Biogenesis and Ultrastructure of Carboxysomes from Wild Type and Mutants of Synechococcus sp. Strain PCC 7942

Immature inclusions representing three progressive steps of carboxysome biogenesis have been identified in Synechococcus during the period of adaptation to low-CO2 conditions: (a) ring-shaped structures, (b) electron-translucent inclusions with the shape of a carboxysome and the internal orderly arrangement of ribulose-1,5-bisphosphate carboxylase oxygenase (Rubisco) molecules, and (c) carboxysomes with an internal electron-translucent area, which seem to be the penultimate stage of carboxysome maturation. The ability to build up normal carboxysomes is impaired in three (M3, EK6, and D4) of four high-carbon-requiring mutants studied in this work. M3 and EK6 exhibit abundant immature electron-translucent carboxysomes but no mature ones. This finding supports the contention that an open reading frame located 7.5 kb upstream of the gene encoding the large subunit of Rubisco (altered in M3) is involved in the carboxysome composition and confirms the structural role of the small subunit of Rubisco (slightly modified in EK6) in the assembly of these structures. D4 shows few typical carboxysomes and frequent immature types, its genetic lesion affecting the apparently unrelated gene encoding a subunit of phosphoribosyl aminoamidazole carboxylase of the purine biosynthesis pathway. Revertants EK20 (EK6) and RK13 (D4) have normal carboxysomes, which means that the restoration of the ability to grow under low CO2 coincides with the proper assembling of these structures. N5, a transport mutant due to the alteration of the gene encoding subunit 2 of NADH dehydrogenase, shows an increase in the number and size of carboxysomes and frequent bar-shaped ones.

[1]  J. Shively,et al.  Isolation and characterization of a carboxysome shell gene from Thiobacillus neapolitanus , 1994, Molecular microbiology.

[2]  T. Ogawa,et al.  A gene (ccmA) required for carboxysome formation in the cyanobacterium Synechocystis sp. strain PCC6803 , 1994, Journal of bacteriology.

[3]  A. Kaplan,et al.  Inactivation of ccmO in Synechococcus sp. Strain PCC 7942 Results in a Mutant Requiring High Levels of CO2 , 1994, Applied and environmental microbiology.

[4]  M. Badger,et al.  A Mutant Isolated from the Cyanobacterium Synechococcus PCC7942 Is Unable to Adapt to Low Inorganic Carbon Conditions , 1994, Plant physiology.

[5]  A. Kaplan,et al.  High CO2 Concentration Alleviates the Block in Photosynthetic Electron Transport in an ndhB-Inactivated Mutant of Synechococcus sp. PCC 7942 , 1993, Plant physiology.

[6]  M. Orús,et al.  Trichlorfon-Induced Inhibition of Nitrate and Ammonium Uptake in Cyanobacteria , 1993 .

[7]  A. Kaplan,et al.  Phenotypic Complementation of High CO(2)-Requiring Mutants of the Cyanobacterium Synechococcus sp. Strain PCC 7942 by Inosine 5'-Monophosphate. , 1992, Plant physiology.

[8]  M. Badger,et al.  Isolation of a Putative Carboxysomal Carbonic Anhydrase Gene from the Cyanobacterium Synechococcus PCC7942. , 1992, Plant physiology.

[9]  H. Fukuzawa,et al.  A gene homologous to chloroplast carbonic anhydrase (icfA) is essential to photosynthetic carbon dioxide fixation by Synechococcus PCC7942. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[10]  M. Badger,et al.  The CO2 concentrating mechanism in cyanobacteria and microalgae , 1992 .

[11]  M. Badger,et al.  Evidence for the role of carboxysomes in the cyanobacterial CO2-concentrating mechanism , 1991 .

[12]  A. Kaplan,et al.  Molecular analysis of high CO2 requiring mutants : involvement of genes in the region of rbc, including rbcS, in the ability of cyanobacteria to grow under low CO2 , 1991 .

[13]  A. Kaplan,et al.  A model for inorganic carbon fluxes and photosynthesis in cyanobacterial carboxysomes , 1991 .

[14]  A. Kaplan Analysis of high CO2 requiring mutants indicates a central role for the 5′ flanking region of rbc and for the carboxysomes in cyanobacterial photosynthesis , 1990 .

[15]  A. Kaplan,et al.  The 5'-flanking region of the gene encoding the large subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase is crucial for growth of the cyanobacterium Synechococcus sp. strain PCC 7942 at the level of CO2 in air , 1989, Journal of bacteriology.

[16]  J. Williams,et al.  A cyanobacterial mutant requiring the expression of ribulose bisphosphate carboxylase from a photosynthetic anaerobe. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[17]  M. Badger,et al.  Kinetic properties of ribulose 1,5-bisphosphate carboxylase/oxygenase from Anabaena variabilis. , 1980, Archives of biochemistry and biophysics.

[18]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.

[19]  A. Marker,et al.  The use of acetone and methanol in the estimation of chlorophyll in the presence of phaeophytin , 1972 .

[20]  E. Gantt,et al.  Ultrastructure of Blue-Green Algae , 1969, Journal of bacteriology.

[21]  A. Kaplan,et al.  Physiological and Molecular Studies on the Response of Cyanobacteria to Changes in the Ambient Inorganic Carbon Concentration , 1994 .

[22]  A. Kaplan,et al.  A quantitative model for inorganic carbon fluxes and photosynthesis in cyanobacteria , 1989 .

[23]  F. Smith,et al.  COLORIMETRIC METHOD FOR DETER-MINATION OF SUGAR AND RELATED SUBSTANCE , 1956 .