Cumulative effect of gibberellic acid and phosphorus on crop productivity, biochemical activities and trigonelline production in Trigonella foenum-graecum L.

Abstract Fenugreek (Trigonella foenum-graecum L.) is an antidiabetic plant. Its bioactive compound, trigonelline, is known to counter diabetes through insulin secretion, modulation of β cell regeneration and quick activity of glucose metabolism related enzymes. A pot experiment was conducted in the natural conditions of net house of the Department of Botany, Aligarh Muslim University, Aligarh (UP), India, to evaluate the effect of four concentrations of GA3 (0, 10−7 M, 10−6 M and 10−5 M), alone and in combination with phosphorus (40 kg P ha−1), on growth, biochemical and yield attributes of fenugreek. Compared to control, the combination of GA3 and phosphorus (P40 + 10−6 M GA3) significantly increased the activities of nitrate reductase (30.8%) and carbonic anhydrase (30.7%) enzymes; it also enhanced the seed yield (140.6%) and the content of total chlorophyll (28.5%) and carotenoids (26%). There was also significant increase (19.51%) in the content of seed trigonelline.


ABOUT THE AUTHORS
Our research group deals with Plant Physiology and Biochemistry with a thrust on the study "Effect of plant growth regulators, mineral nutrients, nanoparticles and marine polysaccharides on growth, physiology and secondary metabolite production of medicinal and aromatic plants".
The present work shows that the combined application of gibberellic acid and phosphorus significantly enhanced the growth, physiological activities and trigonelline production in Trigonella foenum-graecum L. Further research is needed to find how GA 3 acts at molecular level to increase the production of trigonelline in this plant.

PUBLIC INTEREST STATEMENT
Trigonella foenum-graecum L., commonly known as fenugreek, is an annual herb belonging to the family Leguminosae. It is used as an antidiabetic plant. It contains bioactive compounds as trigonelline, diosgenin, 4-hydroxyisoleucine (4-HI), galactomannan flavonoids, carotenoids, coumarins, saponins and lipids. Diosgenin is used by pharmaceutical and nutraceutical industries as a precursor for the production of steroidal drugs and hormones such as testosterone, progesterone and glucocorticoids. Diabetic patients are recommended to take fenugreek as a vegetable in diet. Being such an immense medicinal plant, there is a need to enhance the growth and active constituents of this plant. Gibberellic acid (GA 3 ) is a plant growth hormone (C 19 H 22 O 6 ) that regulates seed germination, stem elongation, leaf expansion, fruit development, flowering and stimulation of secondary metabolite production in plants. In the present study, the foliar application of GA 3 in combination with soil applied phosphorus enhanced growth, biochemical attributes and yield of fenugreek. It significantly enhanced the trigonelline production as well.

Introduction
Diabetes mellitus is one of the most common diseases in the present day world with 150 million of diabetics worldwide and the number is unfortunately likely to increase to 300 million by 2025 (Shaw, Sicree, & Zimmet, 2010). For centuries, mankind has been using the medicinal plants to overcome numerous diseases and according to World Health Organization, 80% of the people in developing countries get through traditional medicines. Trigonella foenum-graecum L., commonly known as fenugreek, is one such medicinal plant that has been comprehensively used as a source of antidiabetic compounds, from its leaves, seeds and extracts in different model systems (Khalki, M'hamed, Bennis, Chait, & Sokar, 2010;Srinivasan, 2006). In India, fenugreek is mostly used in Unani and Ayurvedic therapeutic systems (Srinivasan, 2006). The important constituents of fenugreek include 4-hydroxyisoleucine (4-HI), trigonelline, galactomannan flavonoids, carotenoids, coumarins, proteins, saponins and lipids (Basch, Ulbricht, Kuo, Szapary, & Smith, 2003). Trigonelline controls the diabetes through operation of the mechanism of insulin secretion, modulation of β cell regeneration and stimulation of activity of glucose metabolism-related enzymes (Abd El-Mawla & Osman, 2011;Zhou, Chan, & Zhou, 2012). The seeds of fenugreek contain about 50% of fibre that is known to slow the rate of post-parandial glucose absorption, which may be responsible for the hypoglycaemic activity. The seed extract of fenugreek stimulates the secretion of insulin from pancreatic cells and inhibits the activities of α-amylase and sucrose (Amin, Abdul Ghani, & Suleiman, 1988). Fenugreek seeds have sapogenins which are known to lower serum cholesterol level in humans (Yadav, Moorthy, & Baquer, 2004. Gibberellins (GAs) constitute a group of tetracyclic diterpenoids, involved in plant growth and development. Gibberellic acid (GA 3 ), (Figure 1) a well known phytohormone, has numerous physiological effects on plants including seed germination, growth, stem elongation, leaf expansion, photosynthesis, flowering and cell expansion (Taiz & Zeiger, 2010;Yuan & Xu, 2001). Exogenous application of GA 3 to plants causes the increase in the activities of many key enzymes like carbonic anhydrase (CA), nitrate reductase (NR) (Afroz, Mohammad, Hayat, & Siddiqui, 2005;Aftab et al. 2010) and ribulose-1, 5-biphosphate carboxylase/oxygenase (RuBPCO) (Yuan & Xu, 2001). Phosphorus (P) is the second growth-limiting nutrient after nitrogen (Moinuddin et al., 2014) and is an integral constituent of biological macromolecules such as that of nucleic acids, phospholipids and ATP. Consequently, plants cannot grow successfully without a reliable supply of this nutrient. There may be large quantities of phosphorus present in the soil but its amount, available to plants, is generally low because of the insoluble forms of soil phosphorus. For that reason, phosphate fertilizers are added to the soil to overcome the phosphorus deficiency. In fact, there is significant gap in the knowledge regarding phosphorus nutrition of crops in Indian cropping systems. We also need to fill the gaps in our knowledge about how crops respond to phosphorus in different situations and how can phosphorus efficiency be improved supplying adequate P for crop productivity.
The present study was conducted to investigate the effect of foliar application of GA 3 alone and in combination with the soil applied P on the crop productivity, physiological and biochemical parameters, and trigonelline yield of T. foenum-graecum L.

Plant material, chemicals and growth conditions
Gibberellic acid (GA 3 ) was purchased from Duchefa Biochemie B.V, The Netherlands (Product Number: G0907; CAS Number 77-06-5) and Trigonelline hydrochloride was brought from Sigma Aldrich (Product Number: T5509; CAS Number 6138-41-6). The seeds of T. foenum-graecum L. were purchased from National Seed Corporation Unit, Indian Agricultural Research Institute (IARI), New Delhi, India. Healthy seeds of T. foenum-graecum L. were initially surface sterilized with 80% ethyl alcohol for 5 min and then washed thoroughly with double distilled water before sowing. Each experimental pot carried 5 kg homogenous mixture of soil and farmyard manure (4:1). The soil samples were tested at Soil Testing Laboratory, IARI, New Delhi, India. The experimental soil was sandy loam with pH (1:2) 7.94, E.C (1:2) 0.57 mmhos/cm, and available N, P and K 98.45, 7.15 and 141.8 mg kg −1 soil, respectively.

Experimental design and pot culture
The pot experiment was conducted at the Botany Department, Aligarh Muslim University, Aligarh, India (27° 52′ N latitude, 78° 51′ E longitude, and 187.45 m altitude) in order to ascertain the changes mediated by GA 3 and P, applied alone or in combination, on physiological and biochemical parameters as well as on growth, yield and quality attributes of T. foenum-graecum L. The experiment was conducted according to simple randomized design in the natural conditions of Net house using earthen pots (25 cm diameter × 25 cm height). Deionised water (DIW) was used as the control. Four levels of GA 3 , viz. 0 M (DIW), 10 −7 M GA 3 , 10 −6 M GA 3 and 10 −5 M GA 3 ] were employed as foliar spray treatments. Two P levels, viz. 0 (P0) and 40 kg P ha −1 (P40), were applied to the soil in the form of KH 2 PO 4 . Four concentrations of GA 3 and two levels of P were employed to constitute eight treatments [(I) Control (DIW), (II) 10 −7 M GA 3 (III) 10 −6 M GA 3 (IV) 10 −5 M GA 3 (V) 40 kg P ha −1 (P40) (VI) P40 + 10 −7 GA 3 (VII) P40 + 10 −6 GA 3 (VIII) P40 + 10 −5 GA 3 ]. In about 90% of the seeds, the germination took place within 5-6 days of sowing. After a month of germination, the number of seedlings was maintained to five per pot. Totally, 40 pots were employed for the experiment. Seeds were sown at a depth of 2 cm. Each treatment was replicated five times. Totally, six spray treatments were given at 7 days interval, using a hand sprayer, the first foliar spray treatment being applied at 30 days after sowing (DAS). The pots were watered and made weedsfree as and when required.

Determination of growth and yield attributes
Growth attributes of the T. foenum-graecum L. were determined at 60 and 90 DAS. At the respective sampling stage, five plants from each treatment (one plant from each replicate) were carefully harvested with the roots and washed with running tap water to remove adhering foreign particles. Water adhering to the roots was removed with blotting paper. Fresh weight of the clean and blotdried plants was recorded using an electronic balance. Thereafter, the plants were oven-dried at 80°C for 24 h. Dry weight of plants was recorded subsequently. The shoot and root length of the plants was measured with the help of a metre scale. Number of leaves was counted and leaf area was measured by the graph paper method. Yield parameters were noted at the time of harvesting. From each pot, the plants were harvested above ground to measure the different yield attributes, viz. seed yield and total biomass per plant, harvest index, 1,000-seed weight, number of pods per plant, number of seeds per plant, number of seeds per pod and pod length. The harvest index was calculated as (seed yield/total biomass) × 100.

Total chlorophyll and carotenoids contents
Contents of total chlorophyll and carotenoids were estimated on fresh weight basis by the method of Mac Kinney (1941) and Maclachlan and Zalik (1963), respectively. Fresh tissue from interveinal leaf areas was grinded with mortar-pestle using 80% acetone. The optical density (OD) of the solution was recorded at 645 and 663 nm for chlorophyll estimation and at 480 and 510 nm for carotenoids estimation employing a spectrophotometer (Spectronic UV-1700, Shimadzu, Japan). Concentrations of chlorophyll and carotenoids were expressed as mg g −1 FW.

Determination of NR activity
NR activity was estimated by the intact tissue assay method developed by Jaworski (1971), which is based on the reduction of nitrate to nitrite according to the following biochemical reaction: The amount of nitrite (NO 2 − ) formed was determined spectrophotometrically. Interveinal area of fresh chopped leaves, weighing 0.2 g, was transferred to each of the plastic vials. Reaction mixture of each vial was comprised of 2.5 mL phosphate buffer (pH 7.5), 0.5 mL of potassium nitrate solution and 2.5 mL of 5% isopropanol solution. The vials, carrying the reaction mixture, were kept in an incubator maintained at 30°C for the manifestation of maximum enzyme activity. After the incubation period (2 h), 0.4 mL of the content was transferred to a test tube. To it, 0.3 mL each of 1% sulphanilamide and 0.02% N-(1-Naphthyl) ethylenediamine dihydrochloride (NED-HCl) was added. The test tubes were kept for 20 min at room temperature for maximum colour development. The OD of the content was recorded at 540 nm using the spectrophotometer. The NR activity was expressed as nanomoles of nitrite produced per gram fresh weight of the leaf tissue per hour (nM NO 2 − g −1 FW h −1 ).

Determination of CA activity
CA activity was analysed in fresh leaves using the method as described by Dwivedi and Randhawa (1974). Two hundred milligram (0.2 g) of fresh interveinal leaf tissue was transferred to Petri plate, followed by its incubation in 10 mL of 0.2 M cystein hydrochloride solution for 20 min at 4°C. Thereafter, 4 mL of 0.2 M sodium bicarbonate solution and 0.2 mL of 0.02% bromothymol blue was added to the homogenate. The reaction mixture was titrated against 0.05 N HCl using methyl red as indicator. The activity of CA was expressed as moles of CO 2 produced per kg of fresh leaf tissue per second (mM CO 2 kg −1 leaf FW s −1 ).

Estimation of N, P and K contents in leaves
Leaf samples from each treatment were digested for the estimation of leaf-N, -P and -K contents. The leaves were dried in a hot-air oven maintained at 80°C for 24 h. Dried leaves were powdered using mortar-pestle, followed by passing the powder through a 72 mesh. The sieved leaf powder was used for the estimation of N, P and K contents. One hundred mg of oven-dried leaf powder was carefully transferred to a digestion tube, to which 2 mL of concentrated sulphuric acid (analytical grade) was added subsequently. The content was heated for about two hours on a temperaturecontrolled digestion assembly maintained at 80°C; and then, the content was cooled at room temperature for about 15 min. To the cooled content, 0.5 mL of 30% hydrogen peroxide (H 2 O 2 ) was added drop by drop. The addition of H 2 O 2 was followed by gentle heating of the content and then cooling at room temperature. This step was repeated until the content of the tube turned colourless. The aliquot (peroxide-digested leaf material), thus prepared, was used to estimate the percentage of N, P and K contents in the leaves on dry weight basis.

Determination of leaf-N content:
Leaf-N content was estimated according to method of Lindner (1944) with slight modification by Novozamsky, Houba, van Eck, and van Vark (1983). A 10 mL aliquot (peroxide digested leaf material) was poured into a 50 mL volumetric flask. To it, 2 mL of 2.5 N sodium hydroxide solution and 1 mL of 10% sodium silicate solution was added to neutralize the excess acid and prevent turbidity, respectively. A 5 mL aliquot of the peroxide digested material was poured into a 10 mL graduated test tube, followed by addition of 0.5 mL of Nessler's reagent. The OD of the solution, thus obtained, was recorded at 525 nm using the spectrophotometer.

Determination of leaf-P content:
The method of Fiske and Subba Row (1925), with slight modification by Rorison, Spencer, and Gupta (1993), was used to estimate the leaf-P content. A 5 mL aliquot of the peroxide-digested leaf material was poured into a 10 mL graduated test tube. To it, 1 mL of molybdic acid (2.5%) was added, followed by addition of 0.4 mL of 1-amino-2-naphthol-4sulphonic acid. When the colour of the content turned blue, its volume was made up to 10 mL usingdouble distilled water. The OD of the solution, thus obtained, was recorded at 620 nm using the spectrophotometer.

Determination of leaf-K content:
Leaf-P content was determined using a flame photometer (Model, C150, AIMIL, India) with the help of emission spectra using specific filter. In the flame photometer, the solution (peroxide-digested leaf material) was discharged through an atomizer in the form of a fine mist into a chamber, where it was drawn into a flame. Combustion of the solution elements produced the light of a particular wavelength [k max for K = 767 nm (violet)]. The light, thus produced, was passed through an appropriate filter to impinge upon a photoelectric cell that subsequently activated a galvanometer (electric current detector).

Seed alkaloid content
To estimate total seed alkaloid content, 1 g of seed powder was ground with 80% methanol and a pinch of magnesium oxide (MgO), using mortar-pestle. The sample was incubated at 60°C for about 30 min; the homogenate was centrifuged, followed by collecting the supernatant. Methanol was evaporated completely and the residue was dried. Thereafter, the weight of the beaker containing the residue and that of the empty beaker was recorded.
Total seed alkaloid content (%) was calculated using following formula: where WE is the Weight of empty beaker (g); WA is the Weight of porcelain dish after evaporation (g); and WR is the Weight of the seed powder (g).

Extraction and estimation of trigonelline by high performance liquid chromatography
To extract seed trigonelline content of T. foenum-graecum L., the method of Zheng and Ashihara (2004) was adopted with a slight modification. One gram of seed powder was grinded with 80% methanol with a pinch of magnesium oxide (MgO) using mortar-pestle. The sample was incubated at 60°C for about 30 min, the homogenate was centrifuged, followed by collecting the supernatant. Methanol was evaporated and the extract was dissolved in distilled water. The content was filtered using disposable syringe filter unit and stored thereafter in sealed vials for the determination of trigonelline by high performance liquid chromatography (HPLC). Seed trigonelline content was determined by isocratic HPLC equipment (Model, LC-20AD, Shimadzu Corporation Analytical & (WA − WE∕WR) × 100 Measuring Instrument Division, Kyoto, Japan) with reverse phase C-18 (5 μm, 150 mm, 4.6 mm I.D,) column. Mobile phase consisted of methanol and water in the ratio of 50:50 (v/v) and the pH was adjusted to 5 using acetic acid. The elution was made in an isocratic mode at the flow rate of 1 mL min −1 and the detection was made at 268 nm by UV-vis detector. Calibration curve was made by using graded concentrations (0, 50, 100, 150 and 200 mg L −1 ) of standard trigonelline hydrochloride (Sigma Aldrich, USA), (Figure 2) with the help of HPLC equipment.

Statistical data analysis
The data were analysed statistically using SPSS-17 statistical software (SPSS Inc., Chicago, IL, USA) according to randomized design. Means were compared applying the Fisher's least significant difference (LSD) test at p < 0.05.

Results
Among different concentrations of gibberellic acid, 10 −6 M GA 3 proved to be the best for most of the parameters studied. GA 3 , applied in combination with phosphorus (i.e. P 40 + 10 −6 M GA 3 ) proved to be the best treatment for almost all of the parameters studied. This treatment was followed by P 40 + 10 −7 M GA 3 . The spray treatment of DIW (control) resulted in the lowest values (Tables 1 and 2; Figures 3 and 4).

Growth attributes
Foliar application of GA 3 progressively improved the growth attributes of fenugreek both at 60 and 90 DAS ( Table 1). The highest values of growth parameters were attained at 90 DAS with the combination treatment, i.e. P 40 + 10 −6 M GA 3 . In comparison to the control, P 40 + 10 −6 M GA 3 increased the shoot length by 41 and 44%, root length by 31.33 and 45.19%, leaf number by 33.32 and 43.24%, leaf area by 33.26 and 32.43%, shoot fresh mass by 41.46 and 39.96%, root fresh mass by 37.65 and 39.95%, shoot dry mass by 46.73 and 42.45%, root dry mass by 36.59 and 40% at 60 and 90 DAS, respectively (Table 1).

Photosynthetic pigments
Gibberellic acid treatment increased the total chlorophyll and carotenoids content in the treated plants significantly. Of all the GA 3 concentrations applied alone, 10 −6 M GA 3 proved to be the best. However, among combinations, P 40 + 10 −6 M GA 3 gave the best results. In comparison to the control,

NR activity
Treatment combination P 40 + 10 −6 M GA 3 increased the NR activity to the highest extent, increasing the leaf NR activity by 27.91 and 30.88% at 60 and 90 DAS, respectively.

CA activity
In the present investigation, CA activity was found to be improved over the control as a result of phosphorus application along with 10 −6 M GA 3 . In the present study, P 40 + 10 −6 M GA 3 exhibited greater CA activity than those sprayed with deionized water (control) to the extent of 28.13 and 30.77% at 60 and 90 DAS, respectively.

Discussion
Very few studies have been carried out to investigate the effect of gibberellic acid (GA 3 ) on fenugreek. Besides, no work has till date been cited exploring the effect of GA 3 and P combination on fenugreek, which is an antidiabetic plant. Hence, it might be considered as the first report of its kind, revealing the combined effect of GA 3 and P on growth and other physiological attributes, yield and bioactive constituents of fenugreek. Plant growth and development is known to be governed by several exogenous and endogenous factors, including the growth regulators (Taiz & Zeiger, 2010). In the present investigation, the significant increase in the shoot and root length, fresh and dry weight, number of leaves and leaf area might be ascribed to the well known effects of GA 3 and P in plants. It is a recognized fact that GA 3 promotes cell enlargement and cell division (Buchanan, Gruissem, & Jones, 2000;Taiz & Zeiger, 2010). The studies conducted by Srivastava and Srivastava (2007) also support the fact that foliar application of GA 3 could increase the plant height and leaf length in Catharanthus roseus. Increase in growth parameters in the plants treated with GA 3 might be ascribed to the induction of inherent genetic potential of the plant by exogenous application of PGRs, which might cause increase in elongation of internodes as a result of cell division and cell wall extensibility (Khan et al., 2006;Taiz & Zeiger, 2010). In the present study, GA 3 increased the leaf area of fenugreek; similar results were obtained regarding Saccharum officinarum (Dhaliwal, Malik, Gosal, & Dhaliwal, 1997) and several field grown plants (Zhou, MacKenzie, Madramootoo, & Smith, 1999) on account of GA 3 application. Growth promotion by the exogenous application of GA 3 is also reported in C. roseus (Srivastava & Srivastava, 2007) and Nigella sativa (Shah, Ahmad, & Samiullah, 2006). In view of the essential role of phosphorus in plant growth and development (Marschner, 2002), the increment in plant fresh and dry mass could be expected as a result of soil-applied phosphorus (Table 1). In the present study, the interactive effect of P and GA 3 resulted into the best values of growth parameters. The beneficial effects of phosphorus on growth of plants have been reported with regard to different medicinal plants (Chaudhary et al., 2009;Dutta & Bandyopadhyay, 2009;Naeem, Khan, & Mohammad, 2009;Naeem, Masroor, & Khan, 2009).
As per the present study, massive improvement (28.57 and 26%) was found in chlorophyll and carotenoids content when P and GA 3 were applied together (Figure 3). The increased contents of chlorophyll and carotenoids could, possibly, be attributed to the enhancement of ultrastructural morphogenesis of plastids by GA 3 as suggested by Arteca (1996). Our results are in agreement with other studies conducted by different workers in different plants like Zea mays (Sinha, Srinivatsa, & Tripathi, 1993), Glycine max (Zhao, Lin, Shi, & Chang, 1995) and Schefflera arboricola L. (Salehi Sardoei, Roein, Shahadadi, Sadeghi, & Mokhtari, 2014). The enhancement of the photosynthetic pigments due to P application has earlier been reported by     and Naeem, Masroor, et al. (2009).
CA is one of the most abundant zinc containing proteins in plants. It catalyzes the reversible hydration of CO 2 to carbonic acid, thereby increasing the availability of CO 2 to RuBisCO in photosynthesis (Khan, Javed, & Samiullah, 2004). An increase in CA activity in this study could be ascribed to the ample accessibility of phosphorus at the site of its metabolism. A probable reason for the enhancement of CA activity by the foliar application of GA 3 alone or in combination with soil-applied P might be the de nova synthesis of CA which might involve translation/transcription of respective genes (Okabe, Angela, Mikio, & Shigetoh, 1980). Furthermore, the enhanced activity of CA in the treated plants might have increased the CO 2 fixation, which ultimately might be responsible for the increase in fresh and dry mass of treated plants (Table 1).
NR is known to be a rate-limiting enzyme in nitrogen assimilation and its level depends on a variety of factors, either external or internal. The activity of this enzyme in plants gives a good approximation of the nitrogen eminence of the plant and is very often correlated with growth, yield and protein synthesis. One of the reasons of GA 3 -enhanced NR activity in this study might be the GA 3 -improved leaf nitrogen content that might have increased the concentration of nitrate in the leaves to be acted upon by NR (Figure 4). Above all, P 40 + 10 −6 M GA 3 treatment proved to be the best and increased the NR activity by 30.88% over the control. Phosphorus application has resulted in increased NR activity in other plants like Zea mays (de Magalhães et al., 1998) and Phaseolus vulgaris (Gniazdowska, Krawczak, Mikulska, & Rychter, 1999), which confirmed the enhanced assimilation of leaf NO 3 − content due to P application. Besides, enhancement in leaf NR activity with phosphorus application has also been reported in different medicinal and aromatic plants such as Cassia tora (Naeem & Khan, 2005), Cyamopsis tetragonoloba L. (Burman, Kumar Garg, & Kathju, 2007) and Senna occidentalis L. ).
Foliar application of GA 3 alone and in combination with soil-applied P proved effective for N, P and K contents in fenugreek (Figure 4). The concentration of leaf nutrients (N, P and K) was significantly greater in plants treated with P 40 + 10 −6 M GA 3 as compared to the control. According to Al Wakeel, Hamed, and Dadoura (1995) application of GA 3 increased the root membrane permeability, which might ultimately facilitate the absorption, transport and utilization of mineral nutrient in plants as argued by Khan, Ansari, and Samiullah (1998) in the case of Brassica juncea. Moreover, the plants treated with GA 3 had more biomass as reflected from the shoot and root dry mass of the plants (Table 1). The enhancement in plant biomass in the present investigation could presumably be as a result of increased uptake of nutrients, enhanced photosynthesis and improved translocation of photosynthates and other metabolites to the reproductive parts as suggested by Miniraj and Shanmugavelu (1987) regarding Capsicum annum. As per Figure 4, the enhancement in leaf-N, -P and -K content could be due to phosphorus-encouraged absorption of additional amount of nutrients from the soil as noted by Graciano, Goya, Frangi, and Guiamet (2006) with regard to Eucalyptus grandis. Our results in this regard are consistent with those of earlier studies on different medicinal crops (Khan, Samiullah, Afaq, & Afridi, 2000;Naeem & Khan, 2005Naeem, Masroor, et al. (2009). GA 3 application improved the seed yield in fenugreek (Table 2). Such an observation has been made in other plants also like Zea mays (Naghashzadeh, 2007) and Glycine max (Azizi, Moradii, Heidari, Khalili, & Feizian, 2012). The increase in seed yield due to GA 3 might be accounted for its possible positive effects on 1,000 seed weight, pod set, increased CO 2 fixation and increase in leaf area. Besides, the enhanced values of yield parameters with phosphorus might be because of its important role in root and shoot development, energy translocation and other metabolic processes of plants (Marschner, 2002). In fact, the adequate amount of phosphorus in the early plant growth causes rapid cell division and cell elongation in the meristematic regions, leading to enhanced development of seeds and increased seed yield (Spencer & Chan, 1991;Turk, Tawaha, & Samara, 2003). The increase in seed yield ultimately might cause the increase in the yield of trigonelline. Trigonelline (N-methylnicotinic acid) is derived from nicotinic acid and the reaction is catalyzed by S-adenosyl-L-methionine (SAM)-dependent nicotinate enzyme N-methyltransferase. The positive effect of GA 3 on trigonelline content could be attributed to the improved plant growth and metabolism as observed in our study (Tables 1 and 2; Figures 3 and 4). Srivastava and Srivastava (2007) claimed that GA 3 enhanced the accumulation of secondary metabolites like steroids, terpenoid and anthocyanin production. In addition, GA 3 improved the accumulation of steroidal alkaloids in