Open AccessThe Rhizobium GstI Protein Reduces the NH4+ Assimilation Capacity of Rhizobium leguminosarum
Author(s) -
Rosarita Tatè,
Luigi Mandrich,
Maria Rita Spinosa,
Anna Riccio,
Alessandro Lamberti,
Maurizio Iaccarino,
Eduardo J. Patriarca
Publication year - 2001
Publication title -
molecular plant-microbe interactions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.565
H-Index - 153
eISSN - 1943-7706
pISSN - 0894-0282
DOI - 10.1094/mpmi.2001.14.7.823
Subject(s) - glutamine synthetase , rhizobium leguminosarum , rhizobium , biology , glutamine , gene , biochemistry , gene expression , amino acid , rhizobiaceae , symbiosis , bacteria , microbiology and biotechnology , genetics
We show that the protein encoded by the glutamine synthetase translational inhibitor (gstI) gene reduces the NH 4 + assimilation capacity of Rhizobium leguminosarum. In this organism, gstI expression is regulated by the ntr system, including the P II protein, as a function of the nitrogen (N) status of the cells. The GstI protein, when expressed from an inducible promoter, inhibits glutamine synthetase II (glnII) expression under all N conditions tested. The induction of gstI affects the growth of a glutamine synthetase I (glnA - ) strain and a single amino acid substitution (W48D) results in the complete loss of GstI function. During symbiosis, gstI is expressed in young differentiating symbiosomes (SBs) but not in differentiated N 2 -fixing SBs. In young SBs, the P II protein modulates the transcription of NtrC-regulated genes such as gstI and glnII. The evidence presented herein strengthens the idea that the endocytosis of bacteria inside the cytoplasm of the host cells is a key step in the regulation of NH 4 + metabolism.