Tang D K, Qiao S Y, Wu M
Dept. of Biology, Hong Kong University of Science and Technology, Kowloon.
Biochem Mol Biol Int. 1995 Aug;36(5):1025-35.
We introduced plasmid pCmVCAT containing a chloramphenicol acetyltransferase (CAT) gene, flanked by the cauliflower mosaic virus 35S promoter and nopaline synthase polyadenylation sequences, into Chlamydomonas reinhardtii by electroporation; chloramphenicol (CAM) resistance was used for selection. Several mutants with aberrant response to cadmium (Cd) toxicity were obtained by screening CAM resistant transformants. Southern blot analysis showed random integration of pCmVCAT sequence into the nuclear genome. Expression of CAT gene was confirmed by the detection of CAT gene transcript in Northern blot analysis and the detection of CAT enzyme by ELISA assay. This study demonstrated the feasibility of transforming Chlamydomonas reinhardtii with heterologous DNA by electroporation, and the expression of heterologous gene, in this alga.
我们通过电穿孔法将含有氯霉素乙酰转移酶(CAT)基因的质粒pCmVCAT导入莱茵衣藻,该基因两侧分别是花椰菜花叶病毒35S启动子和胭脂碱合酶多聚腺苷酸化序列;利用氯霉素(CAM)抗性进行筛选。通过筛选抗CAM转化体获得了几个对镉(Cd)毒性反应异常的突变体。Southern印迹分析表明pCmVCAT序列随机整合到核基因组中。通过Northern印迹分析检测CAT基因转录本以及通过ELISA测定法检测CAT酶,证实了CAT基因的表达。本研究证明了通过电穿孔法将异源DNA导入莱茵衣藻以及在这种藻类中表达异源基因的可行性。