Abstract:
:Trichoderma reesei was transformed to hygromycin B resistance using a novel vector, which contains the E. coli hygromycin B phosphotransferase gene (hph) fused between promoter and terminator elements of the homologous Trichoderma pki1 (coding for pyruvate kinase) and cbh2 (coding for cellobiohydrolase II) genes, respectively. Transformation frequencies of over 1,800--2,500 transformants/micrograms DNA were obtained, which is a 15--20-fold increase over that with pAN7-1, which contains hph between A. nidulans expression signals. Mitotically-stable transformants contained the hph gene and the regulatory sequences of the pki1 promoter and the cbh2 terminator integrated into the genome. Evidence for preferentially ectopic integration is given.
journal_name
Curr Genetjournal_title
Current geneticsauthors
Mach RL,Schindler M,Kubicek CPdoi
10.1007/BF00351679subject
Has Abstractpub_date
1994-06-01 00:00:00pages
567-70issue
6eissn
0172-8083issn
1432-0983journal_volume
25pub_type
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