In vitro Callus Induction of Tomato and Evaluation of Antioxidant Activity of Aqueous Extracts and Enzymatic Activities in Callus Cultures

A. El-Hameid, R. Asmaa
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Abstract

Background: Tomato (Solanum lycopersicum L.) is an important plant rich in many vitamins and antioxidant enzymes. Methods: Tomato leaves of two cultivars (‘Peto 86’ and ‘Strain B’) were used as explant sources for callus induction. The antioxidant activity of the calli ethanol (ET) and methanol (ME)extracts were determined. The enzymatic activities were evaluated in callus cultures. Callus induced from leaf explants of tomato cultivars on the Murashige and Skoog (MS) medium supplemented with various concentrations and combinations of cytokinins and auxins such as BAP (6-benzylaminopurine), NAA (1-naphthalene acetic acid), 2,4-D (2,4-dichlorophenoxyacetic acid), IAA (indole-3-acetic acid) and Kin (Kinetin) for rapid induction of callus and biomass growth. Results: The medium (M2) containing 3 mg L-1 BAP with 1 mg L-1 IAA produced the highest percentage of callus induction (PCI) (100%) in two cultivars. The relative fresh weight growth (RFWG) was reported by the fresh callus weighed after four weeks of culture and again weighed after one month of sub-culture. In both cultivars cultured on M2 medium the RFWG was (1.60) in ‘Peto 86’ and (1.47) in ‘Strain B’. The results showed that PCI and RFWG differed with the cultivars tested. The scavenging DPPH free radical activity in callus (ET) extracts exhibited a significant increase in (P < 0.05) than the activity in callus (ME) extract. The peroxidase and polyphenol oxidase activities were found in calli of both tomato cultivars. The enzymatic activities were higher in callus of ‘Peto 86’ cultivar than in callus of ‘Strain B’ cultivar. Conclusions: Calli had antioxidant and enzyme activities that can be beneficial for extracting important components or for plant regeneration.
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番茄离体愈伤组织诱导及愈伤组织水提物抗氧化活性及酶活性评价
背景:番茄(Solanum lycopersicum L.)是富含多种维生素和抗氧化酶的重要植物。方法:以‘Peto 86’和‘菌株B’2个番茄品种的叶片为外植体诱导愈伤组织。测定愈伤组织乙醇(ET)和甲醇(ME)提取物的抗氧化活性。在愈伤组织培养中测定酶活性。在添加不同浓度的细胞分裂素和生长素BAP(6-苄基氨基嘌呤)、NAA(1-萘乙酸)、2,4-d(2,4-二氯苯氧乙酸)、IAA(吲哚-3-乙酸)和Kin (Kinetin)组合的Murashige和Skoog (MS)培养基上诱导番茄叶片外植体愈伤组织,快速诱导愈伤组织和生物量生长。结果:含3 mg L-1 BAP和1 mg L-1 IAA的培养基(M2)对两个品种的愈伤组织诱导率最高(100%)。相对鲜重增长(RFWG)是在培养4周后称量新鲜愈伤组织,继代培养1个月后再次称量。2个品种在M2培养基上的RFWG分别为(1.60)和(1.47)。结果表明,PCI和RFWG在不同品种间存在差异。愈伤组织(ET)提取物清除DPPH自由基的活性显著高于(P < 0.05)愈伤组织(ME)提取物。两种番茄愈伤组织均有过氧化物酶和多酚氧化酶活性。Peto 86愈伤组织的酶活性高于B菌株愈伤组织。结论:愈伤组织具有抗氧化活性和酶活性,有利于提取重要成分或促进植株再生。
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