» Articles » PMID: 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)

Overview
Journal Plant Physiol
Specialty Physiology
Date 1988 Aug 1
PMID 16666239
Citations 32
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

Occurrence of distinctive cells and effects of irradiance on vascular formation in leaves of shade-tolerant C grass Paspalum conjugatum.

Hongo A, Abe H, Yabiku T, Ueno O J Plant Res. 2023; 136(5):691-704.

PMID: 37368133 DOI: 10.1007/s10265-023-01475-3.


The Evolution of C4 Photosynthesis in Flaveria (Asteraceae): Insights from the Flaveria linearis Complex.

Adachi S, Stata M, Martin D, Cheng S, Liu H, Zhu X Plant Physiol. 2022; 191(1):233-251.

PMID: 36200882 PMC: 9806627. DOI: 10.1093/plphys/kiac467.


Salt stress induces Kranz anatomy and expression of C photosynthetic enzymes in the amphibious sedge Eleocharis vivipara.

Takao K, Shirakura H, Hatakeyama Y, Ueno O Photosynth Res. 2022; 153(1-2):93-102.

PMID: 35352232 DOI: 10.1007/s11120-022-00913-y.


A scheme for C evolution derived from a comparative analysis of the closely related C, C-C intermediate, C-like, and C species in the genus Flaveria.

Munekage Y, Taniguchi Y Plant Mol Biol. 2022; 110(4-5):445-454.

PMID: 35119574 DOI: 10.1007/s11103-022-01246-z.


Metabolic profiles in C3, C3-C4 intermediate, C4-like, and C4 species in the genus Flaveria.

Borghi G, Arrivault S, Gunther M, Medeiros D, DellAversana E, Fusco G J Exp Bot. 2021; 73(5):1581-1601.

PMID: 34910813 PMC: 8890617. DOI: 10.1093/jxb/erab540.


References
1.
Bauwe H, Chollet R . Kinetic properties of phosphoenolpyruvate carboxylase from c(3), c(4), and c(3)-c(4) intermediate species of flaveria (asteraceae). Plant Physiol. 1986; 82(3):695-9. PMC: 1056191. DOI: 10.1104/pp.82.3.695. View

2.
Wintermans J, DE MOTS A . Spectrophotometric characteristics of chlorophylls a and b and their pheophytins in ethanol. Biochim Biophys Acta. 1965; 109(2):448-53. DOI: 10.1016/0926-6585(65)90170-6. View

3.
Kanai R, Edwards G . Separation of mesophyll protoplasts and bundle sheath cells from maize leaves for photosynthetic studies. Plant Physiol. 1973; 51(6):1133-7. PMC: 366418. DOI: 10.1104/pp.51.6.1133. View

4.
Monson R, Schuster W, Ku M . Photosynthesis in Flaveria brownii A.M. Powell : A C(4)-Like C(3)-C(4) Intermediate. Plant Physiol. 1987; 85(4):1063-7. PMC: 1054394. DOI: 10.1104/pp.85.4.1063. View

5.
Aoyagi K, Nakamoto H . Pyruvate, pi dikinase in bundle sheath strands as well as in mesophyll cells in maize leaves. Plant Physiol. 1985; 78(3):661-4. PMC: 1064797. DOI: 10.1104/pp.78.3.661. View