期刊
NEW PHYTOLOGIST
卷 204, 期 3, 页码 507-520出版社
WILEY-BLACKWELL
DOI: 10.1111/nph.12926
关键词
C-4 metabolism; fatty acid metabolism; glycine decarboxylase; marine diatoms; quantitative proteomics; pentose phosphate pathway; pyruvate phosphate dikinase (PPDK); pyruvate carboxylase
资金
- National Science Foundation (NSF) [OCE 0526365, OCE 0526188, OCE 0927733]
The mechanisms of carbon concentration in marine diatoms are controversial. At low CO2, decreases in O-2 evolution after inhibition of phosphoenolpyruvate carboxylases (PEPCs), and increases in PEPC transcript abundances, have been interpreted as evidence for a C-4 mechanism in Thalassiosira pseudonana, but the ascertainment of which proteins are responsible for the subsequent decarboxylation and PEP regeneration steps has been elusive. We evaluated the responses of T.pseudonana to steady-state differences in CO2 availability, as well as to transient shifts to low CO2, by integrated measurements of photosynthetic parameters, transcript abundances and quantitative proteomics. On shifts to low CO2, two PEPC transcript abundances increased and then declined on timescales consistent with recoveries of F-v/F-m, non-photochemical quenching (NPQ) and maximum chlorophyll a-specific carbon fixation (P-max), but transcripts for archetypical decarboxylation enzymes phosphoenolpyruvate carboxykinase (PEPCK) and malic enzyme (ME) did not change. Of 3688 protein abundances measured, 39 were up-regulated under low CO2, including both PEPCs and pyruvate carboxylase (PYC), whereas ME abundance did not change and PEPCK abundance declined. We propose a closed-loop biochemical model, whereby T.pseudonana produces and subsequently decarboxylates a C-4 acid via PEPC2 and PYC, respectively, regenerates phosphoenolpyruvate (PEP) from pyruvate in a pyruvate phosphate dikinase-independent (but glycine decarboxylase (GDC)-dependent) manner, and recuperates photorespiratory CO2 as oxaloacetate (OAA).
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