Biodeep May 12-14, 2003 “Nature has more imagination than our dreams”

Slides:



Advertisements
Similar presentations
Recombinant DNA Technology
Advertisements

Ch. 2A: How Do You Begin to Clone a Gene?. Learning goals Describe the characteristics of plasmids Explain how plasmids are used in cloning a gene Describe.
Aulani "GE" Presentation 3 Gene Cloning Aulanni’am Biochemistry Laboratory Chemistry Department Brawijaya University
Bioinformatics Student host Chris Johnston Speaker Dr Kate McCain.
Cloning:Recombinant DNA
Making, screening and analyzing cDNA clones Genomic DNA clones
Plasmid purification lab
Definition The terms recombinant DNA technology, DNA cloning, molecular cloning, or gene cloning all refer to the same process: the transfer of a DNA.
Genomic DNA & cDNA Libraries
Biotechnology Read textbook sections 20.1 & 20.2 on your own Draw 10 boxes to complete the following notes Turn into the purple box when you are done.
Gene knockout Lecturer : Du Shengyang January
Genetic Engineering Do you want a footer?.
Introduction to biotechnology Haixu Tang School of Informatics.
Gene Technology Section 1: Genetic Engineering
© 2006 W.W. Norton & Company, Inc. DISCOVER BIOLOGY 3/e 1 Manipulation of DNA Selective breeding has manipulated DNA f/ eons  Domesticated animals demonstrate.
Molecular Identification Methods Confirmation of identity for commonly used laboratory strains should ideally be done at the level of genotypic analysis’…...
Chapter 13. The Impact of Genomics on Antimicrobial Drug Discovery and Toxicology CBBL - Young-sik Sohn-
Diversity of uncultured candidate division SR1 in anaerobic habitats James P. Davis Microbial & Molecular Genetics Oklahoma State University.
Screening a Library Plate out library on nutrient agar in petri dishes. Up to 50,000 plaques or colonies per plate.
Library screening Heterologous and homologous gene probes Differential screening Expression library screening.
Microbial Biotechnology Philadelphia University
Recombinant DNA Technology Prof. Elena A. Carrasquillo Chapter 4 Molecular Biotechnology Lecture 4.
Molecular Detection of Karenia spp. in the Mid-Atlantic Kathryn J. Coyne 1, Edward Whereat 1, Muns Farestad 1, Jennifer Torora 1, Lauren Salvitti 1 and.
Lab 8 Goals and Objectives: Do not disrupt BHI broths: need to see surface growth. Do not shake FTM tubes Make all Gram stain smears from broth & plates.
DNA alphabet DNA is the principal constituent of the genome. It may be regarded as a complex set of instructions for creating an organism. Four different.
FINISHING WORKSHOP APRIL 2008 CHROMOSOME 7 THE FRENCH CONTRIBUTION TG216 TG438 T1112 T1355 T1328 T1428 T1962 T1414 T1497 T0676 TM18 CT54 T0966 T0731 TM15.
CoNISMa, Consorzio Nazionale Interuniversitario Scienze del Mare Partner 1c DISTAM Università degli Studi di Milano Daniele Daffonchio Tullio Brusa Sara.
FLEXGene Repository Applications. Exploiting FLEXGene Genes FLEXGene Clones Expression Clones Proteins Protein Expression Localization Interaction Functional.
_________________________________________________________
Section 1 Genetic Engineering Basic Steps of Genetic Engineering Genetic Engineering Genetic engineers manipulate DNA for practical purposes. Restriction.
Genetic Engineering 1 Lecture 18 Pages
CoNISMa, Consorzio Nazionale Interuniversitario Scienze del Mare Partner 1c DISTAM Università degli Studi di Milano Daniele Daffonchio Tullio Brusa Sara.
DNA LIBRARIES Dr. E. What Are DNA Libraries? A DNA library is a collection of DNA fragments that have been cloned into a plasmid and the plasmid is transformed.
Genetic Engineering Genetic engineering is also referred to as recombinant DNA technology – new combinations of genetic material are produced by artificially.
Molecular Biology II Lecture 1 OrR. Restriction Endonuclease (sticky end)
Lesson 2 Lecture: Identification of clones of interest
Molecular Cloning.
Plasmids that contain l cos sites.
The two-hybrid system – why?
BIODEEP MEETING - Marseille, April 2002 Workpackages 4 and 5 - Fabienne MOREL, Sam DUKAN Objectives : isolation of new strains from DHABs Interface.
1 9/21/2010 Microbial Bioinsecticide Bacillus thuringiensis Dr. Aris Tri Wahyudi Department of Biology Bogor Agricultural University 2008 Microbial Insecticide.
Plan A Topics? 1.Making a probiotic strain of E.coli that destroys oxalate to help treat kidney stones in collaboration with Dr. Lucent and Dr. VanWert.
Molecular Cloning. Definitions   Cloning :   Obtaining a piece of DNA from its original source (Genome) and introducing it in a DNA vector   Sub-cloning:
BSL2016 / 2018 LEC 8 Genomic Libraries (1) What is a genomic library and why is it important? How does a genomic library differ from a cDNA library? cDNA.
REVIEW OF MOLECULAR GENETICS DR. EDELBERG. Genes, DNA, & Chromosomes.
Slide 1 Insert your own content.. Slide 2 Insert your own content.
Lecture 3 – Selection of Recombinants & clone analysis The white colonies will all be recombinants, but only one of these many colonies will contain the.
1 General Biology Chapter 11 Gene Technology. 2 Genetic Engineering Recombinant DNA is made when a DNA fragment is put into the DNA of a vector Gel electrophroesis.
Abira Khan.  The first stage in the screening for microorganisms of potential industrial application  Involves obtaining either pure or mixed cultures.
Metagenomics (Environmental Genomics, Ecogenomics, Community Genomics) Dr. Bhavesh Patel Principal V.P. and R.P.T.P. Science College Vallabh Vidyanagar,
Topics to be covers Basic features present on plasmids
E.Coli AS MODERN VECTOR.
Partner 1c CoNISMa, Consorzio Nazionale Interuniversitario Scienze del Mare DISTAM Università degli Studi di Milano Daniele Daffonchio Tullio Brusa Sara.
Seminar on :- Constructing Contigs Sequencing
Cloning DNA Sequences that Encode Eukaryotic Protein
Identification of nifH and nodC genes from Rhizobium aegyptiacum
BIODEEP-WP4 BIODEEP-WP5 Andrea Sass , Terry McGenity
Yeast Two-Hybrid Screening: The Principles
Unculturable Bacteria
Peter John M.Phil, PhD Atta-ur-Rahman School of Applied Biosciences (ASAB) National University of Sciences & Technology (NUST)
Vav‐1 gene‐targeting strategy.
Microbiology: A Systems Approach
Slide 1 Insert your own content.. Slide 1 Insert your own content.
Slide 1 Insert your own content.. Slide 1 Insert your own content.
Slide 1 Insert your own content.. Slide 1 Insert your own content.
Chapter 9 Molecular Genetic Techniques and Genomics
Volume 86, Issue 1, Pages (July 1996)
Scientometrics of Horizontal Gene Transfer Research during
E.Coli AS MODERN VECTOR.
Laurel L Lenz, Beverley Dere, Michael J Bevan  Immunity 
Presentation transcript:

Biodeep May 12-14, 2003 “Nature has more imagination than our dreams”

Contents l Strains and clones transferred l Microbial screening 3 Proteases 3 Esterases l Molecular screening l Biodeep Database l Communications l Conclusion

Strains transferred l Milan University (Dr. T. Brusa) 1. Strains studied means that we tried at least once to culture them 2. Strains cultured means strains that have been cultured in our lab (and therefor stored in collection) and can be used for future work

Strains transferred l Essex University (Dr. A. Sass) Anaerobic strains will be transfer soon 1. Strains studied means that we tried at least once to culture them 2. Strains cultured means strains that have been cultured in our lab (and therefor stored in collection) and can be used for future work 3. The 19 strains of the 1 st batch which could not be cultured in our lab have been sent a second time recently

Strains transferred l Messina University (Dr. G. D’auria) 1. Strains studied means that we tried at least once to culture them 2. Strains cultured means strains that have been cultured in our lab (and therefor stored in collection) and can be used for future work 3. See next slide 4. All the strains excepted the ones growing in P10 medium (petrol based medium)

Strains transferred to Protéus l Cultures from Univ. Messina 3 Enrichment cultures and pure strains 3 No synthetic media defined (from the water point of view) 3 We tried to grow the stains in a defined medium 3 The growth conditions defined for the 22 strains cultured in our lab are available

Strains transferred l LLM (Dr. F. Morel) 1. Strains studied means that we tried at least once to culture them 2. Strains cultured means strains that have been cultured in our lab (and therefor stored in collection) and can be used for future work

Strains transferred 1. Strains studied means that we tried at least once to culture them 2. Strains cultured means strains that have been cultured in our lab and can be used for future work l Review

Clones transferred l clones from TUB (Dr. P. Golyshin) 3 3 genomic fragments encoding 3 different esterases (oil2, oil7 and oil8) 3 Corresponding sequences have been provided with the genomic fragments 3 subcloning of oil8 in progress for shuffling purposes

Microbial screening l Extracellular proteases using skim milk (0.2%) screening assay l Examples P 1600 P 1975 P 1972 After 3 days at 25°C After 2 days at 25°C

l Review (aerobes) Results

l Taxonomic position according to the studies done by each Biodeep partners

Microbial screening l Esterases l Principle of the CLIPS-O substrates R = C 2 H 5 C 9 H 19

Preliminary Results l Review (aerobes)

Molecular screening l Proteases from strain P 1972 (Alteromonas sp.) l Genomic library construction : partial restriction using Sau 3A I l Inserts size ranging from 2 to 5 kb l Quality control : less than 10% of empty clones

Screening results l Library screening clones screened 36 (confirmed) positive hits l Expression (preliminary results) Negative control Clone 9 Clone 10

Biodeep database l Protéus Design of the data sheet model Model sent to University of Milano on February, 2002 l University of Milano Design of the database

Biodeep database

These 2 forms have to be filled by each partner for each strain

Biodeep database l Data form to be completed by each partner For the isolated strains And update of the form as soon as new information and results are obtained l Data to be transferred to Protéus l Protéus will transfer all the data to University of Milano l Integration of all the data by University of Milano

Biodeep database l Up to now, we received from University of Marseille 20 forms filled.

Communications l Our industrial partners l Congress : 3 EMBO workshop (France) 3 INFORMEX (USA) 3 BioMarket 2002 (England) 3 BIOTECNICA Business Forum (Germany) 3 Global Venture Forum (Japan)

Conclusions and Outlook l Current status of the Biodeep collection : 310 strains l Identification of strains producing esterases and extracellular proteases l Protease gene(s) from strain P 1972 (Alteromonas sp.) already cloned (sequencing in progress) l Database ready to be filled? l New strains and bulk DNA?

Timetable of future activities

…Thanks for your attention.

Environmental libraries