Abstract: A method of increasing xanthan gum production, comprising culturing a Xanthomonas campestris strain having a xanthan-increasing modification in a culture medium, wherein the modification is selected from the group consisting of (1) a mutation causing rifampicin-resistance; (2) a mutation causing bacitracin-resistance; or (3) exogenous genetic information controlling the synthesis of xanthan; and separating xanthan from the culture medium, is provided along with specific DNA sequences and Xanthomonas campestris strains showing increased xanthan gum production.
Type:
Grant
Filed:
February 13, 1992
Date of Patent:
August 23, 1994
Assignees:
Shin-Etsu Chemical Co., Ltd., Shin-Etsu Bio, Inc.
Abstract: In a process for the production of a soluble native protein, such as immunoglobulin or methionine-prochymosin, in which an insoluble form of the protein is produced by a host organism transformed with a vector including a gene coding for the protein, the insoluble form of the protein is reversibly denatured in an alkaline aqueous solution at a pH selected to promote dissociation of a group or groups of the protein involved in maintaining the conformation of the protein, and the protein is subsequently allowed to renature by reducing the pH of the solution below a pH effective to denature the protein to produce the soluble native form of the protein. The pH of the alkaline aqueous is suitably in the range 9.0 to 11.5.
Type:
Grant
Filed:
August 5, 1993
Date of Patent:
August 23, 1994
Assignee:
Celltech, Limited
Inventors:
Peter A. Lowe, Fiona A. O. Marston, Sarojani Angal, Joyce A. Schoemaker
Abstract: Disclosed is a recombinant vertebrate F such as vaccinia virus which comprises in its genome (i) spheroidin promoter of entomopoxvirus such as Choristoneura biennis and (ii) at least one structural gene coding for at least one protein foreign to entomopoxvirus and to the vertebrate poxvirus and is capable of expressing the foreign protein gene in a vertebrate tissue culture cell or in a vertebrate animal susceptible to the vaccinia virus. The recombinant virus is capable of expressing the foreign gene at a significantly higher rate due to the presence of the entomopoxvirus spheroidin promoter than the same virus without the entomopoxvirus promoter. The protein may be antigenic or otherwise pharmaceutically useful. Also disclosed vaccine and a process for producing the protein using the recombinant virus.
Type:
Grant
Filed:
January 8, 1991
Date of Patent:
August 16, 1994
Assignee:
Her Majesty the Queen in right of Canada, as represented by National Research Council Canada and Forestry Canada
Abstract: A random peptide library constructed by transforming host cells with a collection of recombinant vectors that encode a fusion protein comprised of a DNA binding protein and a random peptide and also contain a binding site for the DNA binding protein can be used to screen for novel ligands. The screening method results in the formation of a complex comprising the fusion protein bound to a receptor through the random peptide ligand and to the recombinant DNA vector through the DNA binding protein.
Abstract: Novel methods and microorganisms are provided, where novel genetic mammalian cell invasive capability is imparted to a microorganism by the introduction of an exogenous inv gene. The resulting organisms are then capable of binding to mammalian cells and are transferred to the cytoplasm. Other novel genetic capabilities may be imparted to the unicellular microorganism, which may serve as a vaccine for one or more pathogens or may introduce genetic capabilities or foreign molecules into a mammalian host cell. The sequences may be used for an in vitro screen for pathogenicity.
Type:
Grant
Filed:
May 22, 1992
Date of Patent:
August 16, 1994
Assignee:
The Board of Trustees of Leland Stanford Jr. University
Inventors:
Ralph R. Isberg, Virginia Miller, Stanley Falkow
Abstract: A process for producing live, non-pathogenic, vaccines for the pathogens RNA turmor virus utilizes gene-altering technology to produce an altered genome which codes for the antigenic determinants of a pathogen, but has no genes coding for pathogenicity. The vaccine is the phenotypic expression of the altered genome. Specifically, an avian RNA tumor virus env gene is cloned into the non-pathogenic RNA virus RAV-O and the resulting recombinant product is replicated in host cells to provide a recombinant vaccine for the pathogen avian RNA tumor virus.
Abstract: A method of increasing xanthan gum production, comprising culturing a Xanthomonas campestris strain having a xanthan-increasing modification in a culture medium, wherein the modification is selected from the group consisting of (1) a mutation causing rifampicinresistance; (2) a mutation causing bacitracin-resistance; or (3) exogenous genetic information controlling the synthesis of xanthan; and separating xanthan from the culture medium, is provided along with specific DNA sequences and Xanthomonas campestris strains showing increased xanthan gum production.
Type:
Grant
Filed:
January 24, 1992
Date of Patent:
August 16, 1994
Assignees:
Shin-Etsu Chemical Co., Ltd., Shin-Etsu Bio, Inc.
Abstract: The kil-kor system from the plasmid pIJ101 can be utilized for regulated gene expression in Streptomycetes. For this, the KorA protein is either inactivated or eliminated to "switch on" a particular gene.
Type:
Grant
Filed:
July 23, 1993
Date of Patent:
August 9, 1994
Assignee:
Hoechst Aktiengesellschaft
Inventors:
Wolfgang Wohlleben, Gunter Muth, Alfred Puhler, Gunther J. Rieb
Abstract: Transformed yeasts comprising DNA which include at least one copy of a fragment coding for a 1,4-.beta.-N-acetylmuramidase which is expressed in the yeasts as the corresponding active protein, and a process for preparing lysozyme by growing said transformed yeasts.
Abstract: An expression enhancer has a DNA sequence which is capable of forming a t-RNA clover-leaf structure after transcription and hybridizes in that region of the DNA which, after transcription, forms the anticodon loop in the clover-leaf structure with an oligonucleotide with the sequence 5'-GACTTAGAAGGTCGTT-3' or its complementary sequence (5'-AACGACCTTCTAAGTC-3'). It can be used to increase the yield in the expression of a recombinant gene by transformation of suitable host cells with an expression vector containing the recombinant gene, whereby it is likewise introduced into the host cells in a form capable of expression and expressed.
Type:
Grant
Filed:
January 22, 1993
Date of Patent:
August 9, 1994
Assignee:
Boehringer Mannheim GmbH
Inventors:
Ulrich Brinkmann, Ralf Mattes, Peter Buckel
Abstract: Fowlpox virus (FPV) or other avipox virus promoter DNA for use in expressing a foreign gene inserted in a FPV vector by homologous recombination, which comprises the promoter of the following 4a gene, said 4a gene encoding a protein of very roughly about 890 amino acids in a sequence beginningMet Met Leu Ile Lys Asn Ile Val Thr LeuAsp Gln Leu Glu Ser Ser Asp Tyr Leu Tyr.
Type:
Grant
Filed:
January 17, 1992
Date of Patent:
July 26, 1994
Assignee:
British Technology Group Limited
Inventors:
Matthew M. Binns, Michael E. G. Boursnell, Joan I. A. Campbell
Abstract: The production of recombinant chymosin is disclosed in which an insoluble form of chymosin precursor is produced by a bacterial host cell transformed by a vector including a coding sequence for said precursor. Solubilization of said insoluble form of chymosin precursor is accomplished using urea at a concentration of at least 7M or guanidine hydrochloride at a concentration of at least 6M prior to cleaving said precursor to form chymosin. Said solubilization preferably additionally involves the denaturation of said precursor in an alkaline aqueous solution, e.g., at a pH between a 9 and 11.
Type:
Grant
Filed:
March 29, 1991
Date of Patent:
July 26, 1994
Assignee:
Celltech Limited
Inventors:
Norman H. Carey, Michael T. Doel, Timothy J. R. Harris, Peter A. Lowe
Abstract: A process for the production of HSA in Pichia pastoris cells comprising cultivating Pichia pastoris cells capable of expressing HSA at a pH of about 5.7 to about 6.4 contemporaneously with the expression of HSA.
Type:
Grant
Filed:
April 25, 1991
Date of Patent:
July 19, 1994
Assignee:
Research Corporation Technologies, Inc.
Inventors:
William D. Prevatt, Kotikanyadan Sreekrishna
Abstract: An improved method for detecting antibodies is disclosed. The method involves the steps of a) mixing the specimen with a diluent comprising superoxide dismutase, and b) contacting the diluted specimen with at least one recombinant antigen expressed as a fusion protein with superoxide dismutase.
Type:
Grant
Filed:
May 10, 1993
Date of Patent:
July 19, 1994
Assignee:
Abbott Laboratories
Inventors:
Adrienne L. Gilbert, James L. Stewart, Sarah L. Kidd, George J. Dawson
Abstract: Methods for isolating thymidine kinase-encoding DNA of a herpes virus are described. These methods utilize degenerate primers based on regions of relatively conserved amino acid sequence in herpes virus thymidine kinase proteins to initiate a polymerase chain reaction which yields large amounts of the thymidine kinase-encoding DNA. The methods are illustrated in the isolation of the thymidine kinase gene of feline herpes virus, which can be used to construct recombinant thymidine kinase-negative feline herpes viruses for purposes of constructing live vaccines and expression vectors. In addition, the regulatory elements of the feline herpes virus thymidine kinase gene are useful in the construction of recombinant DNA vectors.
Type:
Grant
Filed:
January 21, 1993
Date of Patent:
June 28, 1994
Assignee:
The Upjohn Company
Inventors:
Jack H. Nunberg, Leonard E. Post, Teresa Compton, Erik A. Petrovskis
Abstract: Proteins, and corresponding DNA and RNA sequences, useful for the regulation of expression of .kappa.B-containing genes are disclosed. These proteins are useful to either stimulate or inhibit the expression of .kappa.B-containing genes. Proteins stimulating the expression of .kappa.B-containing genes have an amino acid sequence at least 80% identical to the amino acid sequence of from position 1 to position 374 of p100 [SEQ ID NO: 2]. Proteins having an inhibitory effect on the expression of .kappa.B-containing genes have sequences either at least 80% identical to the amino acid sequence of from position 407 to the carboxyl end of p100 [SEQ ID NO: 2] or having an amino acid sequence at least 80% identical to the amino sequence of either from position 1 to 100 sor from position 101 to position 374 of p100 [SEQ ID NO: 2].
Type:
Grant
Filed:
August 21, 1991
Date of Patent:
June 28, 1994
Assignee:
The Regents of the University of Michigan
Inventors:
Gary J. Nabel, Roland M. Schmid, Neil D. Perkins
Abstract: A method of introducing expressible heterologous DNA into Prevotella ruminicola is provided. The method involves conjugal transfer of a shuttle vector comprising the heterologous DNA operatively linked to a promoter functional in P. ruminicola. The invention also provides shuttle vectors for use in the method and P. ruminicola produced by the method. The invention further provides a tetracycline resistance gene of the TetQ class, or fragments thereof that confer tetracycline resistance, and a protein of the TetQ class that provides resistance to tetracycline by protecting ribosomes from tetracycline, or active fragments thereof. Finally, the invention provides a promoter functional in P. ruminicola and an engineered P. ruminicola comprising expressible foreign DNA.
Type:
Grant
Filed:
June 5, 1991
Date of Patent:
June 21, 1994
Assignees:
The Board of Trustees of the University of Illinois, Urbana-Champaign, Illinois, Biotechnology Research and Development Corporation
Inventors:
Abigail A. Salyers, Nadja B. Shoemaker, Mikeljon P. Nikolich
Abstract: Escherichia coil carrying a hybrid plasmid having been constructed by inserting a desired foreign gene into an expression vector so as to permitting expression of said desired foreign gene therein was cultured at a temperature 40.degree. C. or over so that the expression of said desired foreign gene was suppressed. This E. coil (i.e., transformant) was cultured at 40.degree. C. or over in a first process to suppress the expression of the foreign gene and to support sufficient cell growth and thereafter below 40.degree. C. in a second process to release the suppression of the expression so as to permit effective production of the foreign gene product, which resulted in high concentration of the foreign gene product in the final culture.
Abstract: Methods of determining collagen degradation in vivo, by quantitating the concentration of a peptide in a body fluid, the peptide having the following structure: ##STR1## is hydroxylysyl pyridinoline or lysyl pyridinoline, and J is pyroglutamic acid or glutamine and (Leu) are optional leucines, are disclosed.Compositions useful in quantitating collagen peptides to determine the rate of bone resorption are prepared by treating bone with a protease, such as collagenase, and purifying the compositions so as to enrich them with peptides capable of binding to the monoclonal antibody MAb-1H11.
Abstract: The present invention provides novel assays for determining the ability of a test compound to inhibit intercellular adhesion mediated by a selectin receptor, such as the LHR. The assays involve contacting the test compound with the receptor and an isolated receptor-binding agent. The receptor-binding agent is a sulfated polysaccharide, a sulfated glycolipid, or a compound comprising the extracellular region of an endothelial cell surface glycoprotein. Also provided are compositions comprising a compound comprising the extracellular region of an endothelial cell surface protein, which is specifically recognized by lymphocyte homing receptors.
Type:
Grant
Filed:
May 6, 1991
Date of Patent:
June 7, 1994
Assignee:
The Regents of the University of California
Inventors:
Steven Rosen, Mark Singer, Yasuyuki Imai, Ted Yednock