Proof of C4 photosynthesis without Kranz anatomy in Bienertia cycloptera (Chenopodiaceae).

Kranz anatomy, with its separation of elements of the C4 pathway between two cells, has been an accepted criterion for function of C4 photosynthesis in terrestrial plants. However, Bienertia cycloptera (Chenopodiaceae), which grows in salty depressions of Central Asian semi-deserts, has unusual chlorenchyma, lacks Kranz anatomy, but has photosynthetic features of C4 plants. Its photosynthetic response to varying CO2 and O2 is typical of C4 plants having Kranz anatomy. Lack of night-time CO2 fixation indicates it is not acquiring carbon by Crassulacean acid metabolism. This species exhibits an independent, novel solution to function of the C4 mechanism through spatial compartmentation of dimorphic chloroplasts, other organelles and photosynthetic enzymes in distinct positions within a single chlorenchyma cell. The chlorenchyma cells have a large, spherical central cytoplasmic compartment interconnected by cytoplasmic channels through the vacuole to the peripheral cytoplasm. This compartment is filled with mitochondria and granal chloroplasts, while the peripheral cytoplasm apparently lacks mitochondria and has grana-deficient chloroplasts. Immunolocalization studies show enzymes compartmentalized selectively in the CC compartment, including Rubisco in chloroplasts, and NAD-malic enzyme and glycine decarboxylase in mitochondria, whereas pyruvate, Pi dikinase of the C4 cycle is localized selectively in peripheral chloroplasts. Phosphoenolpyruvate carboxylase, a cytosolic C4 cycle enzyme, is enriched in the peripheral cytoplasm. Our results show Bienertia utilizes strict compartmentation of organelles and enzymes within a single cell to effectively mimic the spatial separation of Kranz anatomy, allowing it to function as a C4 plant having suppressed photorespiration; this raises interesting questions about evolution of C4 mechanisms.

[1]  H. Akhani,et al.  Photosynthetic pathways inChenopodiaceae from Africa, Asia and Europe with their ecological, phytogeographical and taxonomical importance , 1997, Plant Systematics and Evolution.

[2]  Alison M. Smith,et al.  Distribution of photorespiratory enzymes between bundle-sheath and mesophyll cells in leaves of the C3−C4 intermediate species Moricandia arvensis (L.) DC , 1988, Planta.

[3]  D. Jones,et al.  Glycine decarboxylase is confined to the bundle-sheath cells of leaves of C3−C4 intermediate species , 1988, Planta.

[4]  K. Winter C4 plants of high biomass in arid regions of asia-occurrence of C4 photosynthesis in Chenopodiaceae and Polygonaceae from the Middle East and USSR , 1981, Oecologia.

[5]  E. Ganko,et al.  Occurrence of C3 and C4 photosynthesis in cotyledons and leaves of Salsola species (Chenopodiaceae) , 2004, Photosynthesis Research.

[6]  W. Stichler,et al.  Bienertia cycloptera Bunge ex Boiss., Chenopodiaceae, another C4 Plant without Kranz Tissues286 , 2002 .

[7]  G. Edwards,et al.  Kranz anatomy is not essential for terrestrial C4 plant photosynthesis , 2001, Nature.

[8]  G. Edwards,et al.  Salsola arbusculiformis, a C3–C4Intermediate in Salsoleae (Chenopodiaceae) , 2001 .

[9]  G. Edwards,et al.  Compartmentation of photosynthesis in cells and tissues of C(4) plants. , 2001, Journal of experimental botany.

[10]  R. Furbank,et al.  What Does It Take to Be C 4 ? Lessons from the Evolution of C 4 Photosynthesis , 2001 .

[11]  R. Furbank,et al.  What does it take to be C4? Lessons from the evolution of C4 photosynthesis. , 2001, Plant physiology.

[12]  W. Stichler,et al.  A remarkable new leaf type with unusual photosynthetic tissue in a central Asiatic genus of Chenopodiaceae. , 2000 .

[13]  J. Marôco,et al.  Utilization of O2 in the metabolic optimization of C4 photosynthesis , 2000 .

[14]  G. Edwards,et al.  Anatomy, chloroplast structure and compartmentation of enzymes relative to photosynthetic mechanisms in leaves and cotyledons of species in the tribe salsoleae (Chenopodiaceae) , 1999 .

[15]  R. Monson,et al.  16 – The Taxonomic Distribution of C4 Photosynthesis , 1999 .

[16]  R. Monson,et al.  C[4] plant biology , 1999 .

[17]  G. Hammer,et al.  Correlation between carbon isotope discrimination and transpiration efficiency in lines of the C-4 species Sorghum bicolor in the glasshouse and the field , 1998 .

[18]  V. Maurino,et al.  NADP-malic enzyme isoforms in maize leaves. , 1996, Biochemistry and molecular biology international.

[19]  J J Long,et al.  Cloning and analysis of the C4 photosynthetic NAD-dependent malic enzyme of amaranth mitochondria. , 1994, The Journal of biological chemistry.

[20]  Y. Gamalei,et al.  Effect of salinity on the structure of assimilating organs and 14C labelling patterns in C3 and C4 plants of Ararat plain , 1992 .

[21]  Graham D. Farquhar,et al.  Short-term measurements of carbon isotope discrimination in several C4 species , 1992 .

[22]  J. Ehleringer,et al.  Correlations between Carbon Isotope Discrimination and Leaf Conductance to Water Vapor in Common Beans. , 1990, Plant physiology.

[23]  J. Seemann,et al.  14CO2 Labeling Studies of 2-Carboxyarabinitol 1-Phosphate Synthesis , 1990 .

[24]  M. D. Hatch,et al.  C4 photosynthesis: a unique elend of modified biochemistry, anatomy and ultrastructure , 1987 .

[25]  E. V. Voznesenskaia,et al.  Ultrastructural characteristics of leaf types with Kranz-anatomy , 1986 .

[26]  G. Edwards,et al.  C3, C4: Mechanisms and Cellular and Environmental Regulation of Photosynthesis , 1983 .

[27]  G. Farquhar,et al.  On the Nature of Carbon Isotope Discrimination in C4 Species , 1983 .

[28]  W. N. Burnette,et al.  "Western blotting": electrophoretic transfer of proteins from sodium dodecyl sulfate--polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein A. , 1981, Analytical biochemistry.

[29]  T. A. Glacoleva,et al.  Oxygen effects on photosynthesis and C metabolism in desert plants. , 1978, Plant physiology.

[30]  T. A. Glacoleva,et al.  Oxygen Effects on Photosynthesis and 14C Metabolism in Desert , 1978 .

[31]  J. Troughton,et al.  Leaf anatomy of Atriplex buchananii , 1974 .

[32]  H. Vines,et al.  13C/12C Ratio Changes in Crassulacean Acid Metabolism Plants , 1973 .

[33]  R. Slatyer,et al.  Photosynthesis and photorespiration. , 1971, Science.

[34]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[35]  U. K. Laemmli,et al.  Cleavage of structural proteins during , 1970 .

[36]  P. Schürmann Separation of phosphate esters and algal extracts by thin-layer electrophoresis and chromatography. , 1969, Journal of chromatography.

[37]  V. V. Patwardhan,et al.  The role of elution solvent in quenching of Ittrich estrogen fluorescence reaction observed with silica gel eluates. , 1969, Journal of chromatography.

[38]  W. Laetsch CHLOROPLAST SPECIALIZATION IN DICOTYLEDONS POSSESSING THE C4‐DICARBOXYLIC ACID PATHWAY OF PHOTOSYNTHETIC CO2 FIXATION , 1968 .

[39]  H. Hus Leaf Structure , 1906, The American Naturalist.

[40]  G. Edwards,et al.  Salsola arbusculiformis , a C 3 –C 4 Intermediate in Salsoleae (Chenopodiaceae) , 2022 .

[41]  J. Marôco Utilization of O 2 in the metabolic optimization of C 4 photosynthesis , 2022 .