Search results for "Heterologous expression."

showing 8 items of 48 documents

Study of biogenic amines metabolism in wine lactic acid bacteria

2011

Biogenic amines are indesirable compounds found in fermented products like wine. Lactic acid bacteria from wine, including Oenococcus oeni, the main actor of malolactic fermentation, are able to produce these molecules from nitrogenous precursors. In order to limited biogenic amines accumulation, it is necessary to understand the role of this production by strains responsible for the synthesis of these metabolites in food. That is why the European BiamFood project was put in place. Along my thesis, molecular tools were developed in order to mutate O. oeni genes (encoding decarboxylases), and to express genes of interest. Genetic clusters hdc from L. higardii and odc from O. oeni, responsibl…

[SDV.SA] Life Sciences [q-bio]/Agricultural sciencesBiogenic aminesAmines biogènes[ SDV.AEN ] Life Sciences [q-bio]/Food and NutritionWine[SDV.AEN] Life Sciences [q-bio]/Food and NutritionBactéries lactiquesSuicide vectorsVinLactic acid bacteriaVecteurs suicidesExpression hétérologueHeterologous expressionOenococcus oeniPeptides[ SDV.SA ] Life Sciences [q-bio]/Agricultural sciences
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Magnaporthe oryzae as an expression host for the production of the unspecific peroxygenase AaeUPO from the basidiomycete Agrocybe aegerita.

2021

Abstract The filamentous fungus Magnaporthe oryzae has the potential to be developed as an alternative platform organism for the heterologous production of industrially important enzymes. M. oryzae is easy to handle, fast‐growing and unlike yeast, posttranslational modifications like N‐glycosylations are similar to the human organism. Here, we established M. oryzae as a host for the expression of the unspecific peroxygenase from the basidiomycete Agrocybe aegerita (AaeUPO). Note, UPOs are attractive biocatalysts for selective oxyfunctionalization of non‐activated carbon‐hydrogen bonds. To improve and simplify the isolation of AaeUPO in M. oryzae, we fused a Magnaporthe signal peptide for pr…

biologyAgrocybeHost (biology)Eukaryotic Initiation Factor-1heterologous expressionfood and beveragesMagnaporthe oryzaeProtein Sorting Signalsbiology.organism_classificationMicrobiologyQR1-502Recombinant ProteinsMicrobiologyMixed Function OxygenasesAaeUPOoxyfunctionalizationFungal ProteinsMagnaporthe oryzaeMagnaportheunspecific peroxygenasesUnspecific peroxygenaseCommentaryAgrocybeHeterologous expressionPromoter Regions GeneticMicrobiologyOpen
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Biochemical characterization of two functional human liver acyl-CoA oxidase isoforms 1a and 1b encoded by a single gene

2007

Abstract Human acyl-CoA oxidase 1 (ACOX1) is a rate-limiting enzyme in peroxisomal fatty acids β-oxidation and its deficiency is associated with a lethal, autosomal recessive disease, called pseudoneonatal-adrenoleukodystrophy. Two mRNA variants, transcribed from a single gene encode ACOX1a or ACOX1b isoforms, respectively. Recently, a mutation in a splice site has been reported [H. Rosewich, H.R. Waterham, R.J. Wanders, S. Ferdinandusse, M. Henneke, D. Hunneman, J. Gartner, Pitfall in metabolic screening in a patient with fatal peroxisomal β-oxidation defect, Neuropediatrics 37 (2006) 95–98.], which results in the defective peroxisomal fatty acids β-oxidation. Here, we show that these mRNA…

chemistry.chemical_classificationGene isoformOxidase testBiophysicsCell BiologyBiologyPeroxisomeBiochemistryIsozymeMolecular biologyArticleEnzyme ActivationIsoenzymesMolecular WeightEnzymechemistryBiochemistryLiverEnzyme StabilityAcyl-CoA oxidaseACOX1HumansHeterologous expressionAcyl-CoA OxidaseMolecular Biology
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Production of soluble eukaryotic recombinant proteins in E. coli is favoured in early log-phase cultures induced at low temperature

2013

Abstract Background Producing recombinant plant proteins expressed in Escherichia coli produce in high yields and in a soluble and functional form can be difficult. Under overexpression conditions, proteins frequently accumulate as insoluble aggregates (inclusion bodies) within the producing bacteria. We evaluated how the initial culture density, temperature and duration of the expression stage affect the production of some eukaryotic enzymes in E. coli. Findings A high yield of active soluble proteins was obtained by combining early-log phase cultures and low temperatures for protein induction. When IPTG was added at OD600 = 0.1 and cultures were maintained at 4°C for 48-72 h, the soluble …

chemistry.chemical_classificationMultidisciplinarybusiness.industryShort Reportlac operonBiologymedicine.disease_causeFunctional proteinsInclusion bodiesBiotechnologylaw.inventionEnzymeBiochemistrychemistrylawProtein purificationmedicineRecombinant DNALow temperatureSoluble recombinant proteinsTarget proteinHeterologous expressionbusinessEscherichia coliEarly log phaseSpringerPlus
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The gene encoding polyneuridine aldehyde esterase of monoterpenoid indole alkaloid biosynthesis in plants is an ortholog of theα/β hydrolase super fa…

2000

The biosynthesis of the anti-arrhythmic alkaloid ajmaline is catalysed by more than 10 specific enzymes. In this multistep process polyneuridine aldehyde esterase (PNAE) catalyses a central reaction by transforming polyneuridine aldehyde into epi-vellosimine, which is the immediate precursor for the synthesis of the ajmalane skeleton. PNAE was purified from cell suspension cultures of Rauvolfia serpentina. The N-terminal sequence and endoproteinase LysC fragments of the purified protein were used for primer design and for the amplification of specific PCR products leading to the isolation of PNAE-encoding cDNA from a R. serpentina library. The PNAE cDNA was fused with a C-terminal His-tag, …

chemistry.chemical_classificationbiologyStereochemistrymedicine.disease_causebiology.organism_classificationBiochemistryPolyneuridine-aldehyde esterasechemistry.chemical_compoundEnzymeBiosynthesischemistryBiochemistryRauvolfia serpentinaComplementary DNAHydrolasemedicineHeterologous expressionEscherichia coliEuropean Journal of Biochemistry
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(2S,3S)-2-Azaniumyl-4-[(1S,4aS,4bS,6S,7S,8aS,10aS)-6,7-dihydroxy-2,4b,8,8,10a-pentamethyl-1,4,4a,4b,5,6,7,8,8a,9,10,10a-dodecahydrophenanthren-1-yl]-…

2018

The title compound, which crystallized as a methanol and water solvate, C24H41NO5·CH4O·H2O, was obtained by heterologous expression of the brasilicardin gene cluster in the bacterium Amycolatopsis japonicum. In the crystal, the components are linked by numerous hydrogen bonds, generating a three-dimensional network.

crystal structureperhydrophenanthrenelcsh:QD901-999heterologous expressionlcsh:CrystallographyBrasilicardin AIUCrData
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Expression, purification, crystallization and preliminary X-ray analysis of perakine reductase, a new member of the aldo-keto reductase enzyme superf…

2006

Perakine reductase (PR) is a novel member of the aldo-keto reductase enzyme superfamily from higher plants. PR from the plant Rauvolfia serpentina is involved in the biosynthesis of monoterpenoid indole alkaloids by performing NADPH-dependent reduction of perakine, yielding raucaffrinoline. However, PR can also reduce cinnamic aldehyde and some of its derivatives. After heterologous expression of a triple mutant of PR in Escherichia coli, crystals of the purified and methylated enzyme were obtained by the hanging-drop vapour-diffusion technique at 293 K with 100 mM sodium citrate pH 5.6 and 27% PEG 4000 as precipitant. Crystals belong to space group C222(1) and diffract to 2.0 A, with unit-…

endocrine systemStereochemistryAldo-Keto ReductasesBiophysicsAlcohol oxidoreductaseReductaseCrystallography X-Raymedicine.disease_causeBiochemistryRauwolfiachemistry.chemical_compoundBiosynthesisAldehyde ReductaseStructural BiologyRauvolfia serpentinaGeneticsmedicineEscherichia colichemistry.chemical_classificationAldo-keto reductasebiologyCondensed Matter Physicsbiology.organism_classificationAlcohol OxidoreductasesEnzymeBiochemistrychemistryCrystallization CommunicationsHeterologous expressionCrystallizationActa Crystallographica Section F Structural Biology and Crystallization Communications
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External Versus Internal Metabolic Activation of Polycyclic Aromatic Compounds in Mutagenicity Tests: A Comparison Using Heterologous Expression Syst…

1996

Abstract Benzo[a]pyrene-trans-7,8-dihydrodiol was virtually non-mutagenic to Chinese hamster V79p cells, but was strongly mutagenic to a V79-derived cell line expressing cytochrome P450 1A1, when the cells were exposed separately. In mixed cultures of these two cell types, it showed about 50 % of the mutagenic activity in V79p cells, compared to that observed in the enzyme-proficient cell line, indicating an efficient intercellular transfer of the active metabolite. The benzylic alcohols 1-hydroxymethylpyrene and 6-hydroxymethylbenzo[a]-pyrene were weakly mutagenic to Salmonella typhimurium TA1538 in the absence of a metabolic activation system, but were potent mutagens to a TA1538-derived …

endocrine systemSulfotransferasePolymers and PlasticsbiologyChemistryfungiOrganic Chemistryfood and beveragesCytochrome P450biology.organism_classificationChinese hamsterchemistry.chemical_compoundCytosolBiochemistryCell cultureMaterials Chemistrybiology.proteinPyreneHeterologous expressionHydroxysteroidPolycyclic Aromatic Compounds
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