Literature DB >> 16666239

Photosynthesis in Flaveria brownii, a C(4)-Like Species: Leaf Anatomy, Characteristics of CO(2) Exchange, Compartmentation of Photosynthetic Enzymes, and Metabolism of CO(2).

S H Cheng1, B D Moore, G E Edwards, M S Ku.   

Abstract

Light microscopic examination of leaf cross-sections showed that Flaveria brownii A. M. Powell exhibits Kranz anatomy, in which distinct, chloroplast-containing bundle sheath cells are surrounded by two types of mesophyll cells. Smaller mesophyll cells containing many chloroplasts are arranged around the bundle sheath cells. Larger, spongy mesophyll cells, having fewer chloroplasts, are located between the smaller mesophyll cells and the epidermis. F. brownii has very low CO(2) compensation points at different O(2) levels, which is typical of C(4) plants, yet it does show about 4% inhibition of net photosynthesis by 21% O(2) at 30 degrees C. Protoplasts of the three photosynthetic leaf cell types were isolated according to relative differences in their buoyant densities. On a chlorophyll basis, the activities of phosphoenolpyruvate carboxylase and pyruvate, Pi dikinase (carboxylation phase of C(4) pathway) were highest in the larger mesophyll protoplasts, intermediate in the smaller mesophyll protoplasts, and lowest, but still present, in the bundle sheath protoplasts. In contrast, activities of ribulose 1,5-bisphosphate carboxylase, other C(3) cycle enzymes, and NADP-malic enzyme showed a reverse gradation, although there were significant activities of these enzymes in mesophyll cells. As indicated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, the banding pattern of certain polypeptides of the total soluble proteins from the three cell types also supported the distribution pattern obtained by activity assays of these enzymes. Analysis of initial (14)C products in whole leaves and extrapolation of pulse-labeling curves to zero time indicated that about 80% of the CO(2) is fixed into C(4) acids (malate and aspartate), whereas about 20% of the CO(2) directly enters the C(3) cycle. This is consistent with the high activity of enzymes for CO(2) fixation by the C(4) pathway and the substantial activity of enzymes of the C(3) cycle in the mesophyll cells. Therefore, F. brownii appears to have some capacity for C(3) photosynthesis in the mesophyll cells and should be considered a C(4)-like species.

Entities:  

Year:  1988        PMID: 16666239      PMCID: PMC1054860          DOI: 10.1104/pp.87.4.867

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  16 in total

1.  Mitoxantrone for carcinoma of the endometrium: a phase II trial of the Gynecologic Oncology Group.

Authors:  H B Muss; B N Bundy; P J DiSaia; C E Ehrlich
Journal:  Cancer Treat Rep       Date:  1987-02

2.  Effect of pod removal on leaf senescence in soybeans.

Authors:  V A Wittenbach
Journal:  Plant Physiol       Date:  1982-11       Impact factor: 8.340

3.  Pyruvate, pi dikinase in bundle sheath strands as well as in mesophyll cells in maize leaves.

Authors:  K Aoyagi; H Nakamoto
Journal:  Plant Physiol       Date:  1985-07       Impact factor: 8.340

4.  Spectrophotometric characteristics of chlorophylls a and b and their pheophytins in ethanol.

Authors:  J F Wintermans; A de Mots
Journal:  Biochim Biophys Acta       Date:  1965-11-29

5.  Photosynthetic Characteristics of C(3)-C(4) Intermediate Flaveria Species : III. Reduction of Photorespiration by a Limited C(4) Pathway of Photosynthesis in Flaveria ramosissima.

Authors:  M E Rumpho; M S Ku; S H Cheng; G E Edwards
Journal:  Plant Physiol       Date:  1984-08       Impact factor: 8.340

6.  Photosynthetic/Photorespiratory Carbon Metabolism in the C(3)-C(4) Intermediate Species, Moricandia arvensis and Panicum milioides.

Authors:  A S Holaday; R Chollet
Journal:  Plant Physiol       Date:  1983-11       Impact factor: 8.340

7.  Photosynthetic Characteristics of C(3)-C(4) Intermediate Flaveria Species : I. Leaf Anatomy, Photosynthetic Responses to O(2) and CO(2), and Activities of Key Enzymes in the C(3) and C(4) Pathways.

Authors:  M S Ku; R K Monson; R O Littlejohn; H Nakamoto; D B Fisher; G E Edwards
Journal:  Plant Physiol       Date:  1983-04       Impact factor: 8.340

8.  Enzyme activities of the carbon reduction cycle in some photosynthetic organisms.

Authors:  E Latzko; M Gibbs
Journal:  Plant Physiol       Date:  1969-02       Impact factor: 8.340

9.  Purification and characterization of phosphoenolpyruvate carboxylase from maize leaves.

Authors:  K Uedan; T Sugiyama
Journal:  Plant Physiol       Date:  1976-06       Impact factor: 8.340

10.  Separation of mesophyll protoplasts and bundle sheath cells from maize leaves for photosynthetic studies.

Authors:  R Kanai; G E Edwards
Journal:  Plant Physiol       Date:  1973-06       Impact factor: 8.340

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  30 in total

1.  Functional analysis of corn husk photosynthesis.

Authors:  Jasper J L Pengelly; Scott Kwasny; Soumi Bala; John R Evans; Elena V Voznesenskaya; Nuria K Koteyeva; Gerald E Edwards; Robert T Furbank; Susanne von Caemmerer
Journal:  Plant Physiol       Date:  2011-04-21       Impact factor: 8.340

Review 2.  Evolution of the C4 photosynthetic pathway: events at the cellular and molecular levels.

Authors:  Martha Ludwig
Journal:  Photosynth Res       Date:  2013-05-25       Impact factor: 3.573

3.  Interspecific variation in assimilation of (14)CO 2 into C 4 acids by leaves of C 3, C 4 and C 3-C 4 intermediate Flaveria species near the CO 2 compensation concentration.

Authors:  C J Chastain; R Chollet
Journal:  Planta       Date:  1989-08       Impact factor: 4.116

Review 4.  Russ Monson and the evolution of C4 photosynthesis.

Authors:  Rowan F Sage
Journal:  Oecologia       Date:  2021-03-04       Impact factor: 3.225

5.  Photosynthetic Plasticity in Flaveria brownii: Growth Irradiance and the Expression of C(4) Photosynthesis.

Authors:  S H Cheng; B D Moore; J Wu; G E Edwards; M S Ku
Journal:  Plant Physiol       Date:  1989-04       Impact factor: 8.340

6.  Evolution and function of a cis-regulatory module for mesophyll-specific gene expression in the C4 dicot Flaveria trinervia.

Authors:  Meryem Akyildiz; Udo Gowik; Sascha Engelmann; Maria Koczor; Monika Streubel; Peter Westhoff
Journal:  Plant Cell       Date:  2007-11-09       Impact factor: 11.277

7.  Degree of C(4) Photosynthesis in C(4) and C(3)-C(4)Flaveria Species and Their Hybrids : I. CO(2) Assimilation and Metabolism and Activities of Phosphoenolpyruvate Carboxylase and NADP-Malic Enzyme.

Authors:  G T Byrd; R H Brown; J H Bouton; C L Bassett; C C Black
Journal:  Plant Physiol       Date:  1992-10       Impact factor: 8.340

8.  Degree of C(4) Photosynthesis in C(4) and C(3)-C(4)Flaveria Species and Their Hybrids : II. Inhibition of Apparent Photosynthesis by a Phosphoenolpyruvate Carboxylase Inhibitor.

Authors:  R H Brown; G T Byrd; C C Black
Journal:  Plant Physiol       Date:  1992-10       Impact factor: 8.340

9.  Comparative effects of growth irradiance on photosynthesis and leaf anatomy of Flaveria brownii (C4-like), Flaveria linearis (C 3-C 4) and their F 1 hybrid.

Authors:  J L Araus; H R Brown; G T Byrd; M D Serret
Journal:  Planta       Date:  1991-03       Impact factor: 4.116

10.  Leaf anatomical characteristics in Flaveria trinervia (C4), Flaveria brownii (C 4-like) and their F 1 hybrid.

Authors:  J L Araus; R H Brown; J H Bouton; M D Serret
Journal:  Photosynth Res       Date:  1990-10       Impact factor: 3.573

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