Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Jan R. Turner"'
Autor:
Mary C. Broughton, Kathryn P. Crawford, Clive Waldron, Patti Matsushima, Krishna M. Madduri, Richard H. Baltz, Paul Robert Rosteck, Donald J. Merlo, Jan R. Turner
Publikováno v:
Chemistry & Biology. 8(5):487-499
Background: Spinosad is a mixture of novel macrolide secondary metabolites produced by Saccharopolyspora spinosa . It is used in agriculture as a potent insect control agent with exceptional safety to non-target organisms. The cloning of the spinosyn
Publikováno v:
Gene. 146:39-45
Cosmid pOJ436, containing large inserts of Saccharopolyspora spinosa (Ss) DNA, was transferred by conjugation from Escherichia coli to Ss an integrated into the chromosome, apparently by homologous recombination, at high frequencies (10(-5) to 10(-4)
Autor:
Robert Theodore Vasileff, Brown Raymond Frank, J. F. Quay, F. T. Counter, J. A. Webber, E. O. Davidson, Terry D. Lindstrom, Jeffrey S. Kasher, William Henry Walker Lunn, Mitchell I. Steinberg, J. M. Jun. Morin, J. A. Eudaly, Paul W. Ensminger, R. E. Koehler, Allen S. Katner, Michael Dean Kinnick, John K. Swartzendruber, Jan R. Turner, David A. Preston, J. K. Shadle, Walter E. Wright, J. F. Stucky, K. D. Kurz, John L. Ott, Karen M. Zimmerman
Publikováno v:
ChemInform. 22
Publikováno v:
ChemInform. 33
Publikováno v:
ACS Symposium Series ISBN: 9780841237834
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2bfe4f7faf07f564c996324f200dc7c0
https://doi.org/10.1021/bk-2002-0800.ch024
https://doi.org/10.1021/bk-2002-0800.ch024
Publikováno v:
Gene. 183(1-2)
The lactone rings of the polyketides platenolide and tylactone are synthesized by condensation of acetate-, proprionate-, and butyrate-derived precursors. A hybrid tylactone/platenolide synthase was constructed to determine if the choice of substrate
Publikováno v:
Antimicrobial Agents and Chemotherapy. 10:470-475
Selected cephalosporins, including cefamandole, cephaloridine, cephaloglycin, and cefoxitin, were examined for their ability to inhibit the enzymatic activity of and act as substrates for beta-lactamases produced by Enterobacter cloacae and Staphyloc
Publikováno v:
Antimicrobial Agents and Chemotherapy. 19:934-936
Moxalactam was examined as a substrate for 11 β-lactamases. Hydrolysis was shown only with the β-lactamase from Bacillus cereus , a nonpathogenic bacterium. Tobramycin was assayed in tobramycin-moxalactam mixtures by using this β-lactamase.
By conventional laboratory evaluation procedures, the in vitro antibacterial activities of cefamandole and its O -formyl ester, cefamandole nafate, appear virtually identical. When the activities of these two compounds were examined for their ability
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cb92485520c4327b60052f659de1370
https://europepmc.org/articles/PMC352155/
https://europepmc.org/articles/PMC352155/