Twin-arginine translocation in Bacillus

Chemistry: natural resins or derivatives; peptides or proteins; – Proteins – i.e. – more than 100 amino acid residues

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C435S183000, C424S192100

Reexamination Certificate

active

07884192

ABSTRACT:
Described herein are methods to enhance protein secretion in a host cell. In preferred embodiment, the host cell is a gram-positive microorganism such as aBacillus. In another preferred embodiment, the host cell is a gram-negative microorganism. Preferably the gram-negative microorganism is anEscherichia colior a member of the genusPantoea. Protein secretion may be enhanced by the overexpression of protein components of the Tat pathway. Alternatively, secretion of foreign proteins can be selectively enhanced by forming a chimeric polypeptide comprising a tat signal sequence and the protein of interest. In a preferred embodiment, the tat signal sequence is selected from phoD or LipA.

REFERENCES:
patent: 3817837 (1974-06-01), Rubenstein et al.
patent: 3850752 (1974-11-01), Schuurs et al.
patent: 3939350 (1976-02-01), Kronick et al.
patent: 3996345 (1976-12-01), Ullman et al.
patent: 4275149 (1981-06-01), Litman et al.
patent: 4277437 (1981-07-01), Maggio
patent: 4366241 (1982-12-01), Tom et al.
patent: 4816567 (1989-03-01), Cabilly et al.
patent: 5641671 (1997-06-01), Bos et al.
patent: 5804409 (1998-09-01), Bos et al.
patent: 7214773 (2007-05-01), Kolkman
patent: 0 444 759 (1991-09-01), None
patent: WO 99/51753 (1999-10-01), None
patent: WO 02/055717 (2002-07-01), None
*Altschul el et al., “Gapped BLAST and PSI-BLAST: a new generation of protein database programs,” Nucl. Acids Res., vol. 25, pp. 3389-3402, 1997.
*Antelmann el al., “Expression of a Stress- and Starvation-induced dps/pexB—Homologous Gene Is Controlled by the Alternative Sigma Factor oBinBacillus bacillus,” J. of Bacteriology, vol. 179, pp. 7251-7256, 1997.
*Antelmann el al., “Phosphate Starvation-Inducible Proteins ofBacillus bacillus: Proteomics and Transcriptional Analysis,” J. of Bacteriology, vol. 182, pp. 4478-4490, 2000.
*Bakhiet et al., “Studies on Transfection and Transformation of Protoplasts ofBacillus larvae, Bacillus subtilis,andBacillus popilliae,” Applied and Environmental Microbiology, vol. 49, No. 3, pp. 577-581, Mar. 1985.
*Benton et al., “Steering λgt Recombinant Clones by Hybridization to Single Plaques in situ,”Science, vol. 196, No. 4286, pp. 180-182, Apr. 8, 1977.
*Berger and Kimmel, Guide to Molecular Cloning Techniques, Methods in Enzymology, vol. 152, Academic Press, San Diego, CA (1987).
*Berks B., “A common export pathway for proteins binding complex redox cofactors,” Mol Microbiol. vol. 22, pp. 393-404, 1996.
*Berks et al., “The Tat protein export pathway,” Mol Microbiol. vol. 35, pp. 260-274, 2000.
*Bernhardt et al., “Specific and general stress proteins inBacillus subtilis—a two-dimensional protein electrophoresis study,” Microbiol. vol. 143, pp. 999-1017, 1997.
*Database EMBL, Blattner F.R. et al., << Hypothetical 11.3 KD Protein in UDP-RFAH Intergenic Region (TATA Protein), Database accession No. 065938, XP002133194.
*Blum et al., “Improved silver staining of plant proteins, RNA and DNA in polyacrylamide gels,” Electrophoresis, vol. 8, pp. 93-99, 1987.
*Bogsch et al., “Pathway specificity for a ΔpH-dependent precursor thylakoid lumen protein is governed by a ‘Sec-avoidance’ motif in the transfer peptide and a ‘Sec-incompatible’ mature protein,” EMBO, vol. 16, pp. 3851-3859, 1997.
*Bogsch et al., “An Essential Component of a Novel Bacterial Protein Export System with Homologues in Plastids and Mitochondria,” J. Biol. Chem., vol. 273, pp. 18003-18006, 1998.
*Bolhuis et al., “Evaluation of Bottlenecks in the Late Stages of Protein Secretion inBacillus subtilis,” App. Environ. Microbiol. vol. 65, pp. 2934-2941, 1999.
*Bolhuis et al., “Different Mechanisms for Thermal Inactivation ofBacillus subtilisSignal Mutants,” J. Biolog. Chem., vol. 274, pp. 15865-15868, 1999.
*Bolhuis et al., “Bacillus subtilis, can modulate its capacity and specificity for protein secretion through temporally controlled expression of thesipSgene for signal peptidase I” Mol. Microbiol. vol. 22, pp. 605-618, 1996.
*Brink et al., “Targeting of thylakoid proteins by the ΔpH-driven twin-arginine translocation pathway requires a specific signal in the hydrophobic domain in conjunction with the twin-arginine motif,” FEBS Letters, vol. 434, pp. 425-430, 1998.
*Bron et al., “Construction and Characterization of a Transformable Eightfold Auxotrophic Strain and two Ultraviolet-Sensitive Derivatives,” Mutation Research, vol. 15, pp. 1-10, 1972.
*Chaddock et al., “A new type of signal peptide: central role of a twin-arginine motif in transfer signals for the ΔpH-dependent thylakoid protein translocase,”EMBO, vol. 14, pp. 2715-2722, 1995.
*Chanal et al., “MicroCorrespondence,” Molec. Microbiol. vol. 30, pp. 673-678, 1998.
*Chang et al., “High Frequency Transformation ofBacillus subtilisProtoplasts by Plasmid DNA,”Molec. Gen. Genet.vol. 168, pp. 111-115, 1979.
*Coombs, J.,Dictionary of Biotechnology, Stockton Press, New York, N.Y., 1994.
*Contente et al., “Marker Rescue Transformation by Linear Plasmid DNA inBacillus subtilis,” Plasmid, vol. 2, pp. 555-571, 1979.
*Cristobal et al., Competition between Sec- and TAT-dependent protein translocation inEscherichia coli, EMBO, vol. 18 pp. 2982-2990, 1999.
*Cserzo et al., “Prediction of transmembrane α-helices in prokaryotic membrane proteins: the dense alignment surface method,” Protein Engin. vol. 10 pp. 673-676, 1997.
*Dalbey et al., “Protein translocation into and across the bacterial plasma membrane and the plant thylakoid membrane,” TIBS, vol. 24, pp. 17-21, 1999.
*Database EMBL, Daniels D. L. et al., << Deoxyribonuclease tatD, >> Database accession No. P27859, XP002227139.
*Dieffenbach et al.,PCR Primer, a Laboratory Manual, Cold Springs Harbor Press, Plainview, N.Y., 1995.
*Donovan et al., “Genes Encoding Spore Coat Polypeptides fromBacillus subtilis,” J. Mol. Biol., vol. 196, pp. 1-10, 1987.
*Eder et al., “Bacillus subtilissecreted phosphodi esterase/alkaline phosphatase in the product of a Pho regulon gene, phoD,” Microbiology, vol. 142, pp. 2041-2047, 1996.
*Eymann et al., “Phosphate-starvation-inducible proteins inBacillus subtilis: a two-dimensional gel electrophoresis study,” Microbiology, vol. 142, pp. 3163-3170, 1996.
*Fischer et al., “Introduction of plasmid pC194 intoBacillus thuringiensisby Protoplast transformation and plasmid transfer,”Archives of Microbiology, vol. 139, pp. 213-217, 1984.
*Glover, D. M. (ed), DNA Cloning: A Practical Approach, MRL Press, Ltd., Oxford, U. K. vol. I, II.
*Grunstein et al., “Colony hybridization: A method for the isolation of cloned DNAs that contain a specific gene,”Proc. Nat. Acad. Sci.USA, vol. 72, No. 10, pp. 3961-3965, Oct. 1975.
*Haima, Peter et al., “Novel plasmid marker rescue transformation system for molecular cloning inBacillus subtilisenabling direct selection of recombinants,”Mol. Gen. Genet.vol. 223, pp. 185-191, 1990.
*Hale & Marham, The Harper Collins Dictionary of Biology, Harper Perennial, NY (1991).
*Hampton, R. et al.,Serological Methods, a Laboratory Manual, APS Press, St. Paul, MN. 1990.
*Harwood et al.,Molecular Biological Methods for Bacillus, John Wiley & Sons, 1990.
*Hirose et al., “Proteome analysis ofBacillus subtilisextracellular proteins: a two-dimensional protein electrophoretic study,” Microbiology, vol. 146, pp. 65-75, 2000.
*Holubova et al., “Transfer of Liposome-Encapsulated Plasmid DNA toBacillus subtilisProtoplasts and Calcium-TreatedEscherichia coliCells,” Folia Microbiol. vol. 30, pp. 97-100, 1985.
*Hulett et al., “Evidence for Two Structural Genes for Alkaline Phosphatase inBacillus subtilis,” J. Bacteriol. vol. 172, pp. 735-740, 1990.
*Hynds et al.,

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

Twin-arginine translocation in Bacillus does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Twin-arginine translocation in Bacillus, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Twin-arginine translocation in Bacillus will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2627564

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