1 / 13

Faculty of Medicine and Health Sciences Microbiology Lab Second semester 2013-2014

Faculty of Medicine and Health Sciences Microbiology Lab Second semester 2013-2014 prepared by: Mohammad Al-Qadi E-mail: m.qadi@najah.edu. Bacterial Identification: biochemical tests (1). Lab # 11. Introduction. -when you work in microbiology you mostly deal with Unknown microbes

dane-keller
Télécharger la présentation

Faculty of Medicine and Health Sciences Microbiology Lab Second semester 2013-2014

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Faculty of Medicine and Health Sciences Microbiology Lab Second semester 2013-2014 prepared by: Mohammad Al-Qadi E-mail: m.qadi@najah.edu

  2. Bacterial Identification: biochemical tests (1) Lab # 11

  3. Introduction -when you work in microbiology you mostly deal with Unknown microbes -Identification of unknown microbes can be achieved by using our knowledge about: *properties and characteristics of media available ( selective, differential, enriched etc.) *Growth characteristics *Staining *Biochemical tests to confirm identification and finalize the result.

  4. Introduction Biochemical tests (enzymatic) can be classified into two categories: A) one specific enzyme B) Complete metabolic pathway (several enzymes) 1. Carbohydrate oxidation and fermentation 2. Amino acid degradation 3. Single substrate utilizations Catalase , oxidase , indole ,urease ,PYR, hippurate hydrolysis, etc

  5. Catalase -This test is used to identify organisms that produce the enzyme, catalase. -This enzyme detoxifies hydrogen peroxide by breaking it down into water and oxygen gas (bubbles). H2O2 + catalase H2O + O2 -Key identification for Gramm+ vecocci Staphylococci – positive Streptococci – negative

  6. Coagulase -This test is used to identify organisms that produce the enzyme, coagulase. -This enzyme converts fibrinogen to fibrin (plasma clot) -Detected by slide (bound) or test tube (free or clumbing factor) method. -Firstly do slide method. If negative confrim using tube method. -In tube method read result after 1-4hoursat 37 C if negative incubate at room temperature over night

  7. Coagulase Slide test (bound or clumping factor) Tube test (free coagulase) If negative confirm by tube method check tubes at ½, 1, 2 & 4 hrs and over night • Result • If the organism is has coagulase it will clump the plasma. • If the organism does not have coagulase it will not clump the plasma

  8. Oxidase -This test (CytochromeOxidase test) is used to identify organisms that produce the enzyme, Oxidase. -This enzyme Detect by adding few drops of colorless oxidase reagent Colonies turn deep purple in color (positive) • (Oxidasescatalyse electron transport between substrates acting as electron donors in the bacterium and tetramethyl-p-phenylenediamine OR dimethyl-p-phenylenediamine - a redox dye present as the hydrochloride or oxalate salt The dye is reduced to a deep violet-blue colour in the presence of oxidase enzymes)

  9. Oxidase It uses disks impregnated with a reagent such as N,N,N′,N′-tetramethyl-p-phenylenediamine (TMPD) or N,N-Dimethyl-p-phenylenediamine (DMPD), which is also a redox indicator. Note the purple to dark purple color after the colonies have been added to filter paper moistened with oxidase reagent. • Positive control: Pseudomonas aeruginosa • Negative control: Enterobactericia

  10. Methyl Red/VogesProskauer (MR/VP) • These tests are used to determine what end products result when the test organism degrades glucose. • MR-VP media contains glucose and peptone (Methyl red & Potassium Hydroxide both used as indicators) . • All enterics oxidize glucose for energy; however the end products vary depending on bacterial enzymes • Inoculate 2 glucose broths with inoculating loop. After24-48 hours of incubation, add a few drops of MR to one tube, and VP reagents to the other tube. • Both tests are used to help differentiate species of the family Enterobacteriaceae. • MR—tests for acid end products from glucose fermentation. • VP—tests for acetoin (Acetyl methyl carbinol) production from glucose fermentation.

  11. MR/VP • Reading Results: • MR a positive result is red (indicating pH below 6) and a negative result is yellow (indicating no acid production) • VP a positive result is red after VP reagents are added (indicating the presence of acetoin) and a negative result is no color change. • This colour may take 20 to 30 minutes to develop. E. coli does not produce acetyl methyl carbinol, but Enterobacterand Klebsiellado. Methyl Red: left – and right + VP: left + and right –

  12. Good Luck

More Related