TECHNOLOGY OF RECOMBINANT DNA
cod. 07373

Academic year 2016/17
3° year of course - First semester
Professor
Angelo BOLCHI
Academic discipline
Biologia molecolare (BIO/11)
Field
Discipline biomolecolari
Type of training activity
Characterising
47 hours
of face-to-face activities
6 credits
hub: PARMA
course unit
in - - -

Learning objectives

The course aims to introduce the basic molecular biology techniques used in gene isolation and cloning, and in expression of recombinant proteins in a bacterial host

Prerequisites

No

Course unit content

The course will address the following topics:
1. Restriction enzymes • Methylation of DNA • DNA ligase • DNA polymerase • Reverse transcriptase (RNA dependent DNA polymerase) • Terminal Transferase • T4 Polynucleotide kinase • RNA polymerase • Alkaline phosphatase • Nuclease
2. Purification of DNA and RNA • Extraction with Phenol, Phenol-Chloroform, Chloroform • DNA precipitation with alcohol and drying • DNA resuspension in TE or water • Determination of the DNA concentration and purity
3. Bacterial growth • Media • Genotype • Conservation and propagation of bacteria
4. Bacterial plasmids • Replication and Incompatibility • Mobility • Selection Markers • Development of plasmids as cloning vectors and purification • Extraction of plasmid DNA from bacteria • Digestion with restriction enzymes • Purification of the digestion products • Strategies of ligation • Ligation of exogenous DNA into a plasmid vector • Bacterial Transformation • Identification of bacterial colonies containing recombinant plasmid of interest • Identification of possible results of ligation and transformation • Controls on ligation and transformation • Amplification and storage of clones and plasmid libraries
5. Bacteriophage lambda • Molecular biology of bacteriophage lambda • Construction of vectors based on bacteriophage lambda •Titration of bacteria • Titration of phages • Extraction and purification of phage DNA • Preparation of recombinant phage • Infection and plaques isolation • Identification of recombinant phages • Amplification and storage of clones or phage libraries
6. Characteristics of cosmid • Construction of cosmid genomic libraries • Amplification and storage of cosmid clones or cosmid libraries
7. Single-stranded filamentous bacteriophages • Molecular biology of filamentous bacteriophages • Cloning in the intergenic region of the RF • Processing and plaque formation • Identification of plaques containing recombinant phage • Extraction and purification of phage DNA • Multiplication of phage in liquid media • DNA Purification from phage • Amplification and conservation of the phage clones
8. Phagemids • Phagemid features • Cloning in the phagemid • Production of single-stranded DNA by helper phage • Construction of cDNA libraries in phagemid • lambda-ZAP • Cloning and recovery of the plasmid
9. Gel electrophoresis • Agarose gel electrophoresis • Recovery of DNA from gels • Denaturing agarose gel (alkaline, formaldehyde) • Electrophoresis on non-denaturing and denaturing polyacrylamide gel • Autoradiography • Recovery of DNA from the gel. • Analysis and cloning of eukaryotic genomic DNA • Isolation of genomic DNA • DNA Fragmentation of eukaryotic genomic • Complexity of a genomic library • High capacity vectors used for genomic libraries • Screening of a genomic library
10. Extraction and purification of RNA • Preparation of materials and solutions used in the RNA extraction • Traditional methods of extraction • Separation of Poly (A) + RNA
11. Construction and analysis of cDNA libraries • Complexity of a cDNA library • Synthesis of the first strand of cDNA • Synthesis of the second strand of the cDNA • Cloning of cDNA into a vector • Screening by hybridization of nucleic acids
12. PCR • Essential components of PCR • PCR thermal Phases • Design of primers • Problem of contamination • Hot Start • Analysis with gel electrophoresis • Cloning • Nested PCR • Amplicon • • Long PCR mutagenesis • Reverse Transcriptase-PCR (RT-PCR) • Touchdown PCR
13. Sequencing method of Maxam and Gilbert • Sequencing method of Sanger • sequencing of long DNA fragments and whole genomes
14. Expression in bacteria of a recombinant protein

Full programme

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Bibliography

Dai geni ai genomi - Dale, von Schantz - EdiSES
Analisi dei geni e genomi - Richard J.Reece - EdiSES
Ingegneria genetica. Principi e tecniche. S.Primrose et al. - Zanichelli
DNA Ricombinante - J.D.Watson et al. - Zanichelli

Teaching methods

Lecture

Assessment methods and criteria

Written examination

Other information

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2030 agenda goals for sustainable development

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Contacts

Toll-free number

800 904 084

Student registry office

T.+39 0521 905116
E. segreteria.scienze@unipr.it

Quality assurance office

Education manager 

Roberta Pagani
T. +39 0521 905613 -  +39 0521 905555
E. servizio didattica.scvsa@unipr.it
E. del manager roberta.pagani@unipr.it

 

President of the degree course

Valeria Rossi

Deputy President of the degree course 

Alessandra Mori

Faculty advisor

Antonella Bachiorri

Career guidance delegate

Anna Torelli

Quality assurance manager

Prof.ssa Alessandra Mori

Internships

Paolo Lunghi