Unknown

Dataset Information

0

The stereochemistry of beta-lactam formation in cephalosporin biosynthesis.


ABSTRACT: 3H and 14C from (2R,3S)[U-14C,3-3H1]cysteine and (2R,3R)-[U-14C,2,3-3H2]cysteine were incorporated into cephalosporin C by Cephalosporium acremonium. Analysis of the radioactive cephalosporin C indicated that the formation of its beta-lactam ring occurs stereospecifically and with retention of configuration at C-3 of cysteine.

SUBMITTER: Huddleston JA 

PROVIDER: S-EPMC1183844 | biostudies-other | 1978 Mar

REPOSITORIES: biostudies-other

Similar Datasets

| S-EPMC4401618 | biostudies-literature
| S-EPMC8588317 | biostudies-literature
| S-EPMC2610506 | biostudies-literature
| S-EPMC1164653 | biostudies-other
| S-EPMC3961552 | biostudies-literature
| S-EPMC1178863 | biostudies-other
| PRJNA543210 | ENA
| S-EPMC2833277 | biostudies-literature
2014-06-04 | E-GEOD-58213 | biostudies-arrayexpress
| S-EPMC1144242 | biostudies-other