New NodW- or NifA-Regulated Bradyrhizobium japonicum Genes

A cluster of genes coding for putative plant cell-wall degrading enzymes (i.e., genes for two endoglucanases [gunA and gunA2], one pectinmethylesterase [pme], and one polygalacturonase [pgl]) was identified by sequence similarities in the symbiotic region of the Bradyrhizobium japonicum chromosome....

Full description

Bibliographic Details
Main Authors: Isabelle Caldelari Baumberger, Nicole Fraefel, Michael Göttfert, Hauke Hennecke
Format: Article
Language:English
Published: The American Phytopathological Society 2003-04-01
Series:Molecular Plant-Microbe Interactions
Subjects:
Online Access:https://apsjournals.apsnet.org/doi/10.1094/MPMI.2003.16.4.342
_version_ 1811291282639683584
author Isabelle Caldelari Baumberger
Nicole Fraefel
Michael Göttfert
Hauke Hennecke
author_facet Isabelle Caldelari Baumberger
Nicole Fraefel
Michael Göttfert
Hauke Hennecke
author_sort Isabelle Caldelari Baumberger
collection DOAJ
description A cluster of genes coding for putative plant cell-wall degrading enzymes (i.e., genes for two endoglucanases [gunA and gunA2], one pectinmethylesterase [pme], and one polygalacturonase [pgl]) was identified by sequence similarities in the symbiotic region of the Bradyrhizobium japonicum chromosome. In addition, a systematic screen of the region revealed several genes potentially transcribed by the σ54-RNA polymerase and activated by the transcriptional regulator NifA (i.e., genes for proteins with similarity to outer membrane proteins [id117 and id525] and a citrate carrier [id331 or citA] and one open reading frame without similarity to known proteins [id747]). Expression studies using transcriptional lacZ fusions showed that gunA2 and pgl were strongly induced by the isoflavone genistein in a NodW-dependent manner, suggesting a role of the gene products in early events of the nodulation process; by contrast, gunA and pme expression was very weak in the conditions tested. The gunA2 gene product was purified and was shown to have cellulase activity. β-Galactosidase activity expressed from transcriptional lacZ fusions to id117, id525, and id747 in the wild type and in nifA and rpoN mutant backgrounds confirmed that their transcription was dependent on NifA and σ54. Despite the presence of a -24/-12-type promoter and a NifA binding site upstream of citA, no regulation could be demonstrated in this case. Null mutations introduced in gunA, gunA2, pgl, pme, citA, id117, id525, and id747 did not impair the symbiosis with the host plants.
first_indexed 2024-04-13T04:27:06Z
format Article
id doaj.art-b1a8df65f38040ed8a08bcbd8c700752
institution Directory Open Access Journal
issn 0894-0282
1943-7706
language English
last_indexed 2024-04-13T04:27:06Z
publishDate 2003-04-01
publisher The American Phytopathological Society
record_format Article
series Molecular Plant-Microbe Interactions
spelling doaj.art-b1a8df65f38040ed8a08bcbd8c7007522022-12-22T03:02:28ZengThe American Phytopathological SocietyMolecular Plant-Microbe Interactions0894-02821943-77062003-04-0116434235110.1094/MPMI.2003.16.4.342New NodW- or NifA-Regulated Bradyrhizobium japonicum GenesIsabelle Caldelari BaumbergerNicole FraefelMichael GöttfertHauke HenneckeA cluster of genes coding for putative plant cell-wall degrading enzymes (i.e., genes for two endoglucanases [gunA and gunA2], one pectinmethylesterase [pme], and one polygalacturonase [pgl]) was identified by sequence similarities in the symbiotic region of the Bradyrhizobium japonicum chromosome. In addition, a systematic screen of the region revealed several genes potentially transcribed by the σ54-RNA polymerase and activated by the transcriptional regulator NifA (i.e., genes for proteins with similarity to outer membrane proteins [id117 and id525] and a citrate carrier [id331 or citA] and one open reading frame without similarity to known proteins [id747]). Expression studies using transcriptional lacZ fusions showed that gunA2 and pgl were strongly induced by the isoflavone genistein in a NodW-dependent manner, suggesting a role of the gene products in early events of the nodulation process; by contrast, gunA and pme expression was very weak in the conditions tested. The gunA2 gene product was purified and was shown to have cellulase activity. β-Galactosidase activity expressed from transcriptional lacZ fusions to id117, id525, and id747 in the wild type and in nifA and rpoN mutant backgrounds confirmed that their transcription was dependent on NifA and σ54. Despite the presence of a -24/-12-type promoter and a NifA binding site upstream of citA, no regulation could be demonstrated in this case. Null mutations introduced in gunA, gunA2, pgl, pme, citA, id117, id525, and id747 did not impair the symbiosis with the host plants.https://apsjournals.apsnet.org/doi/10.1094/MPMI.2003.16.4.342nitrogen fixationnod genes
spellingShingle Isabelle Caldelari Baumberger
Nicole Fraefel
Michael Göttfert
Hauke Hennecke
New NodW- or NifA-Regulated Bradyrhizobium japonicum Genes
Molecular Plant-Microbe Interactions
nitrogen fixation
nod genes
title New NodW- or NifA-Regulated Bradyrhizobium japonicum Genes
title_full New NodW- or NifA-Regulated Bradyrhizobium japonicum Genes
title_fullStr New NodW- or NifA-Regulated Bradyrhizobium japonicum Genes
title_full_unstemmed New NodW- or NifA-Regulated Bradyrhizobium japonicum Genes
title_short New NodW- or NifA-Regulated Bradyrhizobium japonicum Genes
title_sort new nodw or nifa regulated bradyrhizobium japonicum genes
topic nitrogen fixation
nod genes
url https://apsjournals.apsnet.org/doi/10.1094/MPMI.2003.16.4.342
work_keys_str_mv AT isabellecaldelaribaumberger newnodwornifaregulatedbradyrhizobiumjaponicumgenes
AT nicolefraefel newnodwornifaregulatedbradyrhizobiumjaponicumgenes
AT michaelgottfert newnodwornifaregulatedbradyrhizobiumjaponicumgenes
AT haukehennecke newnodwornifaregulatedbradyrhizobiumjaponicumgenes