Glycolate metabolism in young and old tobacco leaves, and effects of α-hydroxy-2-pyridinemethanesulfonic acid

1973 ◽  
Vol 51 (10) ◽  
pp. 1857-1865 ◽  
Author(s):  
Marvin L. Salin ◽  
Peter H. Homann

Young tobacco leaves photorespire less than older leaves. This difference is reflected by lower activities of photorespiratory enzymes in young leaves, and by an apparent inability to synthesize glycolate, the substrate of photorespiration.It is shown in this paper that young tobacco leaves differ from old ones in the following, additional respects: (1) extracts have a much lower ability to decarboxylate glycine; (2) the transient burst of CO2 after lowering of the light intensity is nearly absent; (3) photosynthesis is much less inhibited when leaves are floated on solutions of the inhibitor of glycolate oxidase α-hydroxy-2-pyridinemethanesulfonic acid (HPMS); (4) the CO2 compensation concentration is higher; and (5) the mesophyll cells are much more densely packed.It is concluded that the small photorespiratory gas exchange of young leaves is due to deficiencies in enzymes of glycolate metabolism and perhaps to a slow synthesis of glycolate. The latter may be explained by a relatively high internal CO2 concentration resulting from large physical resistances to gas exchange in the tissue. However, the rate of glycolate formation possibly is underestimated because of a low permeability of young leaf tissue to HPMS.Other results provide evidence that HPMS alters the biochemical pattern of CO2 photoassimilation in old tobacco leaves under certain conditions. Hence, this poison ought to be used with caution in studies on photorespiration and glycolate metabolism.


1970 ◽  
Vol 48 (6) ◽  
pp. 1219-1226 ◽  
Author(s):  
D. W. Rehfeld ◽  
D. D. Randall ◽  
N. E. Tolbert

Extracts, mainly from mesophyll cells, were obtained by grinding cells in a Waring Blendor; then extracts of parenchyma sheath cells were obtained by exhaustive grinding of the blender residue in a roller mill or mortar with sand. The specific activities of P-glycolate phosphatase, glycolate oxidase, catalase and reduced nicotinamide adenine dinucleotide- (NADH-) hydroxypyruvate reductase were fourfold higher in extracts of the parenchyma sheath cells than in the mesophyll cells from corn, sugarcane, and Atriplex rosea. P-Glycerate phosphatase was mainly located in the mesophyll cells. The total activity of glycolate oxidase in plants without CO2-photorespiration averaged about one-third that found in other plants on a wet-weight basis. Glycolate oxidase activity in Atriplex rosea, without CO2-photorespiration, was about the same as in Atriplex patula, with CO2-photorespiration. It is concluded that enzymes for glycolate metabolism are present in all leaves in substantial amounts and are located in both cell types, although a higher specific activity is in the parenchyma sheath cells. Thus it is proposed that photorespiration occurs in all plants, but that CO2 evolution from glycolate metabolism is not manifested in plants which have high levels of activity for the C4-dicarboxylic acid cycle of CO2 fixation.



Author(s):  
R.H.M. Cross ◽  
C.E.J. Botha ◽  
A.K. Cowan ◽  
B.J. Hartley

Senescence is an ordered degenerative process leading to death of individual cells, organs and organisms. The detection of a conditional lethal mutant (achloroplastic) of Hordeum vulgare has enabled us to investigate ultrastructural changes occurring in leaf tissue during foliar senescence.Examination of the tonoplast structure in six and 14 day-old mutant tissue revealed a progressive degeneration and disappearance of the membrane, apparently starting by day six in the vicinity of the mitochondria associated with the degenerating proplastid (Fig. 1.) where neither of the plastid membrane leaflets is evident (arrows, Fig. 1.). At this stage there was evidence that the mitochondrial membranes were undergoing retrogressive changes, coupled with disorganization of cristae (Fig. 2.). Proplastids (P) lack definitive prolamellar bodies. The cytoplasmic matrix is largely agranular, with few endoplasmic reticulum (ER) cisternae or polyribosomal aggregates. Interestingly, large numbers of actively-budding dictysomes, associated with pinocytotic vesicles, were observed in close proximity to the plasmalemma of mesophyll cells (Fig. 3.). By day 14 however, mesophyll cells showed almost complete breakdown of subcellular organelle structure (Fig. 4.), and further evidence for the breakdown of the tonoplast. The final stage of senescence is characterized by the solubilization of the cell wall due to expression and activity of polygalacturonase and/or cellulose. The presence of dictyosomes with associated pinocytotic vesicles formed from the mature face, in close proximity to both the plasmalemma and the cell wall, would appear to support the model proposed by Christopherson for the secretion of cellulase. This pathway of synthesis is typical for secretory glycoproteins.



2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Shenqi Wang ◽  
Zimin Zhou ◽  
Rini Rahiman ◽  
Grace Sheen Yee Lee ◽  
Yuan Kai Yeo ◽  
...  

AbstractDevelopmental outcomes are shaped by the interplay between intrinsic and external factors. The production of stomata—essential pores for gas exchange in plants—is extremely plastic and offers an excellent system to study this interplay at the cell lineage level. For plants, light is a key external cue, and it promotes stomatal development and the accumulation of the master stomatal regulator SPEECHLESS (SPCH). However, how light signals are relayed to influence SPCH remains unknown. Here, we show that the light-regulated transcription factor ELONGATED HYPOCOTYL 5 (HY5), a critical regulator for photomorphogenic growth, is present in inner mesophyll cells and directly binds and activates STOMAGEN. STOMAGEN, the mesophyll-derived secreted peptide, in turn stabilizes SPCH in the epidermis, leading to enhanced stomatal production. Our work identifies a molecular link between light signaling and stomatal development that spans two tissue layers and highlights how an environmental signaling factor may coordinate growth across tissue types.



2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Shugang Zhao ◽  
Hongxia Wang ◽  
Kai Liu ◽  
Linqing Li ◽  
Jinbing Yang ◽  
...  

Abstract Background Tissue culture is an effective method for the rapid breeding of seedlings and improving production efficiency, but explant browning is a key limiting factor of walnut tissue culture. Specifically, the polymerization of PPO-derived quinones that cause explant browning of walnut is not well understood. This study investigated explants of ‘Zanmei’ walnut shoot apices cultured in agar (A) or vermiculite (V) media, and the survival percentage, changes in phenolic content, POD and PPO activity, and JrPPO expression in explants were studied to determine the role of PPO in the browning of walnut explants. Results The results showed that the V media greatly reduced the death rate of explants, and 89.9 and 38.7% of the explants cultured in V media and A media survived, respectively. Compared with that of explants at 0 h, the PPO of explants cultured in A was highly active throughout the culture, but activity in those cultured in V remained low. The phenolic level of explants cultured in A increased significantly at 72 h but subsequently declined, and the content in the explants cultured in V increased to a high level only at 144 h. The POD in explants cultured in V showed high activity that did not cause browning. Gene expression assays showed that the expression of JrPPO1 was downregulated in explants cultured in both A and V. However, the expression of JrPPO2 was upregulated in explants cultured in A throughout the culture and upregulated in V at 144 h. JrPPO expression analyses in different tissues showed that JrPPO1 was highly expressed in stems, young leaves, mature leaves, catkins, pistils, and hulls, and JrPPO2 was highly expressed in mature leaves and pistils. Moreover, browning assays showed that both explants in A and leaf tissue exhibited high JrPPO2 activity. Conclusion The rapid increase in phenolic content caused the browning and death of explants. V media delayed the rapid accumulation of phenolic compounds in walnut explants in the short term, which significantly decreased explants mortality. The results suggest that JrPPO2 plays a key role in the oxidation of phenols in explants after branch injury.



1999 ◽  
Vol 54 (9-10) ◽  
pp. 688-692 ◽  
Author(s):  
Konstantinos Chartzoulakis ◽  
Angelos Patakas ◽  
Artemis Bosabalidis

The effect of water stress on gas exchange, water relations and leaf anatomical characteristics have been studied in two olive cultivars (Olea europea, L. cv. ‘Koroneiki’ and cv. ‚Mastoidis’). Photosynthetic rate as well as stomatal conductance were decreased in stressed plants. Osmotic potential (π) declined rapidly in stressed plants indicating their ability for osmoregulation. Bulk modulus of elasticity (ε) was significantly higher in stressed compared to well irrigated plants. The volume fraction of intercellular spaces of the upper palisade parenchyma, the spongy parenchyma as well as the lower palisade parenchyma were significantly lower in stressed compared to well irrigated plants. On the other hand, the density of mesophyll cells in the upper palisade parenchyma, spongy parenchyma and lower palisade parenchyma increased significantly in stressed plants



Hoehnea ◽  
2017 ◽  
Vol 44 (2) ◽  
pp. 236-245 ◽  
Author(s):  
Juliana Moreno Pina ◽  
Sérgio Tadeu Meirelles ◽  
Regina Maria de Moraes

ABSTRACT This study aimed to investigate the importance of leaf age, meteorological conditions and ozone concentration (O3) on gas exchange of Psidium guajava ‛Paluma'. Saplings were grown and exposed in standard conditions in the city of São Paulo, in six periods of three months with weekly measurements in young and mature leaves. Gas exchanges were higher in young leaves for almost the entire experiment. Mature leaves showed greater reduction in gas exchange. The multivariate analysis of biotic and abiotic variables indicated that vapor pressure deficit (VPD), O3 concentration and radiation were the main variables associated with gas exchange decrease in young leaves. In mature leaves the influence of VPD is lower, but the temperature importance is higher. Moreover, the opposition between assimilation and O3 is more evident in mature leaves, indicating their greater sensitivity to O3.



2019 ◽  
Vol 15 (11) ◽  
Author(s):  
Thays Saynara Alves Menezes-Sá ◽  
Maria de Fátima Arrigoni-Blank ◽  
Andréa Santos da Costa ◽  
Janay De Almeida Santos-Serejo ◽  
Arie Fitzgerald Blank ◽  
...  

Chromosome doubling induction in orchids may benefit their production for resulting in flowers of higher commercial value, larger size and higher content of substances that intensify the color and fragrance when compared with diploid orchids. This work aimed to induce and confirm artificial polyploidization, using flow cytometry and stomatal analysis. Explants were treated with colchicine at concentrations of 0, 2.5, 7.5, and 12.5 mM, for 24 and 48 hours and with oryzalin, at concentrations of 0, 10, 30, and 50 μM, for three and six days. For the flow cytometric analysis, a sample of leaf tissue was removed from each plant, crushed to release the nuclei and stained with propidium iodide. In addition to flow cytometry, the ploidy of the antimitotic treated plants was evaluated by stomata analysis. Young leaves were used where the density, functionality and stomatal index were evaluated. Colchicine provided induction of satisfactory polyploidy in C. tigrina at all concentrations and times of exposure, obtaining a greater number of polyploid individuals in the concentration of 12.5 mM for 48 hours. Oryzalin did not induce chromosome duplication at the tested concentrations.



2010 ◽  
Vol 40 (6) ◽  
pp. 1290-1294 ◽  
Author(s):  
Inês Cechin ◽  
Natália Corniani ◽  
Terezinha de Fátima Fumis ◽  
Ana Catarina Cataneo

The effects of water stress and rehydration on leaf gas exchange characteristics along with changes in lipid peroxidation and pirogalol peroxidase (PG-POD) were studied in mature and in young leaves of sunflower (Helianthus annuus L.), which were grown in a greenhouse. Water stress reduced photosynthesis (Pn), stomatal conductance (g s), and transpiration (E) in both young and mature leaves. However, the amplitude of the reduction was dependent on leaf age. The intercellular CO2 concentration (Ci) was increased in mature leaves but it was not altered in young leaves. Instantaneous water use efficiency (WUE) in mature stressed leaves was reduced when compared to control leaves while in young stressed leaves it was maintained to the same level as the control. After 24h of rehydration, most of the parameters related to gas exchange recovered to the same level as the unstressed plants except gs and E in mature leaves. Water stress did not activated PG-POD independently of leaf age. However, after rehydration the enzyme activity was increased in mature leaves and remained to the same as the control in young leaves. Malondialdehyde (MDA) content was increased by water stress in both mature and young leaves. The results suggest that young leaves are more susceptible to water stress in terms of gas exchange characteristics than mature leaves although both went through oxidative estresse.



1984 ◽  
Vol 62 (3) ◽  
pp. 463-474 ◽  
Author(s):  
C. M. Adams ◽  
N. G. Dengler ◽  
T. C. Hutchinson

The present study describes the effects of simulated acid rain (pH 2.5–5.6) on foliar histology of an arctic herb, Artemisia tilesii Ledeb., which is remarkably tolerant to naturally occurring atmospheric acidity at Smoking Hills, N.W.T. Plants were exposed to simulated acid rain twice weekly for 4 weeks in exposure chambers in the greenhouse. Droplets as acidic as pH 2.5 caused limited macroscopic foliar damage. However, much greater damage was observed when sectioned leaf tissue was examined microscopically. On leaves having no injury visible to the unaided eye, small lesions consisting of one to three collapsed epidermal cells were observed in scanning electron micrographs and in cleared leaves after exposure to rain of pH 3.0 and 3.5. Stomata remained open in damaged areas of acid-sprayed leaves. Lesions most commonly developed from an initial collapse of a few adaxial epidermal cells, followed by progressive injury of underlying tissues. Palisade and spongy mesophyll cells underwent hypertrophic (abnormal cell enlargement) and hyperplastic (abnormal cell division) responses in the region adjacent to severely collapsed tissue, causing reduced intercellular spaces. These effects isolated the injured areas from adjacent healthy tissues, and resembled wound periderm responses to fungal pathogens and to mechanical irritation. This response may be one mechanism of limiting acid rain damage.



2002 ◽  
Vol 42 (2) ◽  
pp. 207 ◽  
Author(s):  
T. Bertozzi ◽  
E. Alberts ◽  
M. Sedgley

The reliability of enzyme-linked immunosorbent assay (ELISA) and indexing methodologies for the detection of Prunus necrotic ringspot virus (PNRSV) in almond was assessed under local conditions. Thirteen field-grown almond trees were sampled fortnightly throughout the growing season. Petal and leaf homogenates were used for ELISA and to inoculate herbaceous indicator species, while buds collected from October onwards were budded to woody indicators. ELISA reliably detected PNRSV in petals and young leaves from bud-break until the cessation of stem elongation. While herbaceous indexing was not as reliable as ELISA, woody indicators could differentiate positive from negative samples reliably throughout the testing period. However, for mass screening of foundation plantings, nursery stock and elite germplasm, woody indexing is too costly and slow to give results. The use of ELISA can overcome these limitations but the timing of sample collection is critical. Petal or leaf tissue collected early in the season will yield the most reliable results.



Sign in / Sign up

Export Citation Format

Share Document