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The NtrYX Two-Component System of Paracoccus denitrificans Is Required for the Maintenance of Cellular Iron Homeostasis and for a Complete Denitrification under Iron-Limited Conditions

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Author
Olaya-Abril, Alfonso
Luque-Almagro, Víctor Manuel
Hidalgo-Carrillo, J.
Chicano-Gálvez, Eduardo
Urbano, Francisco José
Moreno-Vivián, Conrado
Richardson, David J.
Roldán, María Dolores
Publisher
MDPI
Date
2022
Subject
Denitrification
Ferric uptake regulator
Iron homeostasis
Nitrate reduction
Nitrite reductase
Nitrous oxide reductase
NtrYX system
Paracoccus
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Abstract
Denitrification consists of the sequential reduction of nitrate to nitrite, nitric oxide, nitrous oxide, and dinitrogen. Nitrous oxide escapes to the atmosphere, depending on copper availability and other environmental factors. Iron is also a key element because many proteins involved in denitrification contain iron-sulfur or heme centers. The NtrYX two-component regulatory system mediates the responses in a variety of metabolic processes, including denitrification. A quantitative proteomic analysis of a Paracoccus denitrificans NtrY mutant grown under denitrifying conditions revealed the induction of different TonB-dependent siderophore transporters and proteins related to iron homeostasis. This mutant showed lower intracellular iron content than the wild-type strain, and a reduced growth under denitrifying conditions in iron-limited media. Under iron-rich conditions, it releases higher concentrations of siderophores and displayes lower nitrous oxide reductase (NosZ) activity than the wild-type, thus leading to nitrous oxide emission. Bioinformatic and qRT-PCR analyses revealed that NtrYX is a global transcriptional regulatory system that responds to iron starvation and, in turn, controls expression of the iron-responsive regulators fur, rirA, and iscR, the denitrification regulators fnrP and narR, the nitric oxide-responsive regulator nnrS, and a wide set of genes, including the cd1-nitrite reductase NirS, nitrate/nitrite transporters and energy electron transport proteins.
URI
http://hdl.handle.net/10396/23829
Fuente
International Journal of Molecular Sciences 23(16), 9172 (2022)
Versión del Editor
https://doi.org/10.3390/ijms23169172
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