The plastid proteome of the nonphotosynthetic chlorophycean alga Polytomella parva.

Amyloplast Chlamydomonas reinhardtii Chlorophycean algae Nonphotosynthetic algae Plastid proteome Polytomella parva

Journal

Microbiological research
ISSN: 1618-0623
Titre abrégé: Microbiol Res
Pays: Germany
ID NLM: 9437794

Informations de publication

Date de publication:
Feb 2021
Historique:
received: 22 07 2020
revised: 23 10 2020
accepted: 13 11 2020
pubmed: 8 12 2020
medline: 17 7 2021
entrez: 7 12 2020
Statut: ppublish

Résumé

The unicellular, free-living, nonphotosynthetic chlorophycean alga Polytomella parva, closely related to Chlamydomonas reinhardtii and Volvox carteri, contains colorless, starch-storing plastids. The P. parva plastids lack all light-dependent processes but maintain crucial metabolic pathways. The colorless alga also lacks a plastid genome, meaning no transcription or translation should occur inside the organelle. Here, using an algal fraction enriched in plastids as well as publicly available transcriptome data, we provide a morphological and proteomic characterization of the P. parva plastid, ultimately identifying several plastid proteins, both by mass spectrometry and bioinformatic analyses. Data are available via ProteomeXchange with identifier PXD022051. Altogether these results led us to propose a plastid proteome for P. parva, i.e., a set of proteins that participate in carbohydrate metabolism; in the synthesis and degradation of starch, amino acids and lipids; in the biosynthesis of terpenoids and tetrapyrroles; in solute transport and protein translocation; and in redox homeostasis. This is the first detailed plastid proteome from a unicellular, free-living colorless alga.

Identifiants

pubmed: 33285428
pii: S0944-5013(20)30517-6
doi: 10.1016/j.micres.2020.126649
pii:
doi:

Substances chimiques

Amino Acids 0
Proteome 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

126649

Informations de copyright

Copyright © 2020. Published by Elsevier GmbH.

Auteurs

Emma O Fuentes-Ramírez (EO)

Departamento de Genética Molecular, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, CDMX, Mexico. Electronic address: efuentes0300@gmail.com.

Miriam Vázquez-Acevedo (M)

Departamento de Genética Molecular, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, CDMX, Mexico. Electronic address: mvazquez@ifc.unam.mx.

Alfredo Cabrera-Orefice (A)

Radboud Institute for Molecular Life Sciences, Department of Pediatrics, Radboud University Medical Center, Geert Grooteplein-Zuid 10, 6525, GA, Nijmegen, the Netherlands. Electronic address: alfredbiomed@gmail.com.

Sergio Guerrero-Castillo (S)

Radboud Institute for Molecular Life Sciences, Department of Pediatrics, Radboud University Medical Center, Geert Grooteplein-Zuid 10, 6525, GA, Nijmegen, the Netherlands; University Children's Research@Kinder-UKE, University Medical Center Hamburg-Eppendorf, 20246, Hamburg, Germany. Electronic address: s.guerrerocastillo@uke.de.

Diego González-Halphen (D)

Departamento de Genética Molecular, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, CDMX, Mexico. Electronic address: dhalphen@ifc.unam.mx.

Articles similaires

Humans Arthritis, Rheumatoid Lipid Metabolism Male Female
Humans Induced Pluripotent Stem Cells Schizophrenia Neural Stem Cells DNA Damage

Classifications MeSH