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COBRA DEVELOPS NEW GENETIC ENGINEERING TOOL FOR INSERTING GENES INTO BACTERIA
 


 

Keele, UK, 7th April 2006 - Cobra Biomanufacturing plc (AIM: CBF), the international manufacturer of biopharmaceuticals, today announces the development of a new method for inserting or deleting genes in bacteria; the Xer-cise technology. This work is described in the current edition of the prestigious international peer reviewed science publication Applied and Environmental Microbiology. Xer-cise was developed in Cobra’s research laboratories over several years and enables genes to be switched in and out of bacterial chromosomal DNA cleanly and more efficiently than current methods. Gene insertion and deletion is particularly problematic in the more novel species of bacteria of industrial interest such as Bacillus. Xer-cise is of generic utility and is simple to employ.

David Thatcher, Chief Executive of Cobra Biomanufacturing commented: “Much of Cobra’s work for our international client base is underpinned by the application state of the art genetic engineering methods to the development of their products. Xer-cise is a novel methodology invented by Cobra which will translate into accelerated drug development for our customers”.
 
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Notes To Editors:
 
About Cobra Biomanufacturing Plc
Cobra Biomanufacturing Plc is a leading international manufacturer of biopharmaceuticals to the life science industry. Founded in 1992, Cobra provides innovative manufacturing solutions to the biopharmaceutical industry covering recombinant protein products, virus, DNA and cellular therapeutics. Cobra was the first company to develop GMP (Good Manufacturing Practice) standard DNA manufacture in Europe, with specific expertise in DNA medicines.
A range of unique, patented technologies, underpins this revenue generating business.
Cobra floated on the Alternative Investment Market of the London Stock Exchange in June 2002 raising £7 million and raised a further £5.2 million in May 2003 in order to further expand capacity in Oxford UK
 
About Gene Integration
Bacteria such as Escherichia coli are very important to the biopharmaceutical industry for production of a range of therapeutics, and are genetically engineered to improve product yield and purity. This involves inserting foreign genes and deleting other genes.  Current approaches for inserting genes into or deleting genes from bacterial chromosomes rely on the use of antibiotic resistance genes to identify the cells containing the new mutations, as unmodified cells are killed in the presence of a selective antibiotic. However, these antibiotic resistance genes remain on the chromosome, resulting in antibiotic-resistant bacteria and the risk of resistance gene transfer to pathogenic organisms, thus making them unsuitable for the production of biopharmaceuticals. Also, multiple chromosomal modifications may be required, which would quickly exhaust the supply of available antibiotic resistance genes.
 
One approach to solve this problem involves flanking an antibiotic resistance gene with recombination sites: DNA sequences that are recognised by site-specific recombinase enzymes. When the new DNA is inserted into the host cell chromosome, the site-specific recombinase cuts its two target sites and joins them together to create a single site, thereby excising the intervening antibiotic resistance gene. The genes encoding the recombinase enzymes have traditionally been introduced into the cell (usually on a plasmid) and removed later.
 
Xer-cise allows genes to be inserted or deleted efficiently without permanently integrating antibiotic resistance genes. An additional advantage of Xer-cise is the ubiquitous nature of the Xer recombination system, which will allow the technology to be applied to a wide range of bacteria, including species for which only a limited range of molecular biological techniques have been developed.
 
Xer-cise is being protected through patent applications worldwide.
 
For Further Information:
Cobra Biomanufacturing Plc 
David Thatcher, Chief Executive, Tel: 44 (0) 1782 714 181 
 
Northbank Communications 
Marc Egelhofer Tel: 44 (0) 1260 296 5000
 
Buchanan Communications  
Rebecca Dietrich, Tel: 44 (0) 207 466 5000  
 
 

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