Expression vector for human TNF

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

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4351723, 4353201, 43525233, 935 11, 935 29, 935 31, 935 42, 935 56, 935 65, 536 27, C07H 1512, C12P 202, B61K 3702, C12N 120

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050595300

ABSTRACT:
The present invention provides a vector plasmid capable of efficient tumor necrosis factor (TNF) production, a process capable of efficient TNF production in a host transformed with said plasmid and a composition containing the TNF produced by said process.
The novel plasmid of the present invention is characterized by having inserted therein a DNA fragment that has a phage-derived promoter region upstream of a structural gene for TNF and in which a DNA fragment containing an E. coli gene-derived transcription termination coding base sequence (terminator) is joined immediately downstream of a base sequence coding for the termination of translation of said structural gene.

REFERENCES:
patent: 4871663 (1989-10-01), Ohshima et al.
Platt, T. Cell vol. 24, pp. D-23, Apr. 1981, "Termination of Transcription and 180 Regulation of the Tryptophehopeonin E Coli".
Lacatena, et al., Cell vol. 37, pp. 1004-1014, Jul. 19 & 7, "Control of Initiation of pMB1 Replication: Purified Rop Protein and RNA I Affect Primer Formation in Vitro".
Nature, vol. 312, Dec. 20/27, 1984-D. Pennica et al., "Human Tumor Necrosis Factor: Precursor Structor, Expression and Homology to Lymphotoxin", pp. 724, 725.
Science, vol. 228, No. 4696, Apr. 12, 1985-A. M. Wang et al., "Molecular Cloning of the Complementary DNA For Human Tumor Necrosis Factor", pp. 149-154.

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