SlideShare a Scribd company logo
1 of 22
Biochemical Activities of Microorganisms
Sercan Güloğlu
19-21 December 2018
Voges Proskauer
1. Take 1 mL to a new tube.
2. Add 0,5 mL Barrit’s A solution.
3. Add 0,3 mL Barrit’s B solution.
4. Shake vigorously every 20 sec for a minute. Wait for 1-2 hours for the results.
• Red Color: acethylmethyl carbinol presence which means the production
of 2,3 butanediol from pyruvic acid.
2
Indole Methylred Voges-proskauer i Citrate
3
Methyl Red
1. Take 2 mL to a new tube
2. Add 5 drops of methyl red
• Red color: Acidic. (Mixed acid production
• Yellow color: Alkaline (No mixed acid production).
Indole Methylred Voges-proskauer i Citrate
Gelatin Hydrolysis
• Put your tubes into the fridge.
• Make sure they are melt before putting.
4
Nitrogen Metabolism
Carbon Metabolism
Starch Hydrolysis
Flood surface of the agar with iodine
Dark blue : No amylase activity.
Clear zone around colonies: Alpha & Beta amylase activity.
Red complex : Alpha amylase activity only (amylopectin remains intact).
5
Carbon Metabolism
6
Phenol Red Broth (Glucose & Lactose)
1. Check the bacteria growth (do not mix the tube) (maybe in a form of precipitation)
2. Check if there is any bubble in the Durham tube (Gas production)
3. Check the color of the broth:
– Yellow: Acidic
– Red: Alkaline
7
Indole Production (Tryptone broth)
1. Check the bacterial growth.
2. Add 10 drops of Kovac’s reagent and mix well in your hand.
• Red Color: Indole production.
Nitrogen Metabolism
Urea Utilization
1. Check bacterial growth.
2. Observe the color of the slant.
• Pink-Red Color: Urease activity. NH3 production increased the pH.
• Yellow Color: No urease activity.
8
Nitrogen Metabolism
Gelatin Hydrolysis
Get your tubes from the fridge.
1. Observe vertical growth of bacteria (growth control).
2. Observe liquefaction by holding tube inclined.
– Liquid: Gelatinase activity.
– No liquid: No gelatinase activity.
9
Nitrogen Metabolism
Nitrate Reduction
1. Check bacterial growth.
2. Check the bubble formation in the Durham tube.
• Gas production: All enzymes are active.
• No gas production: Not all enzymes are active.
10
Nitrogen Metabolism
3. Take 2 mL to a clean test tube.
4. 2 drops of Sulfanilic acid then 1 drop dimethyl-alpha-naphtylamine(for nitrite detection).
• Red color: Reduction of nitrate into nitrite.
• No color: There is no nitrite in the medium.
Nitrate Reduction(cont’d)
5. Add a pinch of zinc dust to your original culture.
• Red color: Unreduced Nitrate present in the culture.
• No color: Nitrate is reduced (Nitrate reductase is active).
11
Nitrogen Metabolism
12
Indole Methylred Voges-proskauer i Citrate
Indole Production (Tryptone broth)
Use the data from the indole production test previously observed.
Citrate Utilization
1. Observe the color change.
• Blue: Citrate utilization as a carbon source.
• Green: Citrate is not a Carbon source for corresponding organism.
13
Indole Methylred Voges-proskauer i Citrate
14
Litmus Milk
1. Check the acid curd formation (insoluble complex of calcium and casein).
• Purple to pink (curd formation).
2. Check for alkaline reaction.
• Blue: Alkaline formation.
• Purple: No alkaline formation.
Multiple Test Media
15
Litmus Milk (cont’d)
3. Check for the peptonization (digestion of milk protein casein by proteases).
• Reduction in curd size and formation of brownish liquid.
4. Check for litmus color change.
• White color: reduction of litmus.
Multiple Test Media
16
Litmus Milk (cont’d)
5. Check for the gas formation (furrow formation in the curd).
• Furrows: gas production.
6. Check for ropiness (Immerse a loop into the medium and slowly remove it.
Observe if there is any string).
• String: indication of ropiness.
Multiple Test Media
17
Triple Sugar Iron (TSIA)
1. Check for the colors of slant and butt seperately.
• Yellow butt: glucose utilization.
• Red color on the slant: only glucose fermenters.
• Yellow slant: organism can also ferment lactose and/or sucrose.
2. Check for the gas formation.
3. Check for the H2S formation(detected by FeS).
• Black colored agar: H2S formation.
Multiple Test Media
Sulfide Indole Motility (SIM)
1. Check for the color of your culture.
• Dark color: hydrogen sulfide production.
2. Check for the diffusion of the colonies.
• Diffused color: motile organism.
3. Add 10 drops of Kovac’s reagent. Observe the color change.
• Pink color: Indole production.
18
Multiple Test Media
19
REPORTS
20
Positive outcome:
Our starch agar experiment results showed that our organism can hydrolyse the starch. Upon
addition of iodine on the agar, clearing occured as whitish color around the colonies which is an
indicator of both alpha and beta amylase activity. It has been previously shown that Bacillus subtilis
gives positive reaction clearing colony around [1,2]. Therefore, this outcome supports that our
unknown bacterium might be Bacillus subtilis.
Negative outcome
Our starch agar experiment results showed that our organism cannot hydrolyse the starch. Upon
addition of iodine on the agar, nothing changed around the colonies which is an indicator of no
amylase activity. It has been previously shown that Escherichia coli gives negative reaction on
starch agar test [3]. Therefore, this outcome supports that our unknown bacterium might be
Escherichia coli.
In-text reference
In-text reference
21
• 4 pages (maximum) of reports will be arranged as follows:
• Cover page: Your section and group number. Write your group members as well.
• Maximum 2 pages of discussion (1 page is preferred).
• 1 separate page for the reference list. (Check for the reference tools for correct reference formatting).
• Font: Arial---10 puncta---Centered text---Word format
• Mail your reports to: guloglu.sercann@gmail.com
• No questions about any test’s evaluation will be answered !!!
• You can use websites as a reference. However, scientific article references will receive extra points.
• You have 7 days for report submission.
• Earlier report submissions will get you extra 5 points per day up to 4 days (+20 points in total)
• Later report submissions will take away your 10 points per day.
22
• Grading of the reports:
Points
Cover page 5
Introduction pragraph (2-3 sentences) 5.4
Evaluation of 11 different tests
(11 separate paragraphs)
5.4 (each paragraph)
59 (total)
Conclusion paragraph 5.4
References
(correct formatting & correct information)
10
Language & text formatting 5
Correct prediction of the culture 10
Total 100
Scientific article reference +2 (per article)
Earlier report submission
+5 (per day)
+20 (maximum)
Later report submission -10 (per day)

More Related Content

Similar to Biochemical tests 2nd week

PPT_B.Voc. MLT_Sem 3_MLT 7_Ch 16_v 1.3_Shweta.pptx
PPT_B.Voc. MLT_Sem 3_MLT 7_Ch 16_v 1.3_Shweta.pptxPPT_B.Voc. MLT_Sem 3_MLT 7_Ch 16_v 1.3_Shweta.pptx
PPT_B.Voc. MLT_Sem 3_MLT 7_Ch 16_v 1.3_Shweta.pptx
Adityasonawane32
 

Similar to Biochemical tests 2nd week (20)

Aniline qualitative analysis
Aniline qualitative analysisAniline qualitative analysis
Aniline qualitative analysis
 
biochemicalreactionsnew-190412162327.pdf
biochemicalreactionsnew-190412162327.pdfbiochemicalreactionsnew-190412162327.pdf
biochemicalreactionsnew-190412162327.pdf
 
Biochemical reactions new
Biochemical reactions newBiochemical reactions new
Biochemical reactions new
 
BIOCHEM CARBOHYDRATES
BIOCHEM CARBOHYDRATESBIOCHEM CARBOHYDRATES
BIOCHEM CARBOHYDRATES
 
biochemical test for identification of bacteria.pptx
biochemical test for identification of bacteria.pptxbiochemical test for identification of bacteria.pptx
biochemical test for identification of bacteria.pptx
 
Biochemistry Practicals.pptx
Biochemistry Practicals.pptxBiochemistry Practicals.pptx
Biochemistry Practicals.pptx
 
Lab discussion
Lab discussionLab discussion
Lab discussion
 
List of biochemical tests
List of biochemical testsList of biochemical tests
List of biochemical tests
 
Carbohydrate practical
Carbohydrate practicalCarbohydrate practical
Carbohydrate practical
 
PPT_B.Voc. MLT_Sem 3_MLT 7_Ch 16_v 1.3_Shweta.pptx
PPT_B.Voc. MLT_Sem 3_MLT 7_Ch 16_v 1.3_Shweta.pptxPPT_B.Voc. MLT_Sem 3_MLT 7_Ch 16_v 1.3_Shweta.pptx
PPT_B.Voc. MLT_Sem 3_MLT 7_Ch 16_v 1.3_Shweta.pptx
 
Medical Microbiology Laboratory (biochemical tests - ii)
Medical Microbiology Laboratory (biochemical tests - ii)Medical Microbiology Laboratory (biochemical tests - ii)
Medical Microbiology Laboratory (biochemical tests - ii)
 
carbohydrate_i.pdf
carbohydrate_i.pdfcarbohydrate_i.pdf
carbohydrate_i.pdf
 
Isolation of Carbohydrates - Experiment no. 4
Isolation of Carbohydrates - Experiment no. 4Isolation of Carbohydrates - Experiment no. 4
Isolation of Carbohydrates - Experiment no. 4
 
Isolation of l asparaginase
Isolation of l asparaginaseIsolation of l asparaginase
Isolation of l asparaginase
 
Urine Testing for Detection of presence of glucose and proteins
Urine Testing for Detection of presence of glucose and proteinsUrine Testing for Detection of presence of glucose and proteins
Urine Testing for Detection of presence of glucose and proteins
 
Chapter 10 Biochemical tests.pptx bacteriology
Chapter 10 Biochemical tests.pptx bacteriologyChapter 10 Biochemical tests.pptx bacteriology
Chapter 10 Biochemical tests.pptx bacteriology
 
Class-6, Identification of microbes.pptx
Class-6, Identification of microbes.pptxClass-6, Identification of microbes.pptx
Class-6, Identification of microbes.pptx
 
Qualitative test for proteins
Qualitative test for proteinsQualitative test for proteins
Qualitative test for proteins
 
Medical Microbiology Laboratory (biochemical tests - i)
Medical Microbiology Laboratory (biochemical tests - i)Medical Microbiology Laboratory (biochemical tests - i)
Medical Microbiology Laboratory (biochemical tests - i)
 
MICROBIOLOGY biochemical test detailed.pptx
MICROBIOLOGY biochemical test detailed.pptxMICROBIOLOGY biochemical test detailed.pptx
MICROBIOLOGY biochemical test detailed.pptx
 

Recently uploaded

CYTOGENETIC MAP................ ppt.pptx
CYTOGENETIC MAP................ ppt.pptxCYTOGENETIC MAP................ ppt.pptx
CYTOGENETIC MAP................ ppt.pptx
Cherry
 
Pteris : features, anatomy, morphology and lifecycle
Pteris : features, anatomy, morphology and lifecyclePteris : features, anatomy, morphology and lifecycle
Pteris : features, anatomy, morphology and lifecycle
Cherry
 
COMPOSTING : types of compost, merits and demerits
COMPOSTING : types of compost, merits and demeritsCOMPOSTING : types of compost, merits and demerits
COMPOSTING : types of compost, merits and demerits
Cherry
 
(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...
(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...
(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...
Scintica Instrumentation
 
Reboulia: features, anatomy, morphology etc.
Reboulia: features, anatomy, morphology etc.Reboulia: features, anatomy, morphology etc.
Reboulia: features, anatomy, morphology etc.
Cherry
 
POGONATUM : morphology, anatomy, reproduction etc.
POGONATUM : morphology, anatomy, reproduction etc.POGONATUM : morphology, anatomy, reproduction etc.
POGONATUM : morphology, anatomy, reproduction etc.
Cherry
 
THE ROLE OF BIOTECHNOLOGY IN THE ECONOMIC UPLIFT.pptx
THE ROLE OF BIOTECHNOLOGY IN THE ECONOMIC UPLIFT.pptxTHE ROLE OF BIOTECHNOLOGY IN THE ECONOMIC UPLIFT.pptx
THE ROLE OF BIOTECHNOLOGY IN THE ECONOMIC UPLIFT.pptx
ANSARKHAN96
 

Recently uploaded (20)

CYTOGENETIC MAP................ ppt.pptx
CYTOGENETIC MAP................ ppt.pptxCYTOGENETIC MAP................ ppt.pptx
CYTOGENETIC MAP................ ppt.pptx
 
Genome organization in virus,bacteria and eukaryotes.pptx
Genome organization in virus,bacteria and eukaryotes.pptxGenome organization in virus,bacteria and eukaryotes.pptx
Genome organization in virus,bacteria and eukaryotes.pptx
 
Pteris : features, anatomy, morphology and lifecycle
Pteris : features, anatomy, morphology and lifecyclePteris : features, anatomy, morphology and lifecycle
Pteris : features, anatomy, morphology and lifecycle
 
COMPOSTING : types of compost, merits and demerits
COMPOSTING : types of compost, merits and demeritsCOMPOSTING : types of compost, merits and demerits
COMPOSTING : types of compost, merits and demerits
 
Fourth quarter science 9-Kinetic-and-Potential-Energy.pptx
Fourth quarter science 9-Kinetic-and-Potential-Energy.pptxFourth quarter science 9-Kinetic-and-Potential-Energy.pptx
Fourth quarter science 9-Kinetic-and-Potential-Energy.pptx
 
GBSN - Microbiology (Unit 5) Concept of isolation
GBSN - Microbiology (Unit 5) Concept of isolationGBSN - Microbiology (Unit 5) Concept of isolation
GBSN - Microbiology (Unit 5) Concept of isolation
 
TransientOffsetin14CAftertheCarringtonEventRecordedbyPolarTreeRings
TransientOffsetin14CAftertheCarringtonEventRecordedbyPolarTreeRingsTransientOffsetin14CAftertheCarringtonEventRecordedbyPolarTreeRings
TransientOffsetin14CAftertheCarringtonEventRecordedbyPolarTreeRings
 
(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...
(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...
(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...
 
Plasmid: types, structure and functions.
Plasmid: types, structure and functions.Plasmid: types, structure and functions.
Plasmid: types, structure and functions.
 
Molecular phylogeny, molecular clock hypothesis, molecular evolution, kimuras...
Molecular phylogeny, molecular clock hypothesis, molecular evolution, kimuras...Molecular phylogeny, molecular clock hypothesis, molecular evolution, kimuras...
Molecular phylogeny, molecular clock hypothesis, molecular evolution, kimuras...
 
Reboulia: features, anatomy, morphology etc.
Reboulia: features, anatomy, morphology etc.Reboulia: features, anatomy, morphology etc.
Reboulia: features, anatomy, morphology etc.
 
Understanding Partial Differential Equations: Types and Solution Methods
Understanding Partial Differential Equations: Types and Solution MethodsUnderstanding Partial Differential Equations: Types and Solution Methods
Understanding Partial Differential Equations: Types and Solution Methods
 
Method of Quantifying interactions and its types
Method of Quantifying interactions and its typesMethod of Quantifying interactions and its types
Method of Quantifying interactions and its types
 
POGONATUM : morphology, anatomy, reproduction etc.
POGONATUM : morphology, anatomy, reproduction etc.POGONATUM : morphology, anatomy, reproduction etc.
POGONATUM : morphology, anatomy, reproduction etc.
 
Concept of gene and Complementation test.pdf
Concept of gene and Complementation test.pdfConcept of gene and Complementation test.pdf
Concept of gene and Complementation test.pdf
 
CONTRIBUTION OF PANCHANAN MAHESHWARI.pptx
CONTRIBUTION OF PANCHANAN MAHESHWARI.pptxCONTRIBUTION OF PANCHANAN MAHESHWARI.pptx
CONTRIBUTION OF PANCHANAN MAHESHWARI.pptx
 
Site specific recombination and transposition.........pdf
Site specific recombination and transposition.........pdfSite specific recombination and transposition.........pdf
Site specific recombination and transposition.........pdf
 
GBSN - Biochemistry (Unit 3) Metabolism
GBSN - Biochemistry (Unit 3) MetabolismGBSN - Biochemistry (Unit 3) Metabolism
GBSN - Biochemistry (Unit 3) Metabolism
 
Genome Projects : Human, Rice,Wheat,E coli and Arabidopsis.
Genome Projects : Human, Rice,Wheat,E coli and Arabidopsis.Genome Projects : Human, Rice,Wheat,E coli and Arabidopsis.
Genome Projects : Human, Rice,Wheat,E coli and Arabidopsis.
 
THE ROLE OF BIOTECHNOLOGY IN THE ECONOMIC UPLIFT.pptx
THE ROLE OF BIOTECHNOLOGY IN THE ECONOMIC UPLIFT.pptxTHE ROLE OF BIOTECHNOLOGY IN THE ECONOMIC UPLIFT.pptx
THE ROLE OF BIOTECHNOLOGY IN THE ECONOMIC UPLIFT.pptx
 

Biochemical tests 2nd week

  • 1. Biochemical Activities of Microorganisms Sercan Güloğlu 19-21 December 2018
  • 2. Voges Proskauer 1. Take 1 mL to a new tube. 2. Add 0,5 mL Barrit’s A solution. 3. Add 0,3 mL Barrit’s B solution. 4. Shake vigorously every 20 sec for a minute. Wait for 1-2 hours for the results. • Red Color: acethylmethyl carbinol presence which means the production of 2,3 butanediol from pyruvic acid. 2 Indole Methylred Voges-proskauer i Citrate
  • 3. 3 Methyl Red 1. Take 2 mL to a new tube 2. Add 5 drops of methyl red • Red color: Acidic. (Mixed acid production • Yellow color: Alkaline (No mixed acid production). Indole Methylred Voges-proskauer i Citrate
  • 4. Gelatin Hydrolysis • Put your tubes into the fridge. • Make sure they are melt before putting. 4 Nitrogen Metabolism
  • 5. Carbon Metabolism Starch Hydrolysis Flood surface of the agar with iodine Dark blue : No amylase activity. Clear zone around colonies: Alpha & Beta amylase activity. Red complex : Alpha amylase activity only (amylopectin remains intact). 5
  • 6. Carbon Metabolism 6 Phenol Red Broth (Glucose & Lactose) 1. Check the bacteria growth (do not mix the tube) (maybe in a form of precipitation) 2. Check if there is any bubble in the Durham tube (Gas production) 3. Check the color of the broth: – Yellow: Acidic – Red: Alkaline
  • 7. 7 Indole Production (Tryptone broth) 1. Check the bacterial growth. 2. Add 10 drops of Kovac’s reagent and mix well in your hand. • Red Color: Indole production. Nitrogen Metabolism
  • 8. Urea Utilization 1. Check bacterial growth. 2. Observe the color of the slant. • Pink-Red Color: Urease activity. NH3 production increased the pH. • Yellow Color: No urease activity. 8 Nitrogen Metabolism
  • 9. Gelatin Hydrolysis Get your tubes from the fridge. 1. Observe vertical growth of bacteria (growth control). 2. Observe liquefaction by holding tube inclined. – Liquid: Gelatinase activity. – No liquid: No gelatinase activity. 9 Nitrogen Metabolism
  • 10. Nitrate Reduction 1. Check bacterial growth. 2. Check the bubble formation in the Durham tube. • Gas production: All enzymes are active. • No gas production: Not all enzymes are active. 10 Nitrogen Metabolism 3. Take 2 mL to a clean test tube. 4. 2 drops of Sulfanilic acid then 1 drop dimethyl-alpha-naphtylamine(for nitrite detection). • Red color: Reduction of nitrate into nitrite. • No color: There is no nitrite in the medium.
  • 11. Nitrate Reduction(cont’d) 5. Add a pinch of zinc dust to your original culture. • Red color: Unreduced Nitrate present in the culture. • No color: Nitrate is reduced (Nitrate reductase is active). 11 Nitrogen Metabolism
  • 12. 12 Indole Methylred Voges-proskauer i Citrate Indole Production (Tryptone broth) Use the data from the indole production test previously observed.
  • 13. Citrate Utilization 1. Observe the color change. • Blue: Citrate utilization as a carbon source. • Green: Citrate is not a Carbon source for corresponding organism. 13 Indole Methylred Voges-proskauer i Citrate
  • 14. 14 Litmus Milk 1. Check the acid curd formation (insoluble complex of calcium and casein). • Purple to pink (curd formation). 2. Check for alkaline reaction. • Blue: Alkaline formation. • Purple: No alkaline formation. Multiple Test Media
  • 15. 15 Litmus Milk (cont’d) 3. Check for the peptonization (digestion of milk protein casein by proteases). • Reduction in curd size and formation of brownish liquid. 4. Check for litmus color change. • White color: reduction of litmus. Multiple Test Media
  • 16. 16 Litmus Milk (cont’d) 5. Check for the gas formation (furrow formation in the curd). • Furrows: gas production. 6. Check for ropiness (Immerse a loop into the medium and slowly remove it. Observe if there is any string). • String: indication of ropiness. Multiple Test Media
  • 17. 17 Triple Sugar Iron (TSIA) 1. Check for the colors of slant and butt seperately. • Yellow butt: glucose utilization. • Red color on the slant: only glucose fermenters. • Yellow slant: organism can also ferment lactose and/or sucrose. 2. Check for the gas formation. 3. Check for the H2S formation(detected by FeS). • Black colored agar: H2S formation. Multiple Test Media
  • 18. Sulfide Indole Motility (SIM) 1. Check for the color of your culture. • Dark color: hydrogen sulfide production. 2. Check for the diffusion of the colonies. • Diffused color: motile organism. 3. Add 10 drops of Kovac’s reagent. Observe the color change. • Pink color: Indole production. 18 Multiple Test Media
  • 20. 20 Positive outcome: Our starch agar experiment results showed that our organism can hydrolyse the starch. Upon addition of iodine on the agar, clearing occured as whitish color around the colonies which is an indicator of both alpha and beta amylase activity. It has been previously shown that Bacillus subtilis gives positive reaction clearing colony around [1,2]. Therefore, this outcome supports that our unknown bacterium might be Bacillus subtilis. Negative outcome Our starch agar experiment results showed that our organism cannot hydrolyse the starch. Upon addition of iodine on the agar, nothing changed around the colonies which is an indicator of no amylase activity. It has been previously shown that Escherichia coli gives negative reaction on starch agar test [3]. Therefore, this outcome supports that our unknown bacterium might be Escherichia coli. In-text reference In-text reference
  • 21. 21 • 4 pages (maximum) of reports will be arranged as follows: • Cover page: Your section and group number. Write your group members as well. • Maximum 2 pages of discussion (1 page is preferred). • 1 separate page for the reference list. (Check for the reference tools for correct reference formatting). • Font: Arial---10 puncta---Centered text---Word format • Mail your reports to: guloglu.sercann@gmail.com • No questions about any test’s evaluation will be answered !!! • You can use websites as a reference. However, scientific article references will receive extra points. • You have 7 days for report submission. • Earlier report submissions will get you extra 5 points per day up to 4 days (+20 points in total) • Later report submissions will take away your 10 points per day.
  • 22. 22 • Grading of the reports: Points Cover page 5 Introduction pragraph (2-3 sentences) 5.4 Evaluation of 11 different tests (11 separate paragraphs) 5.4 (each paragraph) 59 (total) Conclusion paragraph 5.4 References (correct formatting & correct information) 10 Language & text formatting 5 Correct prediction of the culture 10 Total 100 Scientific article reference +2 (per article) Earlier report submission +5 (per day) +20 (maximum) Later report submission -10 (per day)