Method for producing and cloning SacII restriction endonuclease and methylase
AssigneeNew England Biolabs, Inc.
InventorsEllen P. Guthrie, Marta M. Meda
Life of this patent
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Abstract
The present invention is directed to a method for cloning and producing the SacII restriction endonuclease by 1) introducing the restriction endonuclease gene from Streptomyces achromogenes into a host whereby the restriction gene is expressed; 2) fermenting the host which contains the plasmid encoding and expressing the SacII restriction endonuclease activity, and 3) purifying the SacII restriction endonuclease from the fermented host which contains the plasmid encoding and expressing the SacII restriction endonuclease activity.
Claims12
A method for cloning DNA for a SacII restriction endonuclease comprising;
- a) purifying DNA from Streptomyces achromogenes ATCC No. 12767;
- b) digesting the purified DNA with EcoRV to form DNA fragments;
- c) ligating the DNA fragments into the cloning vector pJRD184;
- d) transforming a host cell with the cloning vector of step c) to form a cell library;
- e) purifying recombinant vectors from the cell library to form a plasmid library;
- f) contacting the plasmid library of step e) with SacII to form a digestion pool, transforming the digestion pool into a host cell, and screening for the presence of one or more cloning vectors containing DNA coding for a SacII methylase;
- g) subcloning the DNA obtained in step f) which contains DNA coding for SacII methylase into a Streptomyces compatible cloning vector;
- h) transforming Streptomyces lividans host cell with the cloning vector of step g);
- and
- i) screening the transformants of step h) for the presence of DNA coding for a SacII restriction endonuclease by identifying transformants which produce the SacII restriction endonuclease.
A method of producing SacII restriction endonuclease comprising;
- a) purifying DNA from Streptomyces achromogenes ATCC No. 12767;
- b) partially digesting the purified DNA with EcoRV to form DNA fragments;
- c) ligating the DNA fragments into the cloning vector pCU19;
- d) transforming a host cell with the cloning vector of step c) to form a cell library;
- e) purifying recombinant vectors from the cell library to form a plasmid library;
- f) contacting the plasmid library of step e) with SacII to form a digestion pool, transforming the digestion pool into a host cell, and screening for the presence of one or more cloning vectors containing DNA coding for a SacII methylase;
- g) subcloning the DNA obtained in step f) which contains DNA coding for SacII methylase into a Streptomyces compatible cloning vector;
- h) transforming Streptomyces lividans host cell with the cloning vector of step g);
- i) screening the transformants of step h) for the presence of DNA coding for a SacII restriction endonuclease by identifying transformants which produce the SacII restriction endonuclease;
- and
- j) culturing the transformants of step i) under conditions suitable for expression of the SacII restriction endonuclease.
Isolated DNA consisting essentially of DNA coding for the Sac II restriction endonuclease, wherein the isolated DNA is endogenous to Streptomyces achromogenes ATCC Accession No. 12767.
A recombinant DNA vector comprising a vector into which a DNA segment coding for the Sac II endonuclease produced by Streptomyces achromogenes ATCC Accession No. 12767 has been inserted.
Dependencies are inferred from the claim text.