Mondal Sananda, Bose Bandana
Department of Crop Physiology, Institute of Agriculture, Visva-Bharati, Sriniketan, 731236, India.
Department of Plant Physiology, Institute of Agricultural Sciences, Banaras Hindu University, Varanasi, 221005, India.
Biol Futur. 2024 Dec;75(4):487-496. doi: 10.1007/s42977-024-00237-z. Epub 2024 Jul 31.
This study leads with the primed seeds of rice (var. Swarna) with distilled water (D.W.) and various concentrations of Mg(NO) (0-8 mM)/Kinetin (0-5 ppm) alone or in combination with screen out the regeneration medium induced tolerance level of NaCl. To fulfill the objective, the primed and non-primed rice seeds were inoculated in MS medium supplemented with 30 gL maltose + 1 gL casein hydrolysate and 2 mgL of 2,4-D for callus induction and cultured up to 45 days in two sets: one set for regeneration purpose in NaCl-induced regeneration medium and another set was used to study the physiological potentiality of the callus. The 45-day-old calli were transferred into regeneration medium MSR (MS medium for regeneration) (BAP: NAA: Kinetin = 4:1:1) containing NaCl with a concentration range of 0 to 300 mM. The number of regenerating calli and shoot regeneration percentage, number of plantlets obtained from one callus, recovery of plantlets from each concentration of NaCl and proline estimation from the leaf of the regenerated plantlets were determined from one set obtained after 45 days. The calli obtained from another set after 45 days, the frequencies of total and embryogenic calli induction percentage, fresh and dry weights, proline content, nitrate reductase and superoxide dismutase activities were measured. The calli obtained from 2.5 ppm kinetin + 4 mM Mg(NO) primed seeds were showed best result as compared to the other treatments for the above-mentioned parameters in different concentrations of NaCl-induced medium and survive up to 200 mM concentrations of NaCl.
本研究以蒸馏水(D.W.)以及单独或组合使用的不同浓度的Mg(NO)(0 - 8 mM)/激动素(0 - 5 ppm)对水稻(品种Swarna)的引发种子进行处理,以筛选出诱导耐NaCl再生培养基。为实现该目标,将引发和未引发的水稻种子接种于添加了30 g/L麦芽糖 + 1 g/L水解酪蛋白和2 mg/L 2,4 - D的MS培养基中进行愈伤组织诱导,并分为两组培养45天:一组用于在NaCl诱导的再生培养基中进行再生,另一组用于研究愈伤组织的生理潜力。将45天大的愈伤组织转移至含有浓度范围为0至300 mM NaCl的再生培养基MSR(用于再生的MS培养基)(BAP:NAA:激动素 = 4:1:1)中。从45天后获得的一组中测定再生愈伤组织的数量和芽再生率、从一个愈伤组织获得的植株数量、每种NaCl浓度下植株的回收率以及再生植株叶片中的脯氨酸含量。测定45天后从另一组获得的愈伤组织的总愈伤组织和胚性愈伤组织诱导率、鲜重和干重、脯氨酸含量、硝酸还原酶和超氧化物歧化酶活性。与不同浓度NaCl诱导培养基中上述参数的其他处理相比,由2.5 ppm激动素 + 4 mM Mg(NO)引发种子获得的愈伤组织表现出最佳结果,并且在高达200 mM浓度的NaCl中存活。