Emiliania huxleyi endures N-limitation with an efficient metabolic budgeting and effective ATP synthesis

dc.contributor.authorRokitta, Sebastian D.
dc.contributor.authorDassow, Peter von
dc.contributor.authorRost, Björn.
dc.contributor.authorJohn, Uwe.
dc.date.accessioned2019-10-17T13:29:16Z
dc.date.available2019-10-17T13:29:16Z
dc.date.issued2014
dc.date.updated2019-10-14T18:31:26Z
dc.description.abstractAbstract Background Global change will affect patterns of nutrient upwelling in marine environments, potentially becoming even stricter regulators of phytoplankton primary productivity. To better understand phytoplankton nutrient utilization on the subcellular basis, we assessed the transcriptomic responses of the life-cycle stages of the biogeochemically important microalgae Emiliania huxleyi to nitrogen-limitation. Cells grown in batch cultures were harvested at ‘early’ and ‘full’ nitrogen-limitation and were compared with non-limited cells. We applied microarray-based transcriptome profilings, covering ~10.000 known E. huxleyi gene models, and screened for expression patterns that indicate the subcellular responses. Results The diploid life-cycle stage scavenges nitrogen from external organic sources and -like diatoms- uses the ornithine-urea cycle to rapidly turn over cellular nitrogen. The haploid stage reacts similarly, although nitrogen scavenging is less pronounced and lipid oxidation is more prominent. Generally, polyamines and proline appear to constitute major organic pools that back up cellular nitrogen. Both stages induce a malate:quinone-oxidoreductase that efficiently feeds electrons into the respiratory chain and drives ATP generation with reduced respiratory carbon throughput. Conclusions The use of the ornithine-urea cycle to budget the cellular nitrogen in situations of limitation resembles the responses observed earlier in diatoms. This suggests that underlying biochemical mechanisms are conserved among distant clades of marine phototrophic protists. The ornithine-urea cycle and proline oxidation appear to constitute a sensory-regulatory system that monitors and controls cellular nitrogen budgets under limitation. The similarity between the responses of the life-cycle stages, despite the usage of different genes, also indicates a strong functional consistency in the responses to nitrogen-limitation that appears to be owed to biochemical requirements. The malate:quinone-oxidoreductase is a genomic feature that appears to be absent from diatom genomes, and it is likely to strongly contribute to the uniquely high endurance of E. huxleyi under nutrient limitation.
dc.fuente.origenBiomed Central
dc.identifier.citationBMC Genomics. 2014 Dec 02;15(1):1051
dc.identifier.doi10.1186/1471-2164-15-1051
dc.identifier.urihttps://repositorio.uc.cl/handle/11534/26627
dc.issue.numeroNo. 1051
dc.language.isoen
dc.pagina.final14
dc.pagina.inicio1
dc.revistaBMC Genomicses_ES
dc.rightsacceso abierto
dc.rights.holderRokitta et al.; licensee BioMed Central Ltd.
dc.subject.ddc570
dc.subject.deweyBiologíaes_ES
dc.subject.otherMicroalgases_ES
dc.subject.otherAlgaes_ES
dc.subject.otherAlgas - Fisiologíaes_ES
dc.titleEmiliania huxleyi endures N-limitation with an efficient metabolic budgeting and effective ATP synthesises_ES
dc.typeartículo
dc.volumenVol. 15
sipa.codpersvinculados1009321
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