Autonomous replication sequences for yeast strains of the genus pichia
AssigneePhillips Petroleum Company
InventorJames M. Cregg
Life of this patent
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Abstract
Novel autonomous replication sequences which are capable of maintaining plasmids as extrachromosomal elements in host strains of the genus Pichia are provided. In addition, novel constructs including these DNA sequences, as well as transformed organisms therewith are provided. Processes for producing the DNA sequences and constructs of the invention, as well as method for isolating such sequences from any source, are provided.
Claims16
An isolated DNA fragment which comprises an autonomous replication sequence isolated from a strain of Pichia pastoris;
- which DNA fragment when inserted into a plasmid enables said plasmid to be maintained as an extrachromosomal element in multiple copies in a Pichia pastoris host, and which isolated DNA fragment when inserted into a plasmid causes increased frequency of transformation of a Pichia pastoris host compared to the frequency of transformation with plasmids which do not contain said isolated DNA fragment.
Escherichia coli NRRL B-15890 (LE392-pYJ30).
Escherichia coli NRRL B-15891 (LE392-pYJ32).
A process for isolating DNA sequences from Pichia pastoris;
- wherein said DNA sequences have autonomous replication sequence activity in a transformable yeast host of the species Pichia pastoris;
- said process comprising:
- (a) preparing a library of DNA fragments obtained from Pichia pastoris in a vector capable of transformation into a member of the species Pichia pastoris;
- wherein said vector comprises:
- (i) a marker gene;
- wherein said marker gene comprises a functional gene which confers a selectable phenotype upon said yeast host,
- (ii) bacterial sequences which enable transformation of bacteria with said vector, amplification of said vector in a bacterial host and selection for transformed bacterial host, but
- (iii) substantially no yeast autonomous replication sequence activity;
- (b) transforming said yeast host with said library;
- wherein said marker gene can be selected in said yeast host;
- (c) collecting transformed colonies produced in step (b) and growing them under selective conditions;
- (d) extracting total DNA from the cells which survive the selective growth conditions;
- (e) transforming competent E. coli cells with the total DNA obtained in step (d);
- (f) growing the transformed E. coli cells obtained in step (e) under selective growth conditions, wherein said selective growth conditions comprise media plus antibiotic to which said bacterial sequences provide resistance;
- (g) recovering plasmid from said transformed E. coli cells;
- (h) transforming said yeast host with the plasmid recovered in step (g);
- (i) growing up the transformed yeast host obtained in step (h) under selective growth conditions;
- (j) selecting and purifying colonies which grow well under the selective growth conditions of step (i);
- (k) transferring the purified colonies to liquid culture and growing under selective growth conditions
- (l) extracting total DNA from the cultures grown up in liquid culture;
- (m) transforming competent E. coli cells with the DNA isolated in step (1);
- (n) selecting those colonies in step (k) which gave the high transformation frequency of E. coli in step (m);
- (o) recovering plasmid from those colonies selected in step (n);
- and
- (p) removing the inserted DNA fragment contained in plasmid recovered in step (o).
Dependencies are inferred from the claim text.