Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Galli, E."'
Autor:
BESTETTI, GIUSEPPINA, DI GENNARO, PATRIZIA, Galli, E, Leoni, B, Pelizzoni, F, Sello, G, Bianchi, D.
The Pseudomonas fluorescens N3 was isolated from soil for its ability to utilize naphthalene as a carbon source. The strain transforms 2,3-dimethyl-, 2-methoxy-, 1- and 2-ethylnaphthalenes to the corresponding salicylic acids competitively with chemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1299::f9b251ae55e72747227839fa10c4c000
http://hdl.handle.net/10281/35959
http://hdl.handle.net/10281/35959
Publikováno v:
ResearcherID
We developed a biocatalyst by cloning the styrene monooxygenase genes (styA and styB) from Pseudomonas fluorescens ST responsible for the oxidation of styrene to its corresponding epoxide. Recombinant Escherichia coil was able to oxidize different ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cb9ad20ae37bc8c8aa2f8a7d73308338
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000080624300082&KeyUID=WOS:000080624300082
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000080624300082&KeyUID=WOS:000080624300082
Autor:
Enrica Galli, Giuseppina Bestetti, Patrizia Di Gennaro, Ilaria Ronco, Andrea Colmegna, Guido Sello
Publikováno v:
International Biodeterioration & Biodegradation. 54:183-187
Styrene degradation by Pseudomonas fluorescens ST was determined by analysis of recombinant clones generated. Styrene is degraded via the oxidation of the side chain leading to epoxystyrene, which is subsequently isomerized to phenylacetaldehyde and
Autor:
Debora Berti, P. Di Gennaro, F. Briganti, Enrica Galli, Piero Baglioni, Giuseppina Bestetti, Andrea Scozzafava, D. Randazzo
Publikováno v:
Langmuir. 18:6015-6020
This paper illustrates the use of a nonionic micellar system to enhance the efficiency of a bacterial whole cell oxidation of a polycyclic aromatic substrate. We have studied the biotransformation of naphthalene operated by an isolated strain of an e
Autor:
Piero Baglioni, Patrizia Di Gennaro, Andrea Scozzafava, Fabrizio Briganti, Giuseppina Bestetti, Debora Berti, Enrica Galli, Demetrio Randazzo
Publikováno v:
Journal of Inorganic Biochemistry. 79:103-108
Whole-cell bioconversion of naphthalene to (+)-cis-(1R,2S)-dihydroxy-1,2-dihydronaphthalene by Escherichia coli JM109(pPS1778) recombinant strain, carrying naphthalene dioxygenase and regulatory genes cloned from Pseudomonas fluorescens N3, in direct
Autor:
Andrea Scozzafava, Piero Baglioni, Fabrizio Briganti, Debora Berti, Patrizia Di Gennaro, Enrica Galli, Giuseppina Bestetti, Demetrio Randazzo
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. 7:263-272
The whole cell biological conversion of naphthalene to (+)-cis-(1R,2S)-dihydroxy-1,2-dihydronaphthalene by the E. coli JM109(pPS1778) recombinant strain carrying the naphthalene dioxygenase and regulatory genes cloned from Pseudomonas fluorescens N3
Autor:
Enrica Galli, P. Di Gennaro, Guido Sello, G. Albini, Francesca Pelizzoni, Giuseppina Bestetti
Publikováno v:
Research in Microbiology. 148:355-364
Naphthalene dioxygenase, a key enzyme in the dihydroxylation of naphthalene, is encoded by the plasmid pN3, responsible for naphthalene metabolism in Pseudomonas fluorescens N3. The naphthalene dioxygenase, including all the sequences for its express
Publikováno v:
Biodegradation. 4:71-80
Pseudomonas stutzeri OX1 is able to grow on o-xylene but is unable to grow on m-xylene and p-xylene, which are partially metabolized through the o-xylene degradative pathway leading to the formation of dimethylphenols toxic to OX1. P. stutzeri sponta
Autor:
Enrica Galli, Dafne Solera, Giuseppina Bestetti, Patrizia Di Gennaro, Francesco Renzi, Guido Sello, Silvia Ferrara, Giovanni Bertoni
Publikováno v:
Applied microbiology and biotechnology. 79(4)
Novel expression systems for the development of whole-cell biocatalysts were generated. Their novelty consists both in the host, Pseudomonas putida, and in the ability to auto-induce the expression of genes of interest at the exhaustion of the carbon