Involvement of Photosystem II in the ammonia metabolism of a heterotrophic cyanobacterium
نویسندگان
چکیده
Herbicides that bind specifically to Photosystem II greatly increased ammonia liberation by a heterotrophic cyanobacterium incubated with methionine sulfoximine anaerobically in light. Comparison of cells incubated under argon and nitrogen indicated that about one-half of the liberated ammonia came from endogenous sources, as well as from dinitrogen fixation. Chromatography of cell extracts revealed a light·induced, general breakdown of cellular proteins in the presence of methionine sulfoximide. Cultures grown on ammonia, and hence free of heterocysts and nitrogenase, liberated ammonia in the dark in nitrogen-free media with methionine sulfoximine and this liberation was inhibited separately by herbicides or light. A combination of light and herbicide, however, also enhanced ammonia liberation by these cells. Herbicidal Photosystem II inhibitors strongly inhibited light·induced assimilation of the ammonia analog, [14 CJmethylamine, by cyanobacteria. These results implicate Photosystem II directly in the ammonia metabolism of this cyanobacterium and suggest that herbicide-binding protein(s) of this system may regulate nitrogen assimilation coordinately with electron transport.
منابع مشابه
Effects of short-time alkaline pretreatment on growth and photosynthesis efficiency of endemic cyanobacterium Fischerella sp. FS 18.
Alkaline pH is one of the most important problems of our aquatic habitat. We used Stigonematalean native cyanobacterium Fischerella sp. FS 18 as our model strain, andstudied it under different alkaline pHs (7, 9 and rarely 11) under two different – short and long- time treatments (24 and 96 hours after inoculation). Spectroscopic results showed that both alkalinity and time affected growth rate...
متن کاملAmmonia triggers photodamage of photosystem II in the cyanobacterium Synechocystis sp. strain PCC 6803.
Ammonia has long been known to be toxic for many photosynthetic organisms; however, the target for its toxicity remains elusive. Here, we show that in the cyanobacterium Synechocystis sp. strain PCC 6803, ammonia triggers a rapid photodamage of photosystem II (PSII). Whereas wild-type cells can cope with this damage by turning on the FtsH2-dependent PSII repair cycle, the FtsH2-deficient mutant...
متن کاملA systems-level analysis of the effects of light quality on the metabolism of a cyanobacterium.
Photosynthetic organisms experience changes in light quantity and light quality in their natural habitat. In response to changes in light quality, these organisms redistribute excitation energy and adjust photosystem stoichiometry to maximize the utilization of available light energy. However, the response of other cellular processes to changes in light quality is mostly unknown. Here, we repor...
متن کاملGenetic Manipulation of the Cyanobacterium Synechocystis sp. PCC 6803 (Development of Strains Lacking Photosystem I for the Analysis of Mutations in Photosystem II).
We have taken a genetic approach to eliminating the presence of photosystem I (PSI) in site-directed mutants of photosystem II (PSII) in the cyanobacterium Synechocystis sp. PCC 6803. By selecting under light-activated heterotrophic conditions, we have inactivated the psaA-psaB operon encoding the PSI reaction center proteins in cells containing deletions of the three psbA genes. We have also i...
متن کاملGenetic Manipulation of the Cyanobacterium Synechocystis sp . PCC 6803 ' Development of Strains Lacking Photosystem I for the Analysis of Mutations in
We have taken a genetic approach to eliminating the presence of photosystem I (PSI) in site-directed mutants of photosystem I I (PSII) in the cyanobacterium Synechocystis sp. PCC 6803. By selecting under light-activated heterotrophic conditions, we have inactivated the psaA-psaS operon encoding the PSI reaction center proteins in cells containing deletions of the three psbA genes. We have also ...
متن کامل