Method to export gene products to the growth medium of gram nega

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

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

435 91, 4351723, 4352351, 4353201, 4352523, 43525233, 536 27, 530350, 935 9, 935 27, 935 31, 935 48, 935 56, 935 58, 935 61, 935 72, 935 73, C12P 2102, C12P 1934, C12N 1500, C12N 700

Patent

active

051569590

ABSTRACT:
A process for expressing proteins in Gram(-) bacteria and providing for extracellular secretion thereof, comprising the steps: a) introducing into a Gram(-) bacterium a recombinant DNA construction comprising a promoter, a signal sequence enabling translocation and processing, and a structural gene encoding the desired protein to be expressed; b) cultivating the bacterium under conditions resulting in filamentous growth; and c) recovering the extracellularly secreted protein; a recombinant DNA construction comprising:

REFERENCES:
patent: 4338397 (1982-07-01), Gilbert et al.
patent: 4472302 (1984-09-01), Karkhanis
patent: 4624922 (1986-11-01), Horikoshi et al.
Char et al., J. Biol. Chem. vol. 260, pp. 8925-8935 (1985).
Nilsson et al., Embo vol. 4, pp. 1075-1080 (1985).
Kudo et al., J. Bacteriology, vol. 156 pp. 949-951 (1983).
Kobayashi et al., J. Bacteriology, vol. 165 pp. 728-732 (1986).
Pugsley et al., Embo, J. vol. 3 pp. 2393-2397 (1984).
Uhlin et al., Gene vol. 6 3 pp. 91-106 (1978).
Rao et al., Gene vol. 3 pp. 247-263 (1978).
Gilleland, H. E. et al., J. Bacteriol. vol. 125, pp. 267-281 (1976).
Colbert, D. et al., J. of Biol. Response Modifers vol. 3 pp. 255-259 (1984).
Abrahamsen et al., "Analysis of Signals for Secretion in the Staphylococcal Protein A Gene", The EMBO Journal, vol. 4, No. 1.
PCT Publication Number WO 84/00774 (abstract).
"Secretion of heterologous gene products to the culture medium of Escherichia coli", Nucleic Acids Research, Lars Abrahmsen, et al., vol. 14, No. 18 (1986), pp.7487-7500.
"Expression of Human Insulin-Like Growth Factor I in Bacteria: Use of Optimized Gene Fusion Vectors To Facilitate Protein Purification",Biochemistry, Tomas Moks, et al., vol. 26, No. 17 (1987), pp. 5239-5244.
"Dual expression system for generation, analysis and purification of antibodies to a repeated sequence of the Plasmodium falciparum antigen Pf155/RESA", by Stefan Stahl, et al., Department of Biochemistry and Biotechnology, Royal Institute of Technology, S-10044 Stockholm, Sweden.
"Analysis and Use of the serum Albumin Binding Domains of Streptococcal Protein G", Journal of Molecular Recognition, Per-Ake Nygren, et al., vol. 1, No. 2 (1988), pp.69-74.
"Differential stability of recombinant human insulin-like growth factor II in Escherichia coli and Staphylococcus aureus", Bjorn Hammarberg, et al., Department of Biochemistry and Biotechnology, Royal Institute of Technology, S-10044 Stockholm, Sweden.
"Analysis of the leaky phenotype of Escherichia coli induced by the expression of staphylococcal protein A", Lars Abrahmsen, et al., Department of Biochemistry and Biotechnology, Royal Institute of Technology, S-10044 Stockholm, Sweden.
"Extracellular production of cloned .alpha.-amylase by Excherichia coli", Gene, Ilari Suominen, et al., vol. 61 (1987), pp. 165-176.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Method to export gene products to the growth medium of gram nega does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Method to export gene products to the growth medium of gram nega, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Method to export gene products to the growth medium of gram nega will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-191424

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.