PřF:Bi6721c Spec.Meth.Microorg.Anal.I.-pr. - Course Information
Bi6721c Special Methods of Microorganisms Analysis I. - practical course
Faculty of ScienceSpring 2009
- Extent and Intensity
- 0/3/0. 3 credit(s). Type of Completion: z (credit).
- Teacher(s)
- doc. RNDr. Alena Španová, CSc. (seminar tutor)
doc. Ing. Bohuslav Rittich, CSc. (seminar tutor)
RNDr. Aleš Kovařík, CSc. (seminar tutor) - Guaranteed by
- doc. Ing. Bohuslav Rittich, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. Ing. Bohuslav Rittich, CSc. - Timetable of Seminar Groups
- Bi6721c/01: Wed 8:00–10:50 Bpb,02012, B. Rittich, A. Španová
Bi6721c/02: Wed 11:00–13:50 Bpb,02012, B. Rittich, A. Španová - Prerequisites
- NOW( Bi6721 Spec. Meth. Microorg. Anal. I. )
The course is for the students which will know to performe the basic noncultivation microbiological method polymerase chain reaction. - Course Enrolment Limitations
- The course is also offered to the students of the fields other than those the course is directly associated with.
- fields of study / plans the course is directly associated with
- General Biology (programme PřF, B-BI, specialization Microbiology)
- General Biology (programme PřF, M-BI, specialization Microbiology)
- General Biology (programme PřF, N-BI, specialization Microbiology)
- Course objectives
- Safety of work in mikrobiology laboratory. Basic procedures with DNA work: isolation and purification of bacterial DNA, DNA precipitation using ethanol, estimation of DNA concentration and purity. Agarose gel electrophoresis of bacterial DNA, DNA visualisation and gel documentation. Preparation of PCR mixture for specific amplification of DNA of Salmonella and performance of PCR. Detection of PCR product using agarose gel electrophoresis and estimation of the length of PCR product. Estimation of PCR sensitivity. PCR with crude cell lysate after immunomagnetic separation (IMS) of cells Salmonella. This practical course is supplemented by course Bi6721.
At the end of this course, students should be able to practically carried out the basic polymerase chain reaction. - Syllabus
- 1. Safety of work in microbiology laboratory. Pipeting of small volumes of solvents using pippetmans. Preparation of media for cultivation of bacteria.
- 2. Preparation of Salmonella Typhimurium LB5000 cells for isolation of bacterial DNA. Cell lysis.
- 3. DNA deproteination using phenol extraction. Precipitation of DNA with ethanol.
- 4. Estimation of DNA integrity using agarose gel electrophoresis of isolated DNA. DNA visualisation and gel documentation.
- 5. Estimation of DNA concentration and purity. Preparation of DNA in concentration suitable for PCR.
- 6. The work flow in PCR laboratory. Preparation of PCR mixture for specific amplification of gene Salmonella using purified DNA as DNA matrix. PCR reaction.
- 7. Detection of PCR product using agarose gel electrophoresis.
- 8. Estimation of amplicon length using known standards.
- 9. Preparation of PCR mixture from trude cell lysates. Positive and negative controls. PCR and detection of PCR produkt.
- 10.Imunomagnetic separation (IMS) of cells Salmonella. IMS-cultivation (IMS-CM) of cells Salmonella. IMS-polymerase chain reaction (IMS-PCR) with cells Salmonella. Estimation of PCR sensitivity.
- 11.I PCR products detection using agarose gel electropjoresis.
- 12. and 13. Identification of Salmonella cells in unknown sample using PCR.
- 14. Evaluation of protocols.Test.
- Literature
- F.Sambrook and D.W. Russell Molecular Cloning. A Laboratory Manual. 3rd ed. Cold Spring Harbor Laboratory Press. 2001
- Assessment methods
- Training is enclosed by test.
- Language of instruction
- Czech
- Follow-Up Courses
- Further comments (probably available only in Czech)
- The course is taught annually.
Information on course enrolment limitations: Přednost mají posluchači specializace mikrobiologie.
- Enrolment Statistics (Spring 2009, recent)
- Permalink: https://is.muni.cz/course/sci/spring2009/Bi6721c