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Immunochemical evidence that nitrogenase is restricted to the heterocysts in Anabaena cylindrica
Authors:Marcia A. Murry  Patrick C. Hallenbeck  John R. Benemann
Affiliation:(1) Sanitary Engieering and Environmental Health Laboratory, University of California, Berkeley, 94720 Berkeley, CA, USA;(2) Present address: Cabot Foundation, Harvard University, 01366 Petersham, MA, USA;(3) Present address: Dept. of Biological Chemistry, School of Medicine, University of California, 95616 Davis, CA, USA;(4) Present address: EnBio, Inc., 408 A Union Avenue, 94533 Fairfield, CA, USA
Abstract:The question of whether the vegetative cells of Anabaena cylindrica synthesize nitrogenase under anaerobic conditions was studied by immunoferritin labelling of the Fe-Mo protein (Component I). Differentiating cultures, incubated under an argon atmosphere, were treated with DCMU 12 h following initiation of induction. DCMU inhibited photosynthetic O2 production, thus insuring strict anaerobic conditions, but had no effect on nitrogenase induction. Fe-Mo protein levels, as determined by rocket immunoelectrophoresis, increased 5-fold within 24h of DCMU treatment. Immunoferritin labelling of aldehyde fixed, ultrathin cryosections of anaerobically induced filaments showed that the Fe-Mo protein was restricted to the heterocyst. Ferritin labelling was shown to be specific by the following criteria: (a) substituting preimmune goat serum for the anti-Fe-Mo protein IgG prevented ferritin labelling; (b) ferritin-conjugated, non-homologous rabbit anti-goat IgG did not bind; (c) incubation of anti-Fe-Mo protein IgG treated sections with rabbit anti-goat IgG prior to the treatment with the ferritin label also prevented labelling. The results provide direct immunochemical evidence that nitrogenase is restricted to the heterocysts even under strictly anaerobic conditions.
Keywords:Heterocysts  Immunoferritin labelling  Cyanobacteria  Anabaena  Nitrogenase
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