Background
Photosynthesis is controlled by several intrinsic and extrinsic factors. Of these, plant hormones have received considerable attention in the past in photosynthetic responses of plants. Ethylene is a phytohormone that influences every aspect of plant growth and development 1. It is synthesized by the activity of 1-aminocyclopropane carboxylic acid synthase (ACS). The response of plants to ethylene depends on the sensitivity of plants to the gas. Conflicting results on the effects of ethylene-releasing compounds on net photosynthetic rate (PN) have been reported. It has been shown to increase PN 234567 or decrease it 89, but no definite reason has been assigned for this. It has been shown that the increase in PN with ethylene-releasing compounds was due to the increase in chlorophyll per unit leaf area 10 or by greater light interception 11. In my earlier report it has been shown that alteration in photosynthesis was due to the changes in ACS activity 12. The goal of this work was to compare stomatal and mesophyll effects on PN in response to ethephon treatment. For that, PN, stomatal conductance (gS) and carbonic anhydrase (CA) activity were recorded. To find a possible relationship of ethylene-mediated changes in foliar gas exchange parameters, activity of ACS and ethylene evolution were also determined. The work was carried out in two cultivars of mustard previously shown to have different photosynthetic capacity 12.
Results
The effects of ethephon on PN, gS and CA were found significant in both the cultivars (Figures 1, 2). Ethephon at 1.5 mM increased the characteristics maximally, increasing PN by 31.8 and 41.8%, gS by 15.0 and 17.1% and CA by 84.6 and 71.4% in Varuna and RH30, respectively. Higher concentration of ethephon (3.0 mM) decreased the characteristics in both the cultivars. The ratio of intercellular to ambient CO2 concentration (Ci/Ca) was constant.
<p>Figure 1</p>
Effects of ethephon on photosynthesis and stomatal conductance in mustard
Effects of ethephon on photosynthesis and stomatal conductance in mustard Effect of different concentrations of ethephon (2-chloroethyl phosphonic acid) applied at 30 d after sowing on net photosynthetic rate (PN) (A) and stomatal conductance (gS) (B) in high photosynthetic capacity cultivar Varuna and low photosynthetic capacity cultivar RH30 of mustard (Brassica juncea) at 15 d after the treatment. Each data point represent treatment mean ± SE. Values at each data point within the cultivar sharing the same letter are not significantly different at P < 0.05.
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<p>Figure 2</p>
Effects of ethephon on intercellular CO2 concentration and carbonic anhydrase activity in mustard
Effects of ethephon on intercellular CO2 concentration and carbonic anhydrase activity in mustard Effect of different concentrations of ethephon (2-chloroethyl phosphonic acid) applied at 30 d after sowing on intercellular CO2 concentration (Ci) (A) and carbonic anhydrase (CA) activity (B) in high photosynthetic capacity cultivar Varuna and low photosynthetic capacity cultivar RH30 of mustard (Brassica juncea) at 15 d after the treatment. Each data point represent treatment mean ± SE. Values at each data point within the cultivar sharing the same letter are not significantly different at P < 0.05.
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Ethephon application significantly affected ACS activity and ethylene evolution, and were greatest with 3.0 mM ethephon (Table 1). Low photosynthetic capacity cultivar, RH30 was more responsive to ethephon than the high photosynthetic capacity cultivar, Varuna. Application of 1.5 mM ethephon increased ethylene by 52.6% in Varuna and 75.0% in RH30. Increase in ethylene with 1.5 mM ethephon was associated with the increase in PN, gS and CA. Ethylene evolution with 3.0 mM ethephon proved inhibitory for photosynthetic parameters.
<p>Table 1</p>
Effects of different concentrations of ethephon (2-chloroethyl phosphonic acid) applied at 30 d after sowing on the activity of 1-aminocyclopropane carboxylic acid synthase (ACS; (ng ACC kg-1 leaf (FM) s-1) and ethylene evolution (ng kg-1 leaf (FM) s-1) in two cultivars of mustard (Brassica juncea) at 15 d after the treatment. Values ± SE. Data followed by the same letter within a column are significantly not different.
Ethephon Treatments (mM)
High photosynthetic capacity cultivar (Varuna)
Low photosynthetic capacity cultivar (RH 30)
ACS
Ethylene
ACS
Ethylene
0
62.2 ± 5.4c
3.8 ± 0.2c
40.8 ± 3.6c
2.4 ± 0.2c
0.75
64.6 ± 5.8c
4.4 ± 0.3bc
44.4 ± 4.0c
3.2 ± 0.2bc
1.5
68.2 ± 5.8b
5.8 ± 0.3b
52.8 ± 4.6b
4.2 ± 0.3b
3.0
73.5 ± 6.0a
7.0 ± 0.5a
62.3 ± 5.6a
6.0 ± 0.4a
Discussion
Maximum rates of photosynthesis were found with 1.5 mM ethephon. The increase in PN due to ethephon has been reported 456. Increased gs and CA values in both the cultivars showed stomatal and mesophyll effects on photosynthesis. Mesophyll effects are characterized as a product of CO2 binding capacity and the electron transport capacity. The carboxylation capacity determines the mesophyll effects 1314. Increase in CA activity at the site of CO2 fixation exhibited the enhanced carboxylation reaction 151617. The changes in stomatal conductance due to ethephon were to maintain stable intercellular CO2 concentration (Ci) under the given treatment. Thus, stomatal and mesophyll processes contributed to the increase in PN in response to ethephon. The ethephon-induced effects on photosynthetic parameters were mediated by ethylene evolved due to ethephon treatment. Taylor and Gunderson 18 showed a relationship between ethylene-enhanced gS and ethylene-enhanced PN. Higher concentration of ethephon (3.0 mM) decreased the PN and gS. Such condition of inhibition of PN by ethylene-releasing compound has been observed by Kays and Pallas 8 and Rajala and Peltonen-Sainio 9. In all these studies ethylene has been attributed to the changes in PN due to its effect on gS. Mattoo and White 19 reported that ethylene affected CO2 assimilation and the plant responded depending on the tissue concentration. On the similar lines, Dhawan et al. 20, Kao and Yang 21 and Grodzinski et al. 22 reasoned that decrease in CO2 regulated PN and was related to ethylene evolution. In the present study, low photosynthetic cultivar, RH30 responded more to ethephon than the high photosynthetic cultivar, Varuna. In control plants, lesser ethylene evolution in RH30 than Varuna was responsible for lesser PN. As the ethylene evolution increased with ethephon application, the capacity of RH30 for PN also increased resulting in higher per cent increase in PN than the Varuna. An increase of 75% ethylene in RH30 due to 1.5 mM ethephon increased PN by 41.8%, whereas 52.6% increase in ethylene in Varuna due to the same treatment increased PN by 31.8%. Earlier strong positive correlation between ACS activity and PN has been shown 12.
It therefore, appears possible that the threshold value for ethylene with 1.5 mM ethephon was comparable to that which elicits the ethylene-mediated hormonal responses, which differ with the cultivars inherent capacity of physiological processes. It is that there is some requirement of ethylene for optimum response. Low and high concentration represent the two ends of an optimum curve, promoting at low concentration and inhibiting at high.
Conclusions
This study shows that ethephon affects PN in both high and low photosynthetic capacity cultivars, Varuna and RH30. In both the cultivars, changes in PN were due to stomatal and mesophyll effects. Ethephon-induced PN was attributed to ethylene evolution. The high photosynthetic capacity cultivar, Varuna responded less to ethephon than the low photosynthetic capacity cultivar, RH30. The low PN of RH30 was due to low level of ethylene. The low photosynthetic capacity of RH30 could be enhanced to give higher PN through increase in ethylene evolution. However, for both the cultivars there is a range of physiologically active concentration of ethylene beyond which it exerts inhibitory effects.
Methods
Two cultivars of mustard (Brassica juncea L. Czern & Coss.), namely Varuna (high photosynthetic capacity) and RH30 (low photosynthetic capacity) were grown from seeds in 10 m2 field plots in complete randomized design with five replications. At seedling establishment a plant population of 12 plants m-2 was maintained and recommended plant cultivation procedures were adopted. A uniform recommended soil application of 18 g N, 3 g P and 3 g K m-2 was given at the time of sowing so as the nutrients were non-limiting.
At 30 d after sowing, 0, 0.75, 1.5 and 3.0 mM ethephon (2-chloroethyl phosphonic acid) was sprayed with a hand sprayer. Ethephon is a direct ethylene source when applied to plants and elicits response identical to those induced by ethylene gas 2324. Since ethephon on hydrolysis releases ethylene and phosphorus, therefore equivalent amount of phosphorus present in 3.0 mM ethephon was given to all treatments including control to nullify the effects of phosphorus.
At 45 d after sowing (15 d after ethephon treatment) PN, gS, Ci, CA activity, ACS activity and ethylene evolution were determined.
Measurement of photosynthetic parameters
PN, gS and Ci were measured using infrared gas analyzer (LiCOR 6200, Lincoln, NE) on fully expanded upper most leaves at saturating light intensity on four plants from each replicate. The atmospheric conditions during the experiment between 1100–1200 h were: photosynthetic active radiation about 1050 μmol m-2 s-1, relative humidity 64% and temperature 23°C, atmospheric CO2 concentration 360 μmol mol-1.
Measurement of carbonic anhydrase activity
The leaves used for photosynthesis measurement were selected for CA activity determination. CA was measured by the method of Dwivedi and Randhava 25. Leaves were cut into small pieces in 10 mL of 0.2 M cystein at 4°C. The solution adhering to the leaf surface was removed and immediately transferred to a tube having 4 mL phosphate buffer (pH 6.8). A 4 mL of 0.2 M sodium bicarbonate in 0.002 M sodium hydroxide and 0.2 mL of 0.002% bromothymol blue was added to the tube. The tubes were kept at 4°C for 20 min after shaking. Liberated CO2 during the catalytic action of enzyme on sodium bicarbonate was estimated by titrating the reaction mixture against 0.05 N hydrochloric acid.
Measurement of ACS activity and ethylene evolution
Activity of ACS was measured adopting the methods of Avni et al. 26 and Woeste et al. 27. Leaf tissue was grind in 100 mM N-2 hydroxyethylenepiperazine N-2 ethanesulfonic acid buffer (pH 8.0) containing 4 mM dithiothreitol, 2.5 mM pyridoxal phosphate and 25% polyvinylpolypyrrolidone. The preparation was homogenized and centrifuged at 12000 g for 15 min. One mL of the supernatant was placed in a 30 mL tube and 0.1 mL of 5 mM S-adenosyl methionine (AdoMet) was added. This was incubated for 1 h at 22°C. The 1-aminocyclopropane carboxylic acid formed was determined by its conversion to ethylene by the addition of 0.1 mL of 20 mM HgCl2 followed by 0.1 mL of 1:1 mixture of saturated NaOH/NaCl and incubated on ice for 10 min, and ethylene evolution was measured on a gas chromatograph. For control set AdoMet was not added. For ethylene evolution 5 mL of gas phase was removed with a syringe and ethylene was measured on a gas chromatograph (GC 5700, Nucon, New Delhi) equipped with 1.8 m Porapack N (80/100 mesh) column, a flame ionization detector and an integrator. Nitrogen was used as carrier gas. The flow rates of nitrogen, hydrogen and oxygen were 0.5, 0.5 and 5 mL s-1, respectively. The oven temperature was 100°C and detector was at 150°C. Ethylene identification was based on the retention time and quantified comparing with the peaks from standard ethylene concentrations.
Data analysis
Data were analyzed statistically and standard error of the mean value was calculated. Analysis of variance was performed to identify the significant differences among treatments at P < 0.05 28.
Abbrevations
Adomet – S-adenosyl methionine; ACS – 1-aminocyclopropane carboxylic acid synthase; CA – carbonic anhydrase; Ci – intercellular CO2 concentration; gS – stomatal conductance; PN – net photosynthetic rate