Promoters and gene expression method by using the promoters

Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Recombinant dna technique included in method of making a...

Reexamination Certificate

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C435S252310, C435S252330, C435S320100, C536S023100, C536S024100

Reexamination Certificate

active

10258482

ABSTRACT:
To provide a promoter, a recombinant DNA, a gene expression vector, an expression vector, and a transformant, which are capable of expressing a gene without inducing gene expression with an inducer; and a method for producing a protein and a kit therefor, which can be operated easily and performed inexpensively by convenient and inexpensive steps. An isolated DNA having the nucleotide sequence of SEQ ID NO: 1 or 2 of Sequence Listing or a fragment thereof, wherein the isolated DNA exhibits a constitutive promoter activity inEscherichia colior a bacterium belonging to the genusBacillus; an isolated DNA having a nucleotide sequence of a nucleic acid capable of hybridizing to the above DNA, wherein the isolated DNA exhibits a constitutive promoter activity inEscherichia colior a bacterium belonging to the genusBacillus; a recombinant DNA comprising the above DNA and a foreign gene, wherein the foreign gene is operably located; a gene expression vector, at least comprising the above DNA; an expression vector comprising the recombinant DNA; a transformant having the above recombinant DNA, or the above expression vector; a method for producing a protein, characterized by culturing the above transformant, and collecting a protein from the resulting culture; and a kit for producing a protein, at least comprising the above DNA, or the above gene expression vector.

REFERENCES:
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patent: 99039948 (1999-06-01), None
Ian G. Fotheringham et al.; Journal of Bacteriology, vol. 180, No. 16, Aug. 1998, pp. 4319-4323.
Kor. J. Microbiol. Biotechnol., vol. 27, pp. 184-190 (1999).
Biochimica et Biophysica ACta, vol. 1350, No. 1, pp. 38-40 (1997).

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