Objectif EXPRESSION OF LIPOXYGENASE GENE IN BAKER YEAST IS EXPECTED TO BLEACH THE YELLOW PIGMENTS OF THE WHEAT FLOUR TO GIVE A BREAD WITH VERY WHITE CRUMB, SIMULTANEOUSLY IMPROVING THE MIXING PROPERTIES OF THE DOUGH INGREDIENTS AND THE STRENGH OF THE DOUGH. THE CONSTRUCTED YEAST STRAINS WILL ALLOW TO TEST THE CORRECTNESS OF THE CURRENT HYPOTHESES AS TO HOW LIPOXYGENASES FROM ADDED SOYA FLOUR INFLUENCE THE CHARACTERISTICS OF THE DOUGH. BY USING STRAINS SECRETING DIFFERENT AMOUNTS OF LIPOXYGENASE, AN ASSESSMENT WILL BE MADE OF THE FLAVOUR CONTRIBUTIONS CAUSED BY THE LIPOXYGENASE CATALYSED PROCESSES AGAINST THOSE ORIGINATING FROM OTHER INGREDIENTS OF ADDED SOYA FLOUR. Integration vectors containing a pea lipoxygenase complementary deoxyribonucleic acid (cDNA) clone have been constructed and industrial yeast strains transformed with these vectors. Intracellular lipoxygenase activity was detectable in some of the transformed cell lines, but no export of the enzyme could be demonstrated.A genetically engineered baker's yeast that produces and secretes legume lipoxygenase could prove valuable in breadmaking. Spore clones of an outstanding industrial strain of baker's yeast have been characterized by tetrad analysis, molecular hybridization with cloned genes and by pulse field gel electrophoresis of chromosomes. Full length complementary deoxyribonucleic acid (cDNA) corresponding to the 2 major pea seed lipoxygenase polypeptides have been isolated, sequenced and shown to direct the transcription of functional beta (mRNA). Vectors for the expression and secretion of the pea lipoxygenase in yeast have been constructed and a plate assay to recognize lipoxygenase producing yeast colonies has been established.An outstanding industrial strain has been characterized; all genes tested to date seem to be organized in the same linkage relationships as in standard academic yeast strains.Near full length cDNA clones of the mRNAs corresponding to the 2 major pea seed lipoxygenases were isolated, sequenced and used in an in vitro transcription translation reaction to demonstrate their potential to produce lipoxygenase in a heterologous situation.Transformation systems were developed to introduce and integrate into the chromosomes of the production strain the cDNAs encoding the pea seed lipoxygenases. Using reporter genes encoding mouse alpha amylase and bacterial beta galactosidase, stable transformants with good expression and secretion were obtained. No enzyme export could be achieved. However with the lipoxygenase clones (so another system based on a successful yeast) an Escherichia coli shuttle vector is being evaluated. A plate assay designed to recognize lipoxygenase producing yeast clones has also been established.THE AIM IS TO CONSTRUCT BY GENETIC ENGINEERING YEAST STRAINS WHICH DURING THE PRODUCTION OF DOUGH SECRETE LIPOXYGENASE FROM AN HETEROLOGOUS CLONED PLANT GENE. STEPS: 1-ISOLATION OF A CDNA CLONE FOR LIPOXYGENASE FROM A PEA SEED MRNA. 2-ISOLATION OF THE SEVERAL GENOMIC LIPOXYGENASE GENES FROM A PEA. 3- SEQUENCE OF THE PLANT LIPOXYGENASE GENES. 4- SELECTION OF AN APPROPRIATE INDUSTRIAL YEAST STRAIN AS A HOST FOR CLONING. 5- TRANSFORMATION BY INTEGRATION USING THE EXPRESSION VECTOR PMS12 CONTAINING THE GENE FOR A AMYLASE WHICH IS SECRETED BY YEAST. 6- SUBSTITUTION OF THE A-AMYLASE GENE BY THE PLANT LIPOXYGENASE GENE. Champ scientifique natural sciencesbiological sciencesgeneticsDNAnatural scienceschemical scienceselectrochemistryelectrophoresisnatural sciencesbiological sciencesgeneticschromosomesnatural sciencesbiological sciencesbiochemistrybiomoleculesproteinsenzymesagricultural sciencesagriculture, forestry, and fisheriesagriculturegrains and oilseedslegumes Programme(s) FP1-BAP - Multiannual research action programme (EEC) in the field of biotechnology (BAP), 1985-1989 Thème(s) Data not available Appel à propositions Data not available Régime de financement CSC - Cost-sharing contracts Coordinateur DANISH DISTILLERIES LTD Contribution de l’UE Aucune donnée Adresse RAFFINADERIVEJ 10 2300 KOEBENHAVN Danemark Voir sur la carte Coût total Aucune donnée Participants (2) Trier par ordre alphabétique Trier par contribution de l’UE Tout développer Tout réduire CARSLBERG LABORATORY Danemark Contribution de l’UE Aucune donnée Adresse COPENHAGEN Voir sur la carte Coût total Aucune donnée JOHN INNES CENTRE Royaume-Uni Contribution de l’UE Aucune donnée Adresse Norwich Research Park, Colney NORWICH Voir sur la carte Liens Site web Opens in new window Coût total Aucune donnée