Literature DB >> 16704997

Functional characterization of phosphoenolpyruvate carboxykinase-type C4 leaf anatomy: immuno-, cytochemical and ultrastructural analyses.

Elena V Voznesenskaya1, Vincent R Franceschi, Simon D X Chuong, Gerald E Edwards.   

Abstract

BACKGROUND AND AIMS: Species having C4 photosynthesis belonging to the phosphoenolpyruvate carboxykinase (PEP-CK) subtype, which are found only in family Poaceae, have the most complex biochemistry among the three C4 subtypes. In this study, biochemical (western blots and immunolocalization of some key photosynthetic enzymes) and structural analyses were made on several species to further understand the PEP-CK system. This included PEP-CK-type C4 species Urochloa texana (subfamily Panicoideae), Spartina alterniflora and S. anglica (subfamily Chloridoideae), and an NADP-ME-type C4 species, Echinochloa frumentacea, which has substantial levels of PEP-CK. KEY
RESULTS: Urochloa texana has typical Kranz anatomy with granal chloroplasts scattered around the cytoplasm in bundle sheath (BS) cells, while the Spartina spp. have BS forming long adaxial extensions above the vascular tissue and with chloroplasts in a strictly centrifugal position. Despite some structural and size differences, in all three PEP-CK species the chloroplasts in mesophyll and BS cells have a similar granal index (% appressed thylakoids). Immunolocalization studies show PEP-CK (which catalyses ATP-dependent decarboxylation) is located in the cytosol, and NAD-ME in the mitochondria, in BS cells, and in the BS extensions of Spartina. In the NADP-ME species E. frumentacea, PEP-CK is also located in the cytosol of BS cells, NAD-ME is very low, and the source of ATP to support PEP-CK is not established.
CONCLUSIONS: Representative PEP-CK species from two subfamilies of polyphyletic origin have very similar biochemistry, compartmentation and chloroplast grana structure. Based on the results with PEP-CK species, schemes are presented with mesophyll and BS chloroplasts providing equivalent reductive power which show bioenergetics of carbon assimilation involving C4 cycles (PEP-CK and NAD-ME, the latter functioning to generate ATP to support the PEP-CK reaction), and the consequences of any photorespiration.

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Year:  2006        PMID: 16704997      PMCID: PMC2803547          DOI: 10.1093/aob/mcl096

Source DB:  PubMed          Journal:  Ann Bot        ISSN: 0305-7364            Impact factor:   4.357


  17 in total

1.  Localization of glycerate kinase and some enzymes for sucrose synthesis in c(3) and c(4) plants.

Authors:  H Usuda; G E Edwards
Journal:  Plant Physiol       Date:  1980-05       Impact factor: 8.340

2.  Photosynthetic carbon metabolism of the cool-temperate C4 grass Spartina anglica Hubb.

Authors:  A M Smith; H W Woolhouse; D A Jones
Journal:  Planta       Date:  1982-12       Impact factor: 4.116

3.  NADP-malic enzyme isoforms in maize leaves.

Authors:  V G Maurino; M F Drincovich; C S Andreo
Journal:  Biochem Mol Biol Int       Date:  1996-02

4.  Isolation of Mitochondria from Leaf Tissue of Panicum miliaceum, a NAD-Malic Enzyme Type C(4) Plant.

Authors:  P Gardeström; G E Edwards
Journal:  Plant Physiol       Date:  1983-01       Impact factor: 8.340

5.  A molecular phylogeny of the grass subfamily Panicoideae (Poaceae) shows multiple origins of C4 photosynthesis.

Authors:  L M Giussani; J H Cota-Sánchez; F O Zuloaga; E A Kellogg
Journal:  Am J Bot       Date:  2001-11       Impact factor: 3.844

6.  NADP-malic enzyme and Hsp70: co-purification of both proteins and modification of NADP-malic enzyme properties by association with Hsp70.

Authors:  María V Lara; María F Drincovich; Gabriela L Müller; Verónica G Maurino; Carlos S Andreo
Journal:  Plant Cell Physiol       Date:  2005-04-19       Impact factor: 4.927

7.  Determination of NAD Malic Enzyme in Leaves of C(4) Plants : EFFECTS OF MALATE DEHYDROGENASE AND OTHER FACTORS.

Authors:  M D Hatch; M Tsuzuki; G E Edwards
Journal:  Plant Physiol       Date:  1982-02       Impact factor: 8.340

8.  Comparison of leaf structure and photosynthetic characteristics of C3 and C4 Alloteropsis semialata subspecies.

Authors:  O Ueno; N Sentoku
Journal:  Plant Cell Environ       Date:  2006-02       Impact factor: 7.228

9.  Cloning and analysis of the C4 photosynthetic NAD-dependent malic enzyme of amaranth mitochondria.

Authors:  J J Long; J L Wang; J O Berry
Journal:  J Biol Chem       Date:  1994-01-28       Impact factor: 5.157

10.  Photosynthesis in Phosphoenolpyruvate carboxykinase-type C4 plants: mechanism and regulation of C4 acid decarboxylation in bundle sheath cells.

Authors:  N W Carnal; A Agostino; M D Hatch
Journal:  Arch Biochem Biophys       Date:  1993-11-01       Impact factor: 4.013

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  9 in total

1.  Investigating the NAD-ME biochemical pathway within C4 grasses using transcript and amino acid variation in C4 photosynthetic genes.

Authors:  Alexander Watson-Lazowski; Alexie Papanicolaou; Robert Sharwood; Oula Ghannoum
Journal:  Photosynth Res       Date:  2018-08-04       Impact factor: 3.573

2.  Co-regulation of dark and light reactions in three biochemical subtypes of C(4) species.

Authors:  Olavi Kiirats; David M Kramer; Gerald E Edwards
Journal:  Photosynth Res       Date:  2010-06-12       Impact factor: 3.573

3.  Significant involvement of PEP-CK in carbon assimilation of C4 eudicots.

Authors:  Riyadh Muhaidat; Athena D McKown
Journal:  Ann Bot       Date:  2013-02-06       Impact factor: 4.357

4.  Does Bienertia cycloptera with the single-cell system of C(4) photosynthesis exhibit a seasonal pattern of delta (13)C values in nature similar to co-existing C (4) Chenopodiaceae having the dual-cell (Kranz) system?

Authors:  Hossein Akhani; María Valeria Lara; Maryam Ghasemkhani; Hubert Ziegler; Gerald E Edwards
Journal:  Photosynth Res       Date:  2008-10-25       Impact factor: 3.573

5.  Revealing diversity in structural and biochemical forms of C4 photosynthesis and a C3-C4 intermediate in genus Portulaca L. (Portulacaceae).

Authors:  Elena V Voznesenskaya; Nuria K Koteyeva; Gerald E Edwards; Gilberto Ocampo
Journal:  J Exp Bot       Date:  2010-06-30       Impact factor: 6.992

6.  The activities of PEP carboxylase and the C4 acid decarboxylases are little changed by drought stress in three C4 grasses of different subtypes.

Authors:  Ana E Carmo-Silva; Anabela Bernardes da Silva; Alfred J Keys; Martin A J Parry; Maria C Arrabaça
Journal:  Photosynth Res       Date:  2008-07-16       Impact factor: 3.573

7.  The energy budget in C4 photosynthesis: insights from a cell-type-specific electron transport model.

Authors:  Xinyou Yin; Paul C Struik
Journal:  New Phytol       Date:  2018-03-09       Impact factor: 10.151

Review 8.  How Light Reactions of Photosynthesis in C4 Plants Are Optimized and Protected under High Light Conditions.

Authors:  Wioleta Wasilewska-Dębowska; Maksymilian Zienkiewicz; Anna Drozak
Journal:  Int J Mol Sci       Date:  2022-03-26       Impact factor: 5.923

9.  A molecular phylogeny of the genus Alloteropsis (Panicoideae, Poaceae) suggests an evolutionary reversion from C4 to C3 photosynthesis.

Authors:  Douglas G Ibrahim; Terry Burke; Brad S Ripley; Colin P Osborne
Journal:  Ann Bot       Date:  2008-10-30       Impact factor: 4.357

  9 in total

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