about
CTP limitation increases expression of CTP synthase in Lactococcus lactisBistability in a metabolic network underpins the de novo evolution of colony switching in Pseudomonas fluorescensScreening of lactic acid bacteria for their potential as microbial cell factories for bioconversion of lignocellulosic feedstocksPhosphoribosyl Diphosphate (PRPP): Biosynthesis, Enzymology, Utilization, and Metabolic Significance.The pyrimidine operon pyrRPB-carA from Lactococcus lactisThe PurR regulon in Lactococcus lactis - transcriptional regulation of the purine nucleotide metabolism and translational machinery.Metabolic characterization and transformation of the non-dairy Lactococcus lactis strain KF147, for production of ethanol from xylose.Experimental methods and modeling techniques for description of cell population heterogeneity.Engineering strategies aimed at control of acidification rate of lactic acid bacteria.Towards in vivo regulon kinetics: PurR activation by 5-phosphoribosyl-α-1-pyrophosphate during purine depletion in Lactococcus lactis.Lid L11 of the glutamine amidotransferase domain of CTP synthase mediates allosteric GTP activation of glutaminase activity.Two nucleoside uptake systems in Lactococcus lactis: competition between purine nucleosides and cytidine allows for modulation of intracellular nucleotide pools.Bacillus halodurans Strain C125 Encodes and Synthesizes Enzymes from Both Known Pathways To Form dUMP Directly from Cytosine Deoxyribonucleotides.Expression of the pyr operon of Lactobacillus plantarum is regulated by inorganic carbon availability through a second regulator, PyrR2, homologous to the pyrimidine-dependent regulator PyrR1.Uracil salvage pathway in Lactobacillus plantarum: Transcription and genetic studies.Plasmid pCS1966, a new selection/counterselection tool for lactic acid bacterium strain construction based on the oroP gene, encoding an orotate transporter from Lactococcus lactis.Repetitive, marker-free, site-specific integration as a novel tool for multiple chromosomal integration of DNA.Transcriptome analysis of the Lactococcus lactis ArgR and AhrC regulons.The orotate transporter encoded by oroP from Lactococcus lactis is required for orotate utilization and has utility as a food-grade selectable marker.Repression of the pyr operon in Lactobacillus plantarum prevents its ability to grow at low carbon dioxide levels.A fermented meat model system for studies of microbial aroma formation.Addition of α-ketoglutarate enhances formation of volatiles by Staphylococcus carnosus during sausage fermentation.Growth and production of volatiles by Staphylococcus carnosus in dry sausages: Influence of inoculation level and ripening time.Two nucleoside transporters in Lactococcus lactis with different substrate specificities.Expression of the pyrG gene determines the pool sizes of CTP and dCTP in Lactococcus lactis.Development of a real-time PCR method coupled with a selective pre-enrichment step for quantification of Morganella morganii and Morganella psychrotolerans in fish products.Ribosomal dimerization factor YfiA is the major protein synthesized after abrupt glucose depletion in Lactococcus lactis.Interplay Between Capsule Expression and Uracil Metabolism in Streptococcus pneumoniae D39.Design of cAMP-CRP-activated promoters in Escherichia coli.Dispersive solid phase extraction combined with ion-pair ultra high-performance liquid chromatography tandem mass spectrometry for quantification of nucleotides in Lactococcus lactisMulti-stress resistance in Lactococcus lactis is actually escape from purine-induced stress sensitivityThe pH-unrelated influence of salt, temperature and manganese on aroma formation by Staphylococcus xylosus and Staphylococcus carnosus in a fermented meat model systemA simplified method for rapid quantification of intracellular nucleoside triphosphates by one-dimensional thin-layer chromatography
P50
Q24651020-AB405E11-4A2D-4585-B14D-F24516334164Q27312534-EC7B77B3-0E45-4ADB-B712-86FC4923A5DDQ28655650-8032F388-93E7-4AAC-A021-7E6839A65432Q30396867-30F29D1D-B46B-4771-B8F6-C10EB6F77391Q34011333-6A6E55BD-71BA-416D-B557-FE5FBCBB8260Q34639021-4B40F444-AE44-4247-9A08-507F0F7FA1A5Q36349461-32C02C56-6184-4104-BD3A-710BD6866295Q37871683-D1277381-ABAC-4705-B6C0-F7E3856FA0F5Q38069704-51D0509D-2DA5-4E26-936E-78238B455F5EQ38307834-20C120AF-EB2D-4D28-951D-9FA20A78DAA8Q38331445-2FB851B9-DEF3-4BDA-8DAF-02592045CAA7Q39726115-5A9B75D4-E1E0-4A33-B3EB-275D30BAD1EAQ39891763-D39E85C7-E40C-48AF-B6D0-4EE58884A2AFQ41064703-8543CB3A-8665-433B-873C-02DBEACF60FFQ41668538-72AB7303-D8B7-415E-9B28-49D02A61A9A8Q41768365-8E52F602-C49F-4883-8F0C-532017CDF564Q41844630-7222DA01-A22B-401D-8731-3295C0D5DA0BQ42062317-D9566B7E-2EA7-4052-BBEF-D0D961F42B25Q42636047-21C623B3-6AAB-4CC8-8330-F195F4C7C7EDQ42704098-C001B061-37F0-49A5-AD0D-B3498087D0F2Q42724318-7E55A99B-503F-43E1-9F40-DAA4E4771E1AQ42725092-171FA758-038C-45D1-81CE-047D3A6CB750Q42725194-81C1F9CC-1C78-47F0-911A-EE2B9C0B3A17Q42994526-8238E0F9-91C1-42A8-80BE-7B28D8BCF76FQ44925330-4E6F67C4-3B65-4F3F-B9F3-FE0EC06ACCC3Q46756562-F8AE83BC-03CD-4116-83E5-DF847F919158Q51552428-EE3E7E54-B554-4D7A-B06F-AD0799EAF858Q52620569-D4A376F6-3FF1-4C4C-8BF4-27573CD1806DQ54701457-A5F10319-609A-404C-A65D-3CEEDF5E9ED7Q60211482-C1BF428B-F7AF-4C68-9329-F159B344F74DQ63762312-199BFE9A-DE2F-4E3B-84DD-C6D9842B6725Q80966990-DFB53748-E4DA-4F5C-A5F7-5D6EC5114620Q82238089-CFB4591B-5033-49BF-9B6F-504F3C852528
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Jan Martinussen
@ast
Jan Martinussen
@en
Jan Martinussen
@es
Jan Martinussen
@nl
Jan Martinussen
@sl
type
label
Jan Martinussen
@ast
Jan Martinussen
@en
Jan Martinussen
@es
Jan Martinussen
@nl
Jan Martinussen
@sl
prefLabel
Jan Martinussen
@ast
Jan Martinussen
@en
Jan Martinussen
@es
Jan Martinussen
@nl
Jan Martinussen
@sl
P1053
I-4738-2013
P106
P21
P31
P3829
P496
0000-0001-6223-9322