Affinity chromatography reveals RuBisCO as an ecdysteroid-binding protein
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
18761365
DOI
10.1016/j.steroids.2008.07.009
PII: S0039-128X(08)00211-0
Knihovny.cz E-zdroje
- MeSH
- chromatografie afinitní * MeSH
- cytosol enzymologie MeSH
- ekdysteron metabolismus MeSH
- enzymy imobilizované MeSH
- ribulosa-1,5-bisfosfát-karboxylasa izolace a purifikace metabolismus MeSH
- Spinacia oleracea enzymologie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- ekdysteron MeSH
- enzymy imobilizované MeSH
- ribulosa-1,5-bisfosfát-karboxylasa MeSH
The aim of this work was to isolate plant ecdysteroid-binding proteins using affinity chromatography. Ecdysteroids as insect hormones have been investigated thoroughly but their function and the mechanism of action in plants and other organisms is still unknown although ecdysteroids occur in some plants in a relatively large amount. Therefore, 20-hydroxyecdysone was immobilized on a polymeric carrier as a ligand for affinity chromatography in order to isolate plant ecdysteroid-binding proteins from the cytosolic extract of New Zealand spinach (Tetragonia tetragonoides). Non-specifically bound proteins were eluted with a rising gradient of concentration of sodium chloride, and 3% (v/v) acetic acid was used for the elution of the specifically bound proteins. Using this method, ribulose 1,5-bisphosphate carboxylase/oxygenase (RuBisCO) was isolated. The influence of ecdysteroids on RuBisCO was further studied. Our results show that ecdysteroids are able to increase the yield of RuBisCO-mediated reaction in which CO(2) is fixed into organic matter by more than 10%.
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