Unknown

Dataset Information

0

Characterization of an oxygen-stable nitrogenase complex isolated from Azotobacter chroococcum.


ABSTRACT: In crude cell-free extracts of Azotobacter chroococcum, nitrogenase was much less sensitive to irreversible inactivation by O2 than was the purified enzyme. When nitrogenase was partially purified by anaerobic discontinuous sucrose-density-gradient centrifugation, O2-tolerance was retained. This preparation was considerably enriched in four polypeptides, three of which were derived from the Mo-Fe(molybdenum-iron) protein and Fe (iron) protein of nitrogenase. The fourth was purified to homogeneity and shown to be an iron-sulphur protein (mol.wt. 14000) probably containing a 2Fe--2S centre. When this protein was added to purified nitrogenase, the enzyme was rendered O2-tolerant, through stabilization was Mg2+-dependent. The isolated O2-tolerant nitrogenase was an equimolar stoicheiometric complex between the MO--Fe, Fe and protective proteins. It is likely that the formation of this complex in vivo is the mechanism of 'conformational protection' in this organism.

SUBMITTER: Robson RL 

PROVIDER: S-EPMC1161196 | biostudies-other | 1979 Sep

REPOSITORIES: biostudies-other

Similar Datasets

| S-EPMC1135657 | biostudies-other
| S-EPMC3887007 | biostudies-literature
| S-EPMC4465626 | biostudies-literature
| PRJNA200985 | ENA
| S-EPMC4563567 | biostudies-literature
| S-EPMC7225537 | biostudies-literature
| S-EPMC7385640 | biostudies-literature
| S-EPMC1147972 | biostudies-other
| S-EPMC1148769 | biostudies-other
| S-EPMC1133492 | biostudies-other