为了提高马齿苋的组培效率,解决马齿苋出愈时间迟、愈伤组织诱导率不高、愈伤组织诱导需要使用2,4-D、不定芽增殖来源有限等问题,根据马齿苋的最适生长条件,将组织培养环境调整为温度(30±1)℃、全光照,并从无菌苗上直接取材进行外植体培养。结果表明:种子在高温、全光照条件下萌发快,且无菌苗长势好。取材于无菌苗上的根、茎和叶均可以在不添加2,4-D的MS培养基中脱分化形成愈伤组织,且茎在MS+NAA 1.0 mg/L+6-BA 1.0 mg/L培养基中、叶在MS+NAA 1.5 mg/L+6-BA 0.5-1.5 mg/L培养基中的初始出愈时间均提前至4 d,且诱导率均达到100%,愈伤组织长势旺盛。带腋芽的茎段在MS+NAA 0.1 mg/L+6-BA 5.0 mg/L培养基中可以直接分化出大量不定芽,增殖率达10.5。在最适光温环境下,马齿苋外植体出愈迅速,愈伤组织诱导率和不定芽增殖率大幅度提高。
In order to improve the tissue culture efficiency of purslane,the problems,such as late callus formation, low rate of callus induction, requiring the use of 2,4-D in callus induction, and limited source of explants for adventitious buds proliferation etc. should be solved. According to the optimal growth conditions for purslane, its tissue culture environment was adjusted to(30 ±1)℃ of temperature and full light exposure, and explants were taken directly from the sterile seedlings. The results showed that seeds germinated well and aseptic seedlin gs grew fast under this condition. Callus could be induced from each organ of aseptic seedlings on MS+NAA 1.0 mg/L+6-BA 1.0 mg/L medium without the addition of2,4-D. Callus could be first found on the stems in 4 d and the callus grew very fast. After further adjust-ment for hormones,callus could be induced a hundred percent in 4 d from leaves on MS +NAA 1.5 mg/L+6-BA 0.5-1.5 mg/L medium. A large number of adventitious buds could be induced from stems with axillary buds on MS+NAA 0.1 mg/L+6-BA 5.0 mg/L medium with a proliferation rate of 10.5. Under the optimum temperature and light environment, callus from purslane explants could be induced early. The callus grew fast, and its induction rate together with proliferation rate of adventitious buds were higher.