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1.
FEMS Microbiol Rev ; 47(1)2023 01 16.
Article in English | MEDLINE | ID: mdl-36323406

ABSTRACT

Prochlorococcus and Synechococcus are the two most abundant photosynthetic organisms on Earth, with a strong influence on the biogeochemical carbon and nitrogen cycles. Early reports demonstrated the streamlining of regulatory mechanisms in nitrogen metabolism and the removal of genes not strictly essential. The availability of a large series of genomes, and the utilization of latest generation molecular techniques have allowed elucidating the main mechanisms developed by marine picocyanobacteria to adapt to the environments where they thrive, with a particular interest in the strains inhabiting oligotrophic oceans. Given that nitrogen is often limited in those environments, a series of studies have explored the strategies utilized by Prochlorococcus and Synechococcus to exploit the low concentrations of nitrogen-containing molecules available in large areas of the oceans. These strategies include the reduction in the GC and the cellular protein contents; the utilization of truncated proteins; a reduced average amount of N in the proteome; the development of metabolic mechanisms to perceive and utilize nanomolar nitrate concentrations; and the reduced responsiveness of key molecular regulatory systems such as NtcA to 2-oxoglutarate. These findings are in sharp contrast with the large body of knowledge obtained in freshwater cyanobacteria. We will outline the main discoveries, stressing their relevance to the ecological success of these important microorganisms.


Subject(s)
Nitrogen , Synechococcus , Nitrogen/metabolism , Synechococcus/genetics , Synechococcus/metabolism , Oceans and Seas , Adaptation, Physiological , Nitrates/chemistry , Nitrates/metabolism
2.
ISME J ; 14(5): 1065-1073, 2020 05.
Article in English | MEDLINE | ID: mdl-32034281

ABSTRACT

Marine picocyanobacteria of the Prochlorococcus and Synechococcus genera have been longtime considered as autotrophic organisms. However, compelling evidence published over the last 15 years shows that these organisms can use different organic compounds containing key elements to survive in oligotrophic oceans, such as N (amino acids, amino sugars), S (dimethylsulfoniopropionate, DMSP), or P (ATP). Furthermore, marine picocyanobacteria can also take up glucose and use it as a source of carbon and energy, despite the fact that this compound is devoid of limiting elements and can also be synthesized by using standard metabolic pathways. This review will outline the main findings suggesting mixotrophy in the marine picocyanobacteria Prochlorococcus and Synechococcus, and its ecological relevance for these important primary producers.


Subject(s)
Cyanobacteria/metabolism , Prochlorococcus/metabolism , Synechococcus/metabolism , Carbon Cycle , Oceans and Seas , Seawater/microbiology , Sulfonium Compounds
3.
Biochim Biophys Acta ; 1568(3): 237-44, 2001 Dec 19.
Article in English | MEDLINE | ID: mdl-11786230

ABSTRACT

The inactivation of glutamine synthetase (GS; EC 6.3.1.2) by metal-catalyzed oxidation (MCO) systems was studied in several Prochlorococcus strains, including the axenic PCC 9511. GS was inactivated in the presence of various oxidative systems, either enzymatic (as NAD(P)H+NAD(P)H-oxidase+Fe(3+)+O(2)) or non-enzymatic (as ascorbate+Fe(3+)+O(2)). This process required the presence of oxygen and a metal cation, and is prevented under anaerobic conditions. Catalase and peroxidase, but not superoxide dismutase, effectively protected the enzyme against inactivation, suggesting that hydrogen peroxide mediates this mechanism, although it is not directly responsible for the reaction. Addition of azide (an inhibitor of both catalase and peroxidase) to the MCO systems enhanced the inactivation. Different thiols induced the inactivation of the enzyme, even in the absence of added metals. However, this inactivation could not be reverted by addition of strong oxidants, as hydrogen peroxide or oxidized glutathione. After studying the effect of addition of the physiological substrates and products of GS on the inactivation mechanism, we could detect a protective effect in the case of inorganic phosphate and glutamine. Immunochemical determinations showed that the concentration of GS protein significantly decreased by effect of the MCO systems, indicating that inactivation precedes the degradation of the enzyme.


Subject(s)
Glutamate-Ammonia Ligase/biosynthesis , Gram-Negative Oxygenic Photosynthetic Bacteria/enzymology , Metals/pharmacology , Anaerobiosis , Cations , Enzyme Inhibitors/pharmacology , Ferric Compounds/pharmacology , Ferrous Compounds/pharmacology , Gene Expression Regulation, Enzymologic/drug effects , Glutamate-Ammonia Ligase/analysis , Glutamate-Ammonia Ligase/antagonists & inhibitors , Oxidation-Reduction , Sulfhydryl Compounds/pharmacology
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