyll a/c binding protein (FCP) complex integrated into the thylakoid membrane (TM) which functions as a light-harvesting complex in the diatom Phaeodactylum tricornutum. Here, we aimed to elucidate the FX production re...
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Veröffentlicht in: | Journal of applied phycology 2023-02, Vol.35 (1), p.25-42 |
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Sprache: | eng |
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Zusammenfassung: | Fucoxanthin (FX), a primary carotenoid, is associated with the fucoxanthin-chlorophyll a/c binding protein (FCP) complex integrated into the thylakoid membrane (TM) which functions as a light-harvesting complex in the diatom
Phaeodactylum tricornutum.
Here, we aimed to elucidate the FX production regulated by different light intensities via the correlation of FX biosynthesis and apoproteins composing of FCP complex. High light (HL) accelerated
P. tricornutum
growth more than low light (LL). The maximum values of FX content and productivity obtained under LL (1.7 mg g
−1
and 2.12 mg L
−1
day
−1
, respectively) were substantially higher than those obtained under HL (0.54 mg g
−1
and 0.79 mg L
−1
day
−1
, respectively). Notably, proteome and photosynthetic pigment analyses revealed the enrichment of FCP antennae in the LL culture TM fractions but not the HL culture. Semi-quantification of FCP antenna protein using LC–MS/MS and RNA transcriptome analyses revealed that
PtLhcf5
and
PtLhcf8
played crucial roles in FCP biosynthesis under LL.
P. tricornutum
cultured under light transition exhibited FCP formation only in the early growth stage to meet the increased photosynthetic activity requirements under LL. Meanwhile, FCP degradation could be triggered by HL throughout the cultivation period. Therefore, FX production was highly correlated with FCP formation, and LL conditions in the early growth stage were critical for higher FX productivity. |
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ISSN: | 0921-8971 1573-5176 |
DOI: | 10.1007/s10811-022-02856-2 |