Pawar Kiran D, Joshi Swati P, Bhide Sunil R, Thengane Shubhada R
Plant Tissue Culture Division, National Chemical Laboratory, Pune 411008, Maharashtra, India.
J Biotechnol. 2007 Jul 15;130(4):346-53. doi: 10.1016/j.jbiotec.2007.04.024. Epub 2007 May 6.
Callus cultures of Calophyllum inophyllum were established using seed, nodal/ internodal and leaf explants on WPM basal medium supplemented with indole-3-butyric acid (IBA), alpha-naphthalene acetic acid (NAA), picloram (4-amino-3,5,6-trichloropicolinic acid), and 6-benzylaminopurine (BAP) in different combinations and concentrations with the view to study the influence of hormones on callus induction and the pattern of expression of dipyranocoumarins including anti-HIV, non-nucleoside reverse transcriptase inhibitors inophyllum B and P in callus cultures. 96.01% seed explants, 87.50% nodal/internodal explants and 86.66% leaf explants were converted into calluses when inoculated on WPM supplemented with IBA 4.0 mg l(-1) along with BAP 1.0 mg l(-1), IBA 4.0 mg l(-1), and picloram 6.0 mg l(-1) along with BAP 2.0 mg l(-1), respectively. Calluses induced from seed explants were white, friable and irregular whereas nodal/internodal and leaf explants induced dark brown, nodular and compact calluses. In order to facilitate the rapid quantitative analysis of dipyranocoumarins under study, a novel HPLC method capable of separating all six dipyranocoumarins in a single isocratic run has been optimized. Quantitative HPLC analysis of callus extracts revealed that highest inophyllum B (40.59 mg 100g callus(-1)) was expressed in callus induced from seed explant on medium containing 2.0 mg l(-1) indole-3-butyric acid, while highest inophyllum P (141.35 mg 100g callus(-1)) was estimated in seed callus induced on medium containing 2.0 mg l(-1) indole-3-butyric acid along with BAP 1.0 mg l(-1).
以红厚壳种子、节段/节间和叶片外植体为材料,在添加了吲哚 - 3 - 丁酸(IBA)、α - 萘乙酸(NAA)、毒莠定(4 - 氨基 - 3,5,6 - 三氯吡啶甲酸)和6 - 苄基腺嘌呤(BAP)的不同组合及浓度的WPM基本培养基上建立愈伤组织培养体系,旨在研究激素对愈伤组织诱导的影响以及双吡喃香豆素(包括抗HIV的非核苷类逆转录酶抑制剂红厚壳素B和P)在愈伤组织培养物中的表达模式。当分别接种在添加4.0 mg l(-1) IBA和1.0 mg l(-1) BAP、4.0 mg l(-1) IBA以及6.0 mg l(-1) 毒莠定和2.0 mg l(-1) BAP的WPM培养基上时,96.01%的种子外植体、87.50%的节段/节间外植体和86.66%的叶片外植体转化为愈伤组织。种子外植体诱导出的愈伤组织呈白色、易碎且不规则,而节段/节间和叶片外植体诱导出深褐色、结节状且紧实的愈伤组织。为便于对所研究的双吡喃香豆素进行快速定量分析,已优化了一种能够在单次等度洗脱中分离所有六种双吡喃香豆素的新型高效液相色谱法。愈伤组织提取物的高效液相色谱定量分析表明,在含有2.0 mg l(-1) 吲哚 - 3 - 丁酸的培养基上由种子外植体诱导的愈伤组织中,红厚壳素B的表达量最高(40.59 mg 100g愈伤组织(-1)),而在含有2.0 mg l(-1) 吲哚 - 3 - 丁酸和1.0 mg l(-1) BAP的培养基上诱导的种子愈伤组织中,红厚壳素P的含量最高(141.35 mg