ABSTRACT
Aims: To develop Sequence Characterized Amplified Region (SCAR) marker for identification of Bacopa monnieri (L.) Wettst. Study design: Molecular biology tools for authentic identification of Bacopa monnieri. Methodology: RAPD-based SCAR marker was developed to identify Bacopa monnieri from its adulterant candidates namely Centella asiatica, Eclipta alba and Malva rotundifolia. 50 random primers were used for initial screening of different accessions of Bacopa monnieri, Eclipta alba and Malva rotundifolia. A putative 589 bp marker specific to Bacopa monnieri was identified using RAPD technique. This RAPD-amplicon was then sequenced and cloned. Based on the information of cloned sequences a pair of SCAR primers was designed. SCAR primers were then used for authentication of DNA samples of Bacopa monnieri and its adulterants. Market samples of Bacopa monnieri and Centella asiatica collected under the name of Brahmi was put to test with these primers. Results: Out of 50 random primers, only 14 primers were able to amplify the above plants. A 589 bp polymorphic band obtained with OPAA-3 primer which was specific to Bacopa monnieri accessions and not found in other adulterant candidates was selected. This band was eluted, cloned and further sequenced. A pair of SCAR primers (Bac F & Bac R) between 406 bp of 589 bp sequence of RAPD amplicon was designed. A single, bright, distinct band was obtained in Bacopa monnieri and not in the adulterants. Further validation was also done in the market samples. Conclusion: In essence, the study was to develop a RAPD-based SCAR marker for authentication of Bacopa monnieri. The SCAR marker was found to be useful for preventing the adulteration of other plants in Brahmi and also for screening of crude drug samples intended for export and domestic uses.
ABSTRACT
Contamination of soil and water by chromium (Cr) is increasing enormously due to anthropogenic activities. The potential of plants to accumulate or stabilize Cr compounds for the purpose of remediation of Cr contamination has been recognized in recent years. We conducted pot experiments to study photosynthesis and associated attributes in cv Pusa Jai Kisan of Indian mustard under natural as well as Cr-loaded environmental conditions. High doses of Cr caused toxic effects in plants, as evident by a reduction in photosynthetic rate (24.3 to 8.7 Cmol CO2 m-2 s-1 at 80 DAS), nitrate reductase activity (3.76 to 1.30 Cmol nitrite g-1 f. wt. h-1 at 80 DAS) and the contents of chlorophyll (1.49 to 0.86 mg g-1 f. wt. at 80 DAS) and soluble protein (2.96 to 1.93 mg g-1 f. wt. at 80 DAS). Since plants lack a specific Cr-transport system, mineral nutrient contents also changed due to Cr toxicity. Cr accumulation in different plant parts was affected by both duration and dose of Cr treatments, with a maximal localization of Cr in roots (up to 0.77 mg g-1 d. wt) at initial stages (40 DAS) and in stem (up to 4.19 mg g-1 d. wt) at the later stage (80 DAS) of plant growth. Thus, Indian mustard was able to withstand Cr stress and protect itself from Cr toxicity by altering various metabolic processes. Owing to its ability to accumulate large amounts of Cr, it may be useful in the process of land reclamation.
ABSTRACT
Plant biomass, antioxidant enzymes activity, ions accumulation and proline level in four soybean cultivars were investigated at different NaCl concentrations (20, 40, 60, 80 and 100 mM) applied to plants 15 days after sowing. There was a significant decrease in plant biomass and soluble protein content with each NaCl treatment. Accumulation of Na+ and Cl– was maximum in roots, followed by the stem and leaves in all the treated cultivars; Pusa 9712 being the top accumulator. On the contrary, K+ and Ca2+ ion concentrations were inhibited in all the treated cultivars. Activities of antioxidant enzymes (superoxide dismutase, ascorbate peroxidase and glutathione reductase) and proline content increased significantly in all the cultivars with each NaCl treatment. The maximum increase was found in Pusa 9712. However, catalase activity decreased in all the cultivars except in Pusa 9712. On the whole, Pusa 9712 was most efficient in managing protection against salinity stress.
ABSTRACT
Objective: To develop a simple, sensitive, precise, and accurate stability-indicating high performance thin-layer chromatographic method for analysis of curcumin (the main active constituent of turmeric). Methods: The separation was achieved on TLC aluminum plates precoated with silica gel 60F254 using toluene-chloroform-methanol (5:4:1, v/v/v) as a mobile phase. Densitometric analysis was performed at 430 nm. Results: This system was found to have compact spot of curcumin at RF value of (0.31±0.02). For the proposed procedure, linearity (r2= 0.99354 ± 0.00120), limit of detection (50 ng/spot), limit of quantification (200 ng/spot), recovery (ranging from 98.35% - 100.68%), and precision (≤2.25%) were found to be satisfactory. Statistical analysis reveals that the content of curcumin in different geographical region varied significantly.Conclusions:The highest and lowest concentration of curcumin in Turmeric was found to be present in sample of Erode (Tamilnadu) and Surat (Gujrat) respectively which inferred that the variety of turmeric found in Erode (Tamilnadu) is much superior to other region of India.
ABSTRACT
This study assesses the effect of NaCl (80 and 160 mM) and CaCl2 (10 mM) solutions, alone and in combination, to 30-day-old seedlings of Cichorium intybus L. Observations were made at 30 day intervals from the time of treatment till harvest (180 days after sowing). Application of NaCl resulted in significant decreases in lengths of root and stem, in dry weights of root, stem and leaves and in the leaf area, as compared with control. The reduction was less with the combined application of NaCl and CaCl2 than with the NaCl treatment alone. On the contrary, treatment of CaCl2 alone promoted the above variables. Proline content in the leaves was enhanced with NaCl and CaCl2 alone as well as with the NaCl + CaCl2 treatments; the maximum (six-fold) enhancement was observed with the combined treatments, compared with NaCl (four-fold increase) and CaCl2 (two-fold increase) alone. The sodium (Na+) and Chloride (Cl) contents in different plant parts increased both with NaCl and with NaCl + CaCl2 treatments. The maximum accumulation was observed in leaves, followed by that in stem and root. The potassium (K+) and calcium (Ca2+) contents decreased under NaCl stress, but increased with CaCl2 treatment. Thus, calcium ameliorated the deleterious effects of NaCl stress and stimulated the plant metabolism and growth.