@article{MTMT:32772087, title = {EVALUATION OF STRUCTURAL CARBOHYDRATE DEGRADING CAPACITY OF PGP BACTERIAL STRAINS USING DIFFERENT METHODS}, url = {https://m2.mtmt.hu/api/publication/32772087}, author = {Becze, Annamária and Vincze, Éva-Boglárka and Lányi, Szabolcs and Mara, G.}, journal-iso = {UPB SCI BULL SER B}, journal = {UPB SCIENTIFIC BULLETIN, SERIES B: CHEMISTRY AND MATERIALS SCIENCE}, volume = {84}, unique-id = {32772087}, issn = {1454-2331}, year = {2022}, eissn = {1454-2331}, pages = {3-18} } @article{MTMT:31936624, title = {Production of High Added-Value Chemicals in Basfia succiniciproducens: Role of Medium Composition}, url = {https://m2.mtmt.hu/api/publication/31936624}, author = {Bartos, Hunor and Balázs, Márta and Kuzman, Ildikó Hajnalka and Lányi, Szabolcs and Miklóssy, Ildikó}, doi = {10.3390/su13063513}, journal-iso = {SUSTAINABILITY-BASEL}, journal = {SUSTAINABILITY}, volume = {13}, unique-id = {31936624}, year = {2021}, eissn = {2071-1050}, orcid-numbers = {Bartos, Hunor/0000-0002-4183-5181; Miklóssy, Ildikó/0000-0002-8037-7216} } @{MTMT:31913311, title = {Lactobacillus plantarum subsp. plantarum használata haszonnövények silózási folyamataiban}, url = {https://m2.mtmt.hu/api/publication/31913311}, author = {Albert, Beáta and Lányi, Szabolcs and Máthé, István and Laslo, Éva and Orbán, Kálmán Csongor and Bodor, Zsolt and Tánczos, Szidónia and Fejér, Király Gergely and Koncz, Mihály and Tóro, Szabolcs and Funkenhauser, Bernadett and Dobri, Emőke}, unique-id = {31913311}, year = {2019}, orcid-numbers = {Bodor, Zsolt/0000-0003-1386-6957} } @{MTMT:31913310, title = {Az sp. SZX 102 Bacillus törzs használata a haszonnövények silózási folyamataiban}, url = {https://m2.mtmt.hu/api/publication/31913310}, author = {Albert, Beáta and Lányi, Szabolcs and Mara, Gyöngyvér and Kovács, Erika and Orbán, Kálmán Csongor and Laslo, Éva and Bálint, Emese and Bodor, Zsolt and Mészáros, Alexandru and Kádár, Attila and Sinkler, Réka and Toro, Szabolcs and Funkenhauser, Bernadett and Becze, Annamária}, unique-id = {31913310}, year = {2019}, orcid-numbers = {Bodor, Zsolt/0000-0003-1386-6957} } @{MTMT:31913285, title = {Az sp. SZE 102A Bacillus törzs használata a haszonnövények silózási folyamataiban}, url = {https://m2.mtmt.hu/api/publication/31913285}, author = {Albert, Beáta and Bálint, Emese and Becze, Annamária and Bodor, Zsolt and Dobri, Emőke and Fejér, Király Gergely and Koncz, Mihály and Kovács, Erika and Lányi, Szabolcs and Laslo, Éva and Mara, Gyöngyvér and Máthé, István and Máthé, Loránd and Mészáros, Alexandru and Orbán, Kálmán Csongor and Tánczos, Szidónia}, unique-id = {31913285}, year = {2019}, orcid-numbers = {Bodor, Zsolt/0000-0003-1386-6957} } @CONFERENCE{MTMT:31356193, title = {Fehérje-fehérje interakció vizsgálata a sejthalál szabályozásában}, url = {https://m2.mtmt.hu/api/publication/31356193}, author = {Salamon, Pál Attila and Miklóssy, Ildikó and Lányi, Szabolcs and Orbán, Kálmán Csongor and Albert, Beáta}, booktitle = {25th International Conference on Chemistry = XXV. Nemzetközi Vegyészkonferencia}, unique-id = {31356193}, year = {2019}, pages = {105} } @article{MTMT:31239040, title = {Biosynthesis BIR3 domain of inhibitor of apoptosis proteins}, url = {https://m2.mtmt.hu/api/publication/31239040}, author = {Nagy, Katalin and Orbán, Kálmán Csongor and Albert, Beáta and Lányi, Szabolcs}, journal = {UPB Sci. Bull., series B}, volume = {81}, unique-id = {31239040}, year = {2019}, pages = {1454-2331} } @article{MTMT:30767357, title = {Model driven analysis of the biosynthesis of 1,4-butanediol from renewable feedstocks in Escherichia coli}, url = {https://m2.mtmt.hu/api/publication/30767357}, author = {Bodor, Zsolt and Lányi, Szabolcs and Albert, Beáta and Bodor, Katalin and Aurelia, Cristina Nechifor and Miklóssy, Ildikó}, doi = {10.37358/rc.70.19.11.7651}, journal-iso = {REV CHIM-BUCHAREST}, journal = {REVISTA DE CHIMIE}, volume = {70}, unique-id = {30767357}, issn = {0034-7752}, year = {2019}, pages = {3808-3817}, orcid-numbers = {Bodor, Zsolt/0000-0003-1386-6957} } @article{MTMT:30765679, title = {METABOLIC ENGINEERING OF E. COLI: INFLUENCE OF GENE DELETIONS AND HETEROLOGOUS GENES ON PHYSIOLOGICAL TRAITS}, url = {https://m2.mtmt.hu/api/publication/30765679}, author = {Sinkler, Réka and Balázs, Márta and Antal, Emőke and Bartos, Hunor and Lányi, Szabolcs and Miklóssy, Ildikó}, doi = {10.24193/subbchem.2019.2.13}, journal-iso = {STUD UNIV BABES-BOLYAI CHEM}, journal = {STUDIA UNIVERSITATIS BABES-BOLYAI CHEMIA}, volume = {64}, unique-id = {30765679}, issn = {1224-7154}, abstract = {1,4-butanediol (BDO) is an important commodity molecule that is used as a platform chemical for the production of polybutylene terephthalate (PBT), elastic fibres (Spandex) and other materials. The homologous enzyme of E. coli, succinyl-CoA synthetase (sucCD) and the heterologous malonyl-CoA reductase from Chloroflexus aurantiacus (mcr) are key enzymes in a heterologous pathway leading to BDO production, which were introduced into a genome-engineered E. coli MG1655(DE3) Delta ldhA, Delta pflB strain. Knowing that the expression of recombinant proteins and gene deletions can significantly influence cellular viability, the present study was carried out to investigate the impact of the two key enzyme expression on deletion strains, helping us to analyze the physiological changes of E. coli strains and providing directions for further optimizations in order to achieve satisfying target product yields.}, keywords = {Escherichia coli; metabolic engineering; 1,4-BUTANEDIOL; heterologous enzyme}, year = {2019}, eissn = {2065-9520}, pages = {159-174} } @article{MTMT:30765654, title = {ENHANCED HETEROLOGOUS EXPRESSION IN E. COLI}, url = {https://m2.mtmt.hu/api/publication/30765654}, author = {Nagy, Katalin and Kovács, Zita and Salamon, Pál Attila and Orbán, Kálmán Csongor and Lányi, Szabolcs and Albert, Beáta}, doi = {10.24193/subbchem.2019.2.09}, journal-iso = {STUD UNIV BABES-BOLYAI CHEM}, journal = {STUDIA UNIVERSITATIS BABES-BOLYAI CHEMIA}, volume = {64}, unique-id = {30765654}, issn = {1224-7154}, abstract = {Apoptotic regulation has been implicated in many human diseases, including cancer, autoimmune disease, inflammation and neuro degradation. Mapping up critical apoptosis regulators is a strategy for the development of new therapies [1, 2].Present work highlights optimization of heterologous expression conditions for the X-linked inhibitor of apoptosis protein (XIAP). Genes of target protein containing pGEX-4T vector was transformed in chemically competent E. coli Rosetta (TM)(DE3)pLysS cells. The recombinant construct contained a glutathione S-transferase (GST) fusion partner, which assured the purification of the protein by affinity chromatography. In the next step we examined the growth dynamics of the expression culture in M9 minimal medium, meanwhile we also determined the appropriate time of induction. Following this we carried out the optimization of expression, examining the expression's effectiveness under different conditions. On the basis of these fermentation experiments the target protein expression was the most prominent at 18 degrees C with 0.2 mM IPTG induction for 12 hours. During large scale fermentation experiments, we followed the optical density (OD), dry cell weight and substrate utilization. Finally, recombinant protein expression inhancement in the presence of 3% ethanol was successfully achieved in bioreactor. In this case the target protein was expressed in inclusion bodies, therefore solubilisation and refolding is necessary.}, keywords = {Optimization; Ethanol; BIOREACTOR; heterologous expression; XIAP}, year = {2019}, eissn = {2065-9520}, pages = {101-110} }