Hall L M, Taylor K B, Jones D D
Department of Biochemistry, University of Alabama, Birmingham 35294.
Gene. 1993 Feb 14;124(1):75-81. doi: 10.1016/0378-1119(93)90763-s.
Genomic transformation of Chlamydomonas reinhardtii exposed to glass-bead abrasion was accomplished with a chimeric neomycin phosphotransferaseII (NPTII)-encoding gene (nos::npt) flanked by the nopaline synthase promoter and polyadenylation sequences obtained from the Ti plasmid of Agrobacterium tumefaciens. These sequences were in a plasmid (pGA482) which also contained gene nit1 encoding nitrate reductase of C. reinhardtii. Transformants were selected by their ability to grow on medium containing nitrate, and 52% of these was also resistant to kanamycin. Evidence for nos::npt expression includes: (1) hybridization with probes specific for npt, (2) demonstration of NPTII activity after electrophoresis of extracts, and (3) chromatographic identification of the reaction product of NPTII, kanamycin phosphate. The highly biased codon usage in Chlamydomonas does not preclude expression.
利用携带嵌合新霉素磷酸转移酶II(NPTII)编码基因(nos::npt)的质粒对经玻璃珠研磨处理的莱茵衣藻进行基因组转化,该基因两侧为来自根癌土壤杆菌Ti质粒的胭脂碱合成酶启动子和聚腺苷酸化序列。这些序列存在于质粒(pGA482)中,该质粒还包含编码莱茵衣藻硝酸还原酶的基因nit1。通过转化体在含硝酸盐培养基上的生长能力进行筛选,其中52%的转化体也对卡那霉素具有抗性。nos::npt表达的证据包括:(1)与npt特异性探针杂交;(2)提取物电泳后证明NPTII活性;(3)通过色谱法鉴定NPTII的反应产物磷酸卡那霉素。莱茵衣藻中高度偏向的密码子使用情况并不妨碍基因表达。