| Literature DB >> 33539931 |
Daniela Torres1, Elías Mongiardini2, Florencia Donadío3, Raúl Donoso4, Gonzalo Recabarren-Gajardo5, José Gualpa6, Stijn Spaepen7, Roberto Defez8, Gastón Lopez9, Carmen Bianco10, Fabricio Cassán11.
Abstract
Bradyrhizobium japonicum E109 is a bacterium widely used for inoculants production in Argentina. It is known for its ability to produce several phytohormones and degrade indole-3-acetic acid (IAA). The genome sequence of B. japonicum E109 was recently analyzed and it showed the presence of genes related to the synthesis of IAA by indole-3-acetonitrile, indole-3-acetamide and tryptamine pathways. Nevertheless, B. japonicum E109 is not able to produce IAA and instead has the ability to degrade this hormone under saprophytic culture conditions. This work aimed to study the molecular and physiological features of IAA degradation and identify the genes responsible of this activity. In B. japonicum E109 we identified two sequences coding for a putative 3-phenylpropionate dioxygenase (subunits α and β) responsible for the IAA degradation that were homologous to the canonical cluster of iacC and iacD of Pseudomonas putida 1290. These genes form a separate cluster together with three additional genes with unknown functions. The degradation activity was found to be constitutively expressed in B. japonicum E109. As products of IAA degradation, we identified two compounds, 3-indoleacetic acid 2,3-oxide and 2-(2-hydroperoxy-3-hydroxyindolin-3-yl) acetic acid. Our report proposes, for the first time, a model for IAA degradation in Bradyrhizobium.Entities:
Keywords: 2-(2-Hydroperoxy-3-hydroxyindolin-3-yl) acetic acid; 3-Indoleacetic acid 2; 3-Oxide; 3-Phenylpropionate dioxygenase; B. japonicum; Indole-3-acetic acid
Year: 2021 PMID: 33539931 DOI: 10.1016/j.resmic.2021.103814
Source DB: PubMed Journal: Res Microbiol ISSN: 0923-2508 Impact factor: 3.992