Search results for "Holoenzymes"

showing 3 items of 3 documents

Glutamine synthetases of green and etiolated leaves ofSinapis alba : Evidence of the identity of the respective enzyme proteins.

1989

Studies on the glutamine synthetases (GS, EC 6.3.1.2) of green (GS2) and etiolated leaves (GSet) ofSinapis alba L. (cv. Steinacher) revealed striking similarities between the respective enzyme proteins. The enzymes showed corresponding chromatographic properties, both on dimethylaminoethyl-Sephacel and on hydroxylapatite columns. The purified GS proteins were also identical with regard to the molecular weight of their subunits. Isoelectrofocusing of pure GSet yielded two distinct polypeptide bands in the pH 5.6 region of the gels. This pattern corresponded to the two strong bands of GS2. Two charge variants of GS polypeptides could be detected by Western-blot analysis of the soluble protein…

Antiserumchemistry.chemical_classificationGel electrophoresisImmunoprecipitationPlant ScienceBiologyGlutamineEnzymeBiochemistrychemistryHoloenzymesGlutamine synthetaseEtiolationGeneticsPlanta
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Differential sensitivity of rat hepatocyte CYP isoforms to self-generated nitric oxide.

2001

AbstractEarly loss of P450 in rat hepatocyte cultures appears directly related to nitric oxide (NO) overproduction. This study investigates the influence of endogenously generated NO (or NO-derived species) on the relative expression of cytochrome P450 (CYP) isoforms in rat hepatocytes. Our results support the view that loss of P450 holoenzyme in culture is the ultimate consequence of a NO driven process, activated during the common hepatocyte isolation procedure, that leads to an accelerated and selective degradation of specific CYP apoproteins. Under conditions in which NO and peroxynitrite formation is operative, changes in the level of specific CYP isoforms result in a significant alter…

Gene isoformMaleTime FactorsBlotting WesternBiophysicsNitric OxideBiochemistryDexamethasoneNitric oxideRats Sprague-Dawleychemistry.chemical_compoundP450 contentApoenzymesCytochrome P-450 Enzyme Systembeta-NaphthoflavoneStructural BiologyGeneticsmedicineAnimalsInducerOverproductionMolecular BiologyCells CulturedDrug metabolismbiologyCytochrome P450Cell BiologyCytochrome P450 inductionCell biologyRatsIsoenzymesmedicine.anatomical_structureNG-Nitroarginine Methyl EsterBiochemistrychemistryHepatocyteEnzyme Inductionbiology.proteinHepatocytesNitric Oxide SynthaseCytochrome P450 isoformRat hepatocyte cultureHoloenzymesPeroxynitriteDrug metabolismFEBS letters
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Modification of the proteolytic fragmentation pattern upon oxidation of cysteines from ribulose 1,5-bisphosphate carboxylase/oxygenase.

2003

The proteolytic susceptibility of the native CO 2 -fixing photosynthetic enzyme ribulose 1,5-bisphosphate carboxylase/oxygenase (EC 4.1.1.39, Rubisco) has been shown to increase in vitro after oxidative treatments that affect cysteine thiols. A limited incubation of oxidized (pretreated with the disulfide cystamine) Rubisco from Chlamydomonas reinhardtii with subtilisin or proteinase K generated fragments of molecular mass about 53 kDa (band I in SDS-PAGE) and 47 kDa (band II) derived from the large subunit (55 kDa) of the enzyme. In contrast, proteolysis of the reduced Rubisco (pretreated with the free thiol cysteamine) produced only the 53 kDa band. The same fragmentation pattern was repr…

OxygenaseProtein subunitRibulose-Bisphosphate CarboxylaseMolecular Sequence DataBiochemistrychemistry.chemical_compoundEndopeptidasesAnimalsEuglena gracilisAmino Acid SequenceCysteineConserved SequenceRibulose 15-bisphosphatebiologyRibuloseHydrolysisfungiRuBisCOSubtilisinPeptide FragmentsKineticsProtein SubunitschemistryBiochemistryModels Chemicalbiology.proteinProtein quaternary structureHoloenzymesOxidation-ReductionProtein Processing Post-TranslationalChlamydomonas reinhardtiiCysteineBiochemistry
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