Metal utilization in genome-reduced bacteria: Do human mycoplasmas rely on iron?
ABC, ATP-binding cassette
ECF transporter
ECF, energy-coupling factor
Fur, ferric uptake regulator
Hrl, histidine-rich lipoprotein
Iron homeostasis
Metal acquisition
Metalloenzyme
Mge, Mycoplasma genitalium
Mho, Mycoplasma hominis
Mollicutes
Mpe, Mycoplasma penetrans
Mpn, Mycoplasma pneumonia
Mycoplasmas
PDB, protein data bank
RNR, ribonucleotide reductase
XRF, X-ray fluorescence
ZIP, zinc-iron permease
Journal
Computational and structural biotechnology journal
ISSN: 2001-0370
Titre abrégé: Comput Struct Biotechnol J
Pays: Netherlands
ID NLM: 101585369
Informations de publication
Date de publication:
2021
2021
Historique:
received:
30
06
2021
revised:
08
10
2021
accepted:
12
10
2021
entrez:
12
11
2021
pubmed:
13
11
2021
medline:
13
11
2021
Statut:
epublish
Résumé
Mycoplasmas are parasitic bacteria with streamlined genomes and complex nutritional requirements. Although iron is vital for almost all organisms, its utilization by mycoplasmas is controversial. Despite its minimalist nature, mycoplasmas can survive and persist within the host, where iron availability is rigorously restricted through nutritional immunity. In this review, we describe the putative iron-enzymes, transporters, and metalloregulators of four relevant human mycoplasmas. This work brings in light critical differences in the mycoplasma-iron interplay.
Identifiants
pubmed: 34765092
doi: 10.1016/j.csbj.2021.10.022
pii: S2001-0370(21)00444-X
pmc: PMC8566771
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
5752-5761Informations de copyright
© 2021 The Authors.
Déclaration de conflit d'intérêts
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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