Biochemical Characterization of Putative Adenylate Dimethylallyltransferase and Cytokinin Dehydrogenase from Nostoc sp. PCC 7120
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26376297
PubMed Central
PMC4574047
DOI
10.1371/journal.pone.0138468
PII: PONE-D-15-20826
Knihovny.cz E-zdroje
- MeSH
- biologická evoluce MeSH
- cytokininy metabolismus MeSH
- Escherichia coli enzymologie růst a vývoj MeSH
- fylogeneze MeSH
- geneticky modifikované rostliny genetika růst a vývoj metabolismus MeSH
- molekulární sekvence - údaje MeSH
- mutace genetika MeSH
- mutageneze cílená MeSH
- Nostoc enzymologie genetika MeSH
- oxidoreduktasy genetika metabolismus MeSH
- prenyltransferáza genetika metabolismus MeSH
- regulace genové exprese enzymů MeSH
- rekombinantní proteiny metabolismus MeSH
- sekvence aminokyselin MeSH
- sekvenční homologie aminokyselin MeSH
- tabák enzymologie růst a vývoj MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- cytokinin oxidase MeSH Prohlížeč
- cytokininy MeSH
- oxidoreduktasy MeSH
- prenyltransferáza MeSH
- rekombinantní proteiny MeSH
Cytokinins, a class of phytohormones, are adenine derivatives common to many different organisms. In plants, these play a crucial role as regulators of plant development and the reaction to abiotic and biotic stress. Key enzymes in the cytokinin synthesis and degradation in modern land plants are the isopentyl transferases and the cytokinin dehydrogenases, respectively. Their encoding genes have been probably introduced into the plant lineage during the primary endosymbiosis. To shed light on the evolution of these proteins, the genes homologous to plant adenylate isopentenyl transferase and cytokinin dehydrogenase were amplified from the genomic DNA of cyanobacterium Nostoc sp. PCC 7120 and expressed in Escherichia coli. The putative isopentenyl transferase was shown to be functional in a biochemical assay. In contrast, no enzymatic activity was detected for the putative cytokinin dehydrogenase, even though the principal domains necessary for its function are present. Several mutant variants, in which conserved amino acids in land plant cytokinin dehydrogenases had been restored, were inactive. A combination of experimental data with phylogenetic analysis indicates that adenylate-type isopentenyl transferases might have evolved several times independently. While the Nostoc genome contains a gene coding for protein with characteristics of cytokinin dehydrogenase, the organism is not able to break down cytokinins in the way shown for land plants.
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