Ikushima Shigehito, Minato Toshiko, Kondo Keiji
Central Laboratories for Frontier Technology, KIRIN Holdings Co., Ltd.
Biosci Biotechnol Biochem. 2009 Jan;73(1):152-9. doi: 10.1271/bbb.80568. Epub 2009 Jan 7.
In order to develop practical recombinant DNA techniques in the industrially important yeast Candida utilis, at least six plasmids harboring autonomously replicating sequences (ARSs) were isolated from a C. utilis genomic library. Two ARSs were subjected to detailed analysis. Sequences of 1.9 and 1.8 kb were found to be necessary to exert ARS activity in a plasmid as assessed by transformation efficiency and mitotic stability. Both fragments were found to be rich in AT content (69.5% and 70.8% respectively), and to contain an 11-bp ARS consensus sequences (10 and 13 motifs with one base difference respectively). Using the ARS-containing plasmid as a promoter-cloning vector, several DNA fragments having promoter activities were cloned and characterized. Co-transformation of C. utilis with an integrating DNA fragment and a replicating plasmid yielded plasmid-free transformants harboring the fragment integrated into the C. utilis genome.
为了在具有重要工业价值的产朊假丝酵母中开发实用的重组DNA技术,从产朊假丝酵母基因组文库中分离出至少六个含有自主复制序列(ARS)的质粒。对其中两个ARS进行了详细分析。通过转化效率和有丝分裂稳定性评估,发现1.9 kb和1.8 kb的序列对于在质粒中发挥ARS活性是必需的。发现这两个片段富含AT含量(分别为69.5%和70.8%),并包含一个11 bp的ARS共有序列(分别有10个和13个基序,相差一个碱基)。使用含ARS的质粒作为启动子克隆载体,克隆并表征了几个具有启动子活性的DNA片段。将整合DNA片段与复制质粒共转化产朊假丝酵母,产生了不含质粒的转化体,其中该片段整合到产朊假丝酵母基因组中。