摘要
为了研究红曲霉聚酮体途径，考察和比较了4种不同的转化方法以建立有效的红曲霉遗传转化系统。以潮霉素作为抗性筛选标记，pBC-Hygro作为转化载体，用基于原生质体的传统转化和电击转化、基于萌发孢子的电击转化以及REMI技术转化红曲霉。发现基于萌发孢子的电击转化由于转化率极低而不适于红曲霉转化。基于原生质体的传统转化和电击转化尽管每微克DNA分别能获得135个转化子和125个转化子，但因转化子稳定性差也适合红曲霉转化的转化。应用REMI技术，转化率提高约20倍，每微克DNA 2500个转化子，70％～75％的转化子的稳定，非常适合于红曲霉的转化。
In order to facilitate the producer of polyketide pathway, four different transformation methods were tested and compared in an attempt to develop the genetic transformation system of Monascus sp.. Using vector pBC-Hygro, the fungus was transformed to be hygromycin B-resistant, by conventional transformation as well as electroporation based on protoplast, electroporation based on germinated conidia, and restriction enzyme-mediated integration （REMI）. Electroporation based on germinated conidia was found to be inappropriate for transforming Monascus sp. due to a low transformation frequency. The conventional transformation and electroporation technique based on protoplasts were thought not to be fit for transforming Monascus sp., due to a low stability of transformants though they yielded up to 135 transformants and 125 transformants per microgrammol/Lol/Le DNA, respectively, Transformant number was increased by 20-fold by REMI （2 500 transformants per microgrammol/Lol/Le DNA） and 70% -75% of them were stable. REMI technique would be very beneficial to the establishment of the genetic transformation system of Monascus sp..
出处
《遗传》
CAS
CSCD
北大核心
2006年第4期479-485,共7页
Hereditas（Beijing)
关键词
红曲霉
遗传转化
电击转化
REMI
Monascus sp.
genetic transformation
electroporation
REMI
