Zobrazeno 1 - 10
of 90
pro vyhledávání: '"Glenn A. Berchtold"'
Autor:
Frank Rusnak, Cheng Tu, Timothy B. Frigo, Christopher T. Walsh, Masahiro Sakaitani, Nina Quinn, Glenn A. Berchtold
Publikováno v:
Biochemistry. 29:6789-6798
The enzyme 2,3-dihydro-2,3-dihydroxybenzoate dehydrogenase (2,3-diDHB dehydrogenase, hereafter Ent A), the product of the enterobactin biosynthetic gene entA, catalyzes the NAD(+)-dependent oxidation of the dihydroaromatic substrate 2,3-dihydro-2,3-d
Autor:
Robert E. Padykula, Robert A. Aleksejczyk, William F. Busby, Glenn A. Berchtold, Ellen K. Stevens, Jia-Sheng Wang
Publikováno v:
Carcinogenesis. 11:1473-1478
Metabolic activation of benzene may occur by a pathway analogous to that accepted for polynuclear aromatic hydrocarbons (PAHs) involving ring epoxidation, enzymatic hydrolysis to the dihydrodiol, and further epoxidation to the diolepoxide. This hypot
Publikováno v:
Biochemistry. 29(6)
Isochorismate synthase (EC 5.4.99.6), the entC gene product of Escherichia coli, catalyzes the conversion of chorismate to isochorismate, the first step in the biosynthesis of the powerful iron-chelating agent enterobactin. A sequence-specific deleti
Publikováno v:
Biochemistry. 29(6)
The Escherichia coli entB, coding for the enterobactin biosynthetic enzyme isochorismatase, has been subcloned into the multicopy plasmid pKK223-3 under the control of the tac promoter. The resulting recombinant plasmid pFR1 expresses isochorismatase
Autor:
Cheng Tu, Glenn A. Berchtold
Publikováno v:
The Journal of Organic Chemistry. 58:6915-6916
Autor:
Daniel E. Piccolo, Herman J. C. Yeh, Alan M. Jeffrey, Glenn A. Berchtold, Donald M. Jerina, Robert M. DeMarinis, Charles H. Foster
Publikováno v:
Journal of the American Chemical Society. 96:6929-6937
Publikováno v:
The Journal of Organic Chemistry. 54:2787-2793
Publikováno v:
The Journal of Organic Chemistry. 46:1817-1820
Autor:
Glenn A. Berchtold, Herbert S. I. Chao
Publikováno v:
The Journal of Organic Chemistry. 46:1191-1194
Autor:
Glenn A. Berchtold, John L. Pawlak
Publikováno v:
The Journal of Organic Chemistry. 53:4063-4069
Le compose du titre est synthetise a partir de la cycloheptanone. La pyrolyse de son ester de dimethyle est effectuee