Nitrogen regulation of protein–protein interactions and transcript levels of GlnK PII regulator and AmtB ammonium transporter homologs in Archaea

Please use this identifier to cite or link to this item:
Información del item - Informació de l'item - Item information
Title: Nitrogen regulation of protein–protein interactions and transcript levels of GlnK PII regulator and AmtB ammonium transporter homologs in Archaea
Authors: Pedro Roig, Laia | Lange, Christian | Bonete, María-José | Soppa, Jörg | Maupin-Furlow, Julie
Research Group/s: Biotecnología de Extremófilos (BIOTECEXTREM)
Center, Department or Service: Universidad de Alicante. Departamento de Agroquímica y Bioquímica
Keywords: Archaea | Haloferax | Halophilic | Membrane | Metabolism
Knowledge Area: Bioquímica y Biología Molecular
Issue Date: 28-Aug-2013
Publisher: John Wiley & Sons Ltd.
Citation: MicrobiologyOpen. 2013, 2(5): 826-840. doi:10.1002/mbo3.120
Abstract: Gene homologs of GlnK PII regulators and AmtB-type ammonium transporters are often paired on prokaryotic genomes, suggesting these proteins share an ancient functional relationship. Here, we demonstrate for the first time in Archaea that GlnK associates with AmtB in membrane fractions after ammonium shock, thus, providing a further insight into GlnK-AmtB as an ancient nitrogen sensor pair. For this work, Haloferax mediterranei was advanced for study through the generation of a pyrE2-based counterselection system that was used for targeted gene deletion and expression of Flag-tagged proteins from their native promoters. AmtB1-Flag was detected in membrane fractions of cells grown on nitrate and was found to coimmunoprecipitate with GlnK after ammonium shock. Thus, in analogy to bacteria, the archaeal GlnK PII may block the AmtB1 ammonium transporter under nitrogen-rich conditions. In addition to this regulated protein–protein interaction, the archaeal amtB-glnK gene pairs were found to be highly regulated by nitrogen availability with transcript levels high under conditions of nitrogen limitation and low during nitrogen excess. While transcript levels of glnK-amtB are similarly regulated by nitrogen availability in bacteria, transcriptional regulators of the bacterial glnK promoter including activation by the two-component signal transduction proteins NtrC (GlnG, NRI) and NtrB (GlnL, NRII) and sigma factor σN (σ54) are not conserved in archaea suggesting a novel mechanism of transcriptional control.
Sponsor: This work was supported by project BIO2008-00082 from the Spanish Ministry of Science and Innovation MICINN awarded to MBP, which includes funding from the European Union (“FEDER”). During this work, L. P.-R. was supported by a fellowship (AP2007-02932) from the Spanish Ministry of Education. This work was also funded by project NIH R01 GM057498 from the National Institute of General Medical Science awarded to J. M.-F. and by project DOE DE-FG02-05ER15650 from the Chemical Sciences, Geosciences, and Biosciences Division of the Office of Basic Energy Sciences (BES) in the U.S. Department of Energy (DOE) awarded to J. M.-F.
ISSN: 2045-8827
DOI: 10.1002/mbo3.120
Language: eng
Type: info:eu-repo/semantics/article
Rights: © 2013 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Peer Review: si
Publisher version:
Appears in Collections:INV - BIOTECEXTREM - Artículos de Revistas

Files in This Item:
Files in This Item:
File Description SizeFormat 
Thumbnail2013_Pedro-Roig_etal_MicrobiologyOpen.pdf961,16 kBAdobe PDFOpen Preview

This item is licensed under a Creative Commons License Creative Commons