Rajam Manchikatla V, Kumar S Vinod
Plant Polyamine and Transgenic Research Laboratory, Department of Genetics, University of Delhi - South Campus, Benito Juarez Road, New Delhi 110 021, India.
Methods Mol Biol. 2006;344:421-33. doi: 10.1385/1-59745-131-2:421.
This protocol describes the Agrobacterium tumefaciens-mediated nuclear transformation of a microalgae Chlamydomonas reinhardtii, using a gene construct carrying the genes coding for beta-glucuronidase (gus), green fluorescent protein (gfp), and hygromycin phosphotransferase (hpt). The transformation frequency with this protocol as revealed by hygromycin resistance was many fold higher (about 50-fold) than that of the commonly used glass bead method of transformation. The simplicity of Agrobacterium-mediated gene transfer and the high transformation frequency as well as the precision of T-DNA integration will enable further molecular dissection of this important model organism as well as other algal systems to understand basic plant metabolic processes as well as to exploit the systems for biotechnological applications.
本方案描述了根癌农杆菌介导的莱茵衣藻微藻核转化,使用携带编码β-葡萄糖醛酸酶(gus)、绿色荧光蛋白(gfp)和潮霉素磷酸转移酶(hpt)基因的基因构建体。通过潮霉素抗性揭示的该方案的转化频率比常用的玻璃珠转化方法高许多倍(约50倍)。根癌农杆菌介导的基因转移的简单性、高转化频率以及T-DNA整合的精确性,将有助于对这种重要的模式生物以及其他藻类系统进行进一步的分子剖析,以了解基本的植物代谢过程,并开发这些系统用于生物技术应用。