Search results for "Auxotrophy"

showing 10 items of 13 documents

On the fermentative behavior of auxotrophic strains of Saccharomyces cerevisiae

2014

Background: The selection of new yeast strains could lead to improvements in bioethanol production. Here, we have studied the fermentative capacity of different auxotrophic mutants of Saccharomyces cerevisiae, which are routinely used as hosts for the production of heterologous proteins. It has recently been found that these strains exhibit physiological alterations and peculiar sensitivities with respect to the parental prototrophic strains from which they derive. In this work the performance of auxotrophic S. cerevisiae CEN.PK strains was compared to the corresponding prototrophic strain, to S. cerevisiae T5bV, a strain isolated from grape must and to another auxotrophic strain, S. cerevi…

biologyStrain (chemistry)Fermentative capacitylcsh:BiotechnologyAuxotrophySaccharomyces cerevisiaeFermentative metabolismHeterologousAuxotrophic yeastbiology.organism_classificationApplied Microbiology and BiotechnologyYeastEthanol yieldslcsh:Biology (General)Biochemistrylcsh:TP248.13-248.65Ethanol yieldEthanol fuelFermentationCEN.PK strainsAuxotrophic yeast; CEN.PK strains; Ethanol yields; Fermentative capacity; Fermentative metabolismlcsh:QH301-705.5BiotechnologyElectronic Journal of Biotechnology
researchProduct

Yeast vectors for the integration/expression of any sequence at theTYR1 locus

2007

We have constructed new yeast vectors for targeted integration and conditional expression of any sequence at the Saccharomyces cerevisiae TYR1 locus which becomes disrupted. We show that vector integration is not neutral, causing prototrophy for tyrosine and auxotrophy for the vector's selectable marker (uracil or leucine, depending on the vector used). This feature allows a double screening of transformed yeast cells, improving the identification of colonies with the desired chromosomal structure. The GAL10 gene promoter has been added to drive conditional expression of cloned sequences. Using these vectors, chromosomal structure verification of recombinant clones is no longer necessary, s…

Sequence analysisAuxotrophyGenetic VectorsGreen Fluorescent ProteinsMolecular Sequence DataSaccharomyces cerevisiaeBioengineeringLocus (genetics)Saccharomyces cerevisiaeBiologyPolymerase Chain ReactionApplied Microbiology and BiotechnologyBiochemistryGenes ReporterGene Expression Regulation FungalGeneticsDNA FungalSelectable markerRegulation of gene expressionGeneticsExpression vectorBase SequenceSequence Analysis DNAbiology.organism_classificationMutagenesis InsertionalTyrosineHeterologous expressionBiotechnologyYeast
researchProduct

Penicillium auxotrophic mutants can be detected by suing xanthene dyes

1987

Auxotrophic mutants ofPenicillium spp. have been directly isolated after mutagenic treatment from agar plates containing Xanthene dyes. They grow as characteristic small colored colonies. Some strains were tested and they showed a differential response depending on the Xanthene dye used.

PharmacologyXanthenebiologyAuxotrophyMutagenesis (molecular biology technique)Cell BiologyFungi imperfectibiology.organism_classificationAgar plateCellular and Molecular Neurosciencechemistry.chemical_compoundchemistryBiochemistryXanthene dyePenicilliumAuxotrophic mutantMolecular MedicineMolecular BiologyExperientia
researchProduct

Global effects of ade8 deletion on budding yeast metabolism

2021

AbstractPurine auxotrophy is a typical marker for many laboratory yeast strains. Supplementation of additional purine source (like adenine) is necessary to cultivate these strains. If not supplied in adequate amounts, purine starvation sets in. We tested purine starvation effects in budding yeast Saccharomyces cerevisiae ade8 knockout. We explored effects brought by purine starvation in cellular, central carbon metabolism and in the global transcriptome level.We observed that cells cultivated in purine depleted media became significantly more tolerant to severe thermal, oxidative and desiccation stresses when compared to the cells cultivated in media with all necessary supplements. When sta…

Purinechemistry.chemical_compoundbiologyChemistryAuxotrophySaccharomyces cerevisiaeAdenylate kinaseRNAbiology.organism_classificationPurine metabolismYeastIntracellularCell biology
researchProduct

FLYCOP: metabolic modeling-based analysis and engineering microbial communities

2018

10 p.-5 fig.-2 tab.

0301 basic medicineStatistics and ProbabilityComputer scienceMetaboliteAuxotrophy030106 microbiologyMicrobial ConsortiaEccb 2018: European Conference on Computational Biology ProceedingsEvolutionary engineeringmedicine.disease_causeBiochemistry03 medical and health scienceschemistry.chemical_compoundmedicineEscherichia coliMetabolic modelingMolecular BiologyEscherichia coli2. Zero hungerbiologyMicrobiotaSystemsBiological evolutionSynechococcusbiology.organism_classificationComputer Science ApplicationsComputational MathematicsMulticellular organism030104 developmental biologyComputational Theory and MathematicschemistryMetabolic EngineeringBiochemical engineeringSoftwareBioinformatics
researchProduct

Selenomethionine labeling of large biological macromolecular complexes: probing the structure of marine bacterial virus PM2.

2008

There is a need for improved tools for labeling protein species within large macromolecular assemblies. Here we describe a method for the efficient selenomethionine labeling of the membrane-containing bacterial virus PM2 for structural studies. By examining potential host cells a strain was found which was auxotrophic for methionine, and by performing a multiparameter search of conditions it was possible to derive a robust protocol which simultaneously minimized the toxic effects of the selenomethionine, so that a reasonable virus yield was maintained, whilst still achieving essentially complete labeling. This has allowed us to fingerprint the protein constituents of the virus in a relative…

0303 health sciencesbiologyStrain (chemistry)030306 microbiologyAuxotrophyCorticoviridaechemistry.chemical_elementCrystallography X-Raybiology.organism_classificationVirusBacteriophage03 medical and health scienceschemistryBiochemistryStructural BiologyYield (chemistry)MethodsBacterial virusSelenomethionineSelenium030304 developmental biologyMacromoleculeJournal of structural biology
researchProduct

Amino acids role in biogenic amine production by Oenococcus Oeni

2013

In wine biogenic amines (BA) are mainly of microbial origin, Oenococcus oeni, the mainresponsible for malolactic fermentation, has been identified as a BA producer from nitrogenprecursors. Oenococcus oeni possess numerous amino acid auxotrophies that are precursors ofbiogenic amines. No study has been done so far to look at the relationship betweenauxotrophy for amino acids precursors of BA and the level of BA in the medium. In order todo so, 80 Oenococcus oeni strains were isolated from red wines. The detection of genesencoding the different decarboxylases responsible for BA synthesis has been realised. Inparallel, the auxotrophy for the four amino acids (Arg, Tyr, His, Phe) precursors of …

[SDV.SA]Life Sciences [q-bio]/Agricultural sciences[SDV.SA] Life Sciences [q-bio]/Agricultural sciencesAgmatineWineAuxotrophie[SHS.ECO]Humanities and Social Sciences/Economics and FinanceAuxotrophy[CHIM.OTHE] Chemical Sciences/Other[ CHIM.OTHE ] Chemical Sciences/OtherVinAmine production[ SHS.ECO ] Humanities and Social Sciences/Economies and finances[SHS.ECO] Humanities and Social Sciences/Economics and Finance[CHIM.OTHE]Chemical Sciences/OtherOenococcus oeni[ SDV.SA ] Life Sciences [q-bio]/Agricultural sciences
researchProduct

Propyldazine is mutagenic inSalmonella typhimurium and Escherichia coli: Distinct specificity for strains TA1537 AND TA97

1985

The antihypertensive drug propyldazine (Atensil) was demonstrated to be muta- genic with auxotrophic mutants of Salmonella typhimurium and Escherichia coli. Addition of liver S9 mix (postmitochondrial supernatant fraction supplemented with an NADPH-generating system) had little, if any, effect on the mutagenicity. The mutagenicity showed an unusual pattern of strain specificity. Increased fre- quencies of reversion were observed with all strains whose auxotrophy was caused by frame-shift mutations: the number of revertant colonies per plate from S. typhimurium TA98, TA1538, TA97, and TA1537 was increased up to 5-, 9-, 43-, and 160-fold, respectively, above background. Among the strains that…

MaleSalmonella typhimuriumSalmonellaHealth Toxicology and MutagenesisAuxotrophyReversionMutagenBiologyToxicologymedicine.disease_causeAmes testMicrobiologySpecies SpecificityEscherichia coliGeneticsmedicineAnimalsEscherichia coliBiotransformationGenetics (clinical)DihydralazineStrain (chemistry)Mutagenicity Testsfood and beveragesRats Inbred StrainsHydralazineDihydralazineRatsPyridazinesOncologyMutationMicrosomes LiverMutagensmedicine.drugTeratogenesis, Carcinogenesis, and Mutagenesis
researchProduct

Adenine auxotrophy--be aware: some effects of adenine auxotrophy in Saccharomyces cerevisiae strain W303-1A.

2013

Adenine auxotrophy is a commonly used genetic marker in haploid yeast strains. Strain W303-1A, which carries the ade2-1 mutation, is widely used in physiological and genetic research. Yeast extract-based rich medium contains a low level of adenine, so that adenine is often depleted before glucose. This could affect the cell physiology of adenine auxotrophs grown in rich medium. The aim of our study was to assess the effects of adenine auxotrophy on cell morphology and stress physiology. Our results show that adenine depletion halts cell division, but that culture optical density continues to increase due to cell swelling. Accumulation of trehalose and a coincident 10-fold increase in desicc…

Cell physiologyCell divisionAuxotrophyAdenineSaccharomyces cerevisiaeGeneral MedicineSaccharomyces cerevisiaeBiologybiology.organism_classificationCell morphologyApplied Microbiology and BiotechnologyMicrobiologyTrehaloseYeastCulture Mediachemistry.chemical_compoundBiochemistrychemistryStress PhysiologicalBiomassLeucineCell DivisionFEMS yeast research
researchProduct

Purine auxotrophy: Possible applications beyond genetic marker

2019

Exploring new drug candidates or drug targets against many illnesses is necessary as "traditional" treatments lose their effectivity. Cancer and sicknesses caused by protozoan parasites are among these diseases. Cell purine metabolism is an important drug target. Theoretically, inhibiting purine metabolism could stop the proliferation of unwanted cells. Purine metabolism is similar across all eukaryotes. However, some medically important organisms or cell lines rely on their host purine metabolism. Protozoans causing malaria, leishmaniasis, or toxoplasmosis are purine auxotrophs. Some cancer forms have also lost the ability to synthesize purines de novo. Budding yeast can serve as an effect…

0106 biological sciencesPurineAuxotrophySaccharomyces cerevisiaeBioengineeringSaccharomyces cerevisiaeBiology01 natural sciencesApplied Microbiology and BiotechnologyBiochemistry03 medical and health scienceschemistry.chemical_compoundDrug DevelopmentNeoplasms010608 biotechnologyGeneticsHumansPurine metabolism030304 developmental biology0303 health sciencesAdenineEukaryotaCell Cycle CheckpointsMetabolismCell cyclebiology.organism_classificationYeastchemistryBiochemistryPurinesCancer cellBiotechnologyYeast
researchProduct