Firoozabady E, Gutterson N
DNA Plant Technology Corporation, CA 94608, Oakland, USA.
Plant Cell Rep. 2003 Jun;21(9):844-50. doi: 10.1007/s00299-003-0577-x. Epub 2003 Apr 11.
We have developed an efficient and cost-effective method for commercial micropropagation of Smooth Cayenne pineapple. In vitro shoots were used as starting materials, and either longitudinal sections of the shoots or leaf bases were used as the explants to regenerate shoots. When these explants were used, the axillary meristems, which usually remain quiescent during shoot multiplication, were able to form new shoots. Subsequent to the regeneration step, additional multiplication was achieved inside a 10-l Nalgene vessel with shoots immersed in liquid medium for 5-10 min/h (periodic immersion bioreactor, PIB). The shoots were then induced to form roots and transferred to soil. Using the above micropropagation method and the PIB, we produced 6,000-8,000 shoots from two initial shoots in less than 6 months. The clonal fidelity of propagated plants was tested in Costa Rican and Indonesian pineapple farms.
我们已经开发出一种高效且经济高效的方法用于卡因类菠萝的商业化微繁殖。以离体芽作为起始材料,将芽的纵切片或叶基部用作外植体来再生芽。当使用这些外植体时,通常在芽增殖过程中保持静止的腋生分生组织能够形成新的芽。在再生步骤之后,在一个10升的耐洁容器中实现额外的增殖,将芽浸入液体培养基中5 - 10分钟/小时(周期性浸没生物反应器,PIB)。然后诱导芽生根并转移到土壤中。使用上述微繁殖方法和PIB,我们在不到6个月的时间里从两个初始芽中培育出了6000 - 8000个芽。在哥斯达黎加和印度尼西亚的菠萝农场对繁殖植物的克隆保真度进行了测试。