金钱草组织培养的初步研究

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利用金钱草的茎尖做外植体,用75%酒精浸泡10s和0.2%的HgCl2处理8min,无菌水冲净后,接种于MS+2.0mg/lBA+0.5mg/lNAA培养基中建立无菌苗;将无菌苗的叶切块,接种于MS+BA0.5mg/l+NAA0.5mg/l培养基中,7d后可陆续形成绿色、质地紧密、长势好的愈伤组织;将愈伤组织移至MS+BA2.0mg/l+NAA0.2mg/l培养基中,16d后逐渐形成大量丛生芽,且长势较好;将无根苗移至1/2MS+NAA0.5mg/l或1/2MS+IBA0.5mg/l培养基中,10~12d生根,根多而且苗壮。 Explants were made from the tips of the tips of A. annua and soaked in 75% alcohol for 10s and 0.2% HgCl2 for 8 minutes. After sterilized water was rinsed, the cells were inoculated into MS + 2.0mg / lBA + 0.5mg / l NAA medium And the seedlings were inoculated with MS + BA0.5mg / l + NAA0.5mg / l medium. After 7 days, the green, compact texture and good callus could be gradually formed. Injured tissue was transferred to MS + BA2.0mg / l + NAA0.2mg / l medium, a large number of clusters of buds gradually formed after 16d, and grew well; the rootless seedlings were moved to 1 / 2MS + NAA0.5mg / l or 1 /2MS + IBA0.5mg / l medium, 10 ~ 12d rooting, more roots and strong seedlings.
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