July
2001
, Volume
14
, Number
7
Pages
823
-
831
Authors
Rosarita
Tatè
,
Luigi
Mandrich
,
Maria R.
Spinosa
,
Anna
Riccio
,
Alessandro
Lamberti
,
Maurizio
Iaccarino
,
and
Eduardo J.
Patriarca
Affiliations
International Institute of Genetics and Biophysics, CNR, Via G. Marconi 10, 80125 Naples, Italy
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RelatedArticle
Accepted 12 March 2001.
Abstract
We show that the protein encoded by the glutamine synthetase translational inhibitor (gstI) gene reduces the NH4+ assimilation capacity of Rhizobium leguminosarum. In this organism, gstI expression is regulated by the ntr system, including the PII 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 N2-fixing SBs. In young SBs, the PII 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 NH4+ metabolism.
JnArticleKeywords
Additional keywords:
histochemical localization,
PCR mutagenesis,
posttranscriptional regulation,
protein purification,
Vicia hirsuta.
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ArticleCopyright
© 2001 The American Phytopathological Society