Unknown

Dataset Information

0

Cloning, expression, crystallization and preliminary X-ray analysis of the XMT and DXMT N-methyltransferases from Coffea canephora (robusta).


ABSTRACT: Caffeine is a secondary metabolite produced by a variety of plants including Coffea canephora (robusta) and there is growing evidence that caffeine is part of a chemical defence strategy protecting young leaves and seeds from potential predators. The genes encoding XMT and DXMT, the enzymes from Coffea canephora (robusta) that catalyse the three independent N-methyl transfer reactions in the caffeine-biosynthesis pathway, have been cloned and the proteins have been expressed in Escherichia coli. Both proteins have been crystallized in the presence of the demethylated cofactor S-adenosyl-L-cysteine (SAH) and substrate (xanthosine for XMT and theobromine for DXMT). The crystals are orthorhombic, with space group P2(1)2(1)2(1) for XMT and C222(1) for DXMT. X-ray diffraction to 2.8 A for XMT and to 2.5 A for DXMT have been collected on beamline ID23-1 at the ESRF.

SUBMITTER: McCarthy AA 

PROVIDER: S-EPMC2330209 | biostudies-literature | 2007 Apr

REPOSITORIES: biostudies-literature

altmetric image

Publications

Cloning, expression, crystallization and preliminary X-ray analysis of the XMT and DXMT N-methyltransferases from Coffea canephora (robusta).

McCarthy Andrew A AA   Biget Laurent L   Lin Chenwei C   Petiard Vincent V   Tanksley Steve D SD   McCarthy James G JG  

Acta crystallographica. Section F, Structural biology and crystallization communications 20070312 Pt 4


Caffeine is a secondary metabolite produced by a variety of plants including Coffea canephora (robusta) and there is growing evidence that caffeine is part of a chemical defence strategy protecting young leaves and seeds from potential predators. The genes encoding XMT and DXMT, the enzymes from Coffea canephora (robusta) that catalyse the three independent N-methyl transfer reactions in the caffeine-biosynthesis pathway, have been cloned and the proteins have been expressed in Escherichia coli.  ...[more]

Similar Datasets

| S-EPMC4282694 | biostudies-literature
| S-EPMC3388932 | biostudies-literature
| S-EPMC3818038 | biostudies-literature
| S-EPMC2795598 | biostudies-literature
| S-EPMC3943092 | biostudies-literature
| S-EPMC2374240 | biostudies-literature
| S-EPMC2664774 | biostudies-literature
| S-EPMC2335007 | biostudies-literature
| S-EPMC8953325 | biostudies-literature
| S-EPMC3509990 | biostudies-literature