Lee J J, Ahmad S, Roslan H A
Department of Molecular Biology, Universiti Malaysia Sarawak, 94300 Kota Samarahan, Sarawak, Malaysia.
Pak J Biol Sci. 2013 Dec 15;16(24):1913-21. doi: 10.3923/pjbs.2013.1913.1921.
Morinda citrifolia, is a valuable medicinal plant with a wide range of therapeutic properties and extensive transformation study on this plant has yet been known. Present study was conducted to establish a simple and reliable transformation protocol for M. citrifolia utilising Agrobacterium tumefaciens via direct seed exposure. In this study, the seeds were processed by tips clipping and dried and subsequently incubated in inoculation medium. Four different parameters during the incubation such as incubation period, bacterial density, temperature and binary vectors harbouring beta-glucuronidase (GUS) gene (pBI121 and pGSA1131), were tested to examine its effect on transformation efficiency. The leaves from the treated and germinated seedlings were analysed via Polymerase Chain Reaction (PCR), histochemical assay of the GUS gene and reverse transcription-PCR (RT-PCR). Results of the study showed that Agrobacterium strain LBA4404 with optical density of 1.0 and 2 h incubation period were optimum for M. citrifolia transformation. It was found that various co-cultivation temperatures tested and type of vector used did not affect the transformation efficiency. The highest transformation efficiency for M. citrifolia direct seed transformation harbouring pBI121 and pGSA1131 was determined to be 96.8% with 2 h co-cultivation treatment and 80.4% when using bacterial density of 1.0, respectively. The transformation method can be applied for future characterization study of M. citrifolia.
海巴戟是一种具有广泛治疗特性的珍贵药用植物,然而对该植物的广泛转化研究尚不为人所知。本研究旨在通过直接种子暴露利用根癌农杆菌建立一种简单可靠的海巴戟转化方案。在本研究中,种子经过剪尖和干燥处理,随后在接种培养基中培养。在培养过程中测试了四个不同参数,如培养时间、细菌密度、温度以及携带β-葡萄糖醛酸酶(GUS)基因的双元载体(pBI121和pGSA1131),以检验其对转化效率的影响。通过聚合酶链反应(PCR)、GUS基因的组织化学分析和逆转录PCR(RT-PCR)对处理过的和发芽的幼苗的叶片进行分析。研究结果表明,光密度为1.0且培养时间为2小时的根癌农杆菌菌株LBA4404最适合海巴戟的转化。结果发现,测试的各种共培养温度和使用的载体类型均不影响转化效率。携带pBI121和pGSA1131的海巴戟直接种子转化的最高转化效率在共培养处理2小时时确定为96.8%,使用细菌密度为1.0时为80.4%。该转化方法可应用于未来海巴戟的特性研究。