EXGENOMES

Exgenome Molecular Enzymes

 Coordinatore PROKAZYME EHF 

 Organization address address: VINLANDSLEIO 14
city: REYKJAVIK
postcode: 113

contact info
Titolo: Dr.
Nome: Jakob
Cognome: Kristjansson
Email: send email
Telefono: +354 664 7908

 Nazionalità Coordinatore Iceland [IS]
 Totale costo 1˙247˙115 €
 EC contributo 916˙600 €
 Programma FP7-SME
Specific Programme "Capacities": Research for the benefit of SMEs
 Code Call FP7-SME-2011
 Funding Scheme BSG-SME
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-12-01   -   2013-11-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    PROKAZYME EHF

 Organization address address: VINLANDSLEIO 14
city: REYKJAVIK
postcode: 113

contact info
Titolo: Dr.
Nome: Jakob
Cognome: Kristjansson
Email: send email
Telefono: +354 664 7908

IS (REYKJAVIK) coordinator 332˙749.00
2    A&A BIOTECHNOLOGY SC

 Organization address address: AL ZWYCIESTWA 96/98
city: GDYNIA
postcode: 81451

contact info
Titolo: Dr.
Nome: Slawomir
Cognome: Dabrowski
Email: send email
Telefono: +48 58 7351182
Fax: +48 58 6228578

PL (GDYNIA) participant 285˙840.00
3    TOUCHLIGHT GENETICS LIMITED

 Organization address address: QUEEN ANNE STREET 40
city: LONDON
postcode: W1G 9EL

contact info
Titolo: Dr.
Nome: Neil
Cognome: Porter
Email: send email
Telefono: +44 1372 822205

UK (LONDON) participant 154˙177.00
4    EXIQON A/S

 Organization address address: Bygstubben 9
city: VEDBAEK
postcode: 2950

contact info
Titolo: Dr.
Nome: Peter
Cognome: Mouritzen
Email: send email
Telefono: +45 45 66 08 88

DK (VEDBAEK) participant 143˙834.00
5    IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE

 Organization address address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
city: LONDON
postcode: SW7 2AZ

contact info
Titolo: Ms.
Nome: Tatjana
Cognome: Palalic
Email: send email
Telefono: +44 020 7594 3866

UK (LONDON) participant 0.00
6    INTERNATIONAL INSTITUTE OF MOLECULAR AND CELL BIOLOGY

 Organization address address: ks. Trojdena 4
city: Warsaw
postcode: 02-109

contact info
Titolo: Prof.
Nome: Janusz
Cognome: Bujnicki
Email: send email
Telefono: +48 22 5970750
Fax: +48 22 5970715

PL (Warsaw) participant 0.00
7    MATIS OHF

 Organization address address: VINLANDSLEID 12
city: REYKJAVIK
postcode: 112

contact info
Titolo: Dr.
Nome: Gudmunur
Cognome: Hreggvidsson
Email: send email
Telefono: +354 422 5047

IS (REYKJAVIK) participant 0.00
8    UNIWERSYTET GDANSKI

 Organization address address: ul. Bazynskiego 1a
city: GDANSK
postcode: 80952

contact info
Titolo: Prof.
Nome: Tadeusz
Cognome: Kaczorowski
Email: send email
Telefono: +48 58 305 6242
Fax: +48 58 5236420

PL (GDANSK) participant 0.00

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

source    self    nucleases    expressed    reverse    replicating    ligases    purified    selected    thermostable    plasmids    phages    genetic    pharmaceutical    enzymes    sme    nucleic    polymerases    phage    commercial    lysozymes    ssb    transcriptases    polymerase    candidate    technologies    exgenomes    evaluation    dna    transposons    protelomerases    characterised    mobile    lna    lysozyme    cloned    recombinase    industry    polynucleotide    acids    synthesis    biotechnology    thermus    vaccine    kinases    thermophilic    addition    diagnostics    bacteria   

 Obiettivo del progetto (Objective)

'The main objective of the EXGENOMES project is to develop new and improved thermostable enzymes for use, as reagents, in large-scale DNA synthesis and/or that can act on unnatural components such as in LNA (Locked Nucleic Acids). The target source for the new enzymes is a range of self-replicating mobile genetic elements (phages, plasmids and transposons) from thermophilic bacteria. Increased understanding of self-replication in many mobile genetic elements, such as phi29, has now made the commercial development of new self-priming & strand-displacing polymerases and other enzymes, much more plausible. A number of candidate enzymes, such as a new transposon-coded Thermus DNA polymerase are at hand for this project in the thermophilic bacteria & phage genome bank at Matis.

Nucleic acids based technologies now underpin a large and fast-growing industry, including research, diagnostics and pharmaceutical production. Thermophilic enzymes have played a key role in this development, as polymerases (DNA and RNA), ligases, nucleases, reverse transcriptases, polynucleotide kinases, lysozymes and more, are of great importance in the research industry today. The partner SME´s are all active players in this area from bioprospecting (Prokazyme), laboratory distribution (A&A Biotechnologies), LNA manufacture & diagnostics (Exiqon) to DNA vaccine production (Touchlight Genetics).

Together with the highly competent RTD partners the consortium is well positioned to implement the project according to its goals. The successful development of new thermostable polymerases and other enzymes with the desired properties would have a substantial impact on strengthening the current market status of the SME partners, resulting in growth in income and employment.'

Introduzione (Teaser)

Thermostable enzymes, such as polymerases, ligases, nucleases, reverse transcriptases, polynucleotide kinases and restriction enzymes play an important role in biotechnology. Increased use of DNA-based technologies dictates the need for discovery and production of new thermostable enzymes.

Descrizione progetto (Article)

Thermophilic microorganisms are a subject of intense research. Thermostable enzymes found in thermophilic bacteria are produced recombinantly and used both in industry and biotechnology. For example, the thermostable enzyme Taq-polymerase is used in polymerase chain reaction, a very sensitive and widespread tool for genetic analysis.

The search for new thermostable enzymes continues. The project 'Exgenome Molecular Enzymes' (EXGENOMES) intended to develop new and improved enzymes for use in large-scale DNA synthesis. The target source for the new enzymes were self-replicating mobile genetic elements (phages, plasmids and transposons) from thermophilic bacteria.

In addition to using existing genetic databases for thermophilic bacteria and phages, novel genetic material was obtained from hot springs in Iceland and sequenced. The candidate genes were selected, cloned and expressed. Produced enzymes were purified, characterised and tested.

A total of 39 new enzymes were selected for cloning and expression, out of which 23 enzymes were produced and purified for activity evaluation. Eight types of thermostable enzymes were represented, such as DNA polymerases, protelomerases, lysozymes, helicase, RNAse H, Rec A, primase and single-stranded DNA binding protein (SSB). After activity evaluation, 14 enzymes were further purified and characterised, and finally 6 enzymes were developed into commercial products. These are: LysT lysozyme from Thermus phage Pro2631; Lys2119 lysozyme from Thermus phage Ph2119; RecA recombinase from Thermus phage T72; RadA recombinase from Pyrococcus woesei; Pol72 DNA polymerase from Thermus islandicus; and SSB M2 from metagenome.

In addition, two new protelomerases, TelA and TelK, were cloned, expressed, purified and used for experiments in making new DNA vaccine constructs. New enzymes were described in six scientific publications, and two patents were filed.

Development of new thermostable enzymes for commercial applications promises benefits for the smaller enterprises involved in the project. It also boosts EU competitiveness in the biotechnology sector for applications in health care and pharmaceutical industries.

Altri progetti dello stesso programma (FP7-SME)

DASHWIN (2011)

Development of Advanced Shearography System for On-Site Inspection of Wind Turbine Blades

Read More  

POSTO (2011)

Methodology and SW libraries for the design and development of GALILEO/EGNOS-based POSiTiOning applications for smartphones

Read More  

HYDRO-COAT (2009)

Novel high-pressure water hydraulic equipment for application in the construction and mining sector

Read More