Some bacteria are able to produce an enzyme called urease t - PowerPoint Presentation

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Some bacteria are able to produce an enzyme called urease that attacks the nitrogen and carbon bond in amide compounds such as urea, forming the end products ammonia, CO2, and water.

Urease test is used screen lactose negative

gram-negative Enterobacteriaceae

on differential media plated with materials from stool specimen, helping to differentiate Salmonella and Shigella species which are urease negative from the urease positive non-pathogen. Proteus, and some Citrobacter species and some Haemophilus species are urease positive

. P

. mirabilis is a major cause of human urinary tract infections.

Ureas

TestSlide3

Urease-Producing by some Enterobacteriaceae

like:

Proteus

Klebsiella pneumoniae Enterobacter

cloacae

Yersinia enterocoliticaSlide4

To differentiate between urease positive and urease negative bacteria using Christensen urea agar, that contains

Urea (20.00 g/l),

Gelatin Peptone (1.00 g/l), Sodium Chloride (5.00

g/l), Dextrose (1.00 g/l), Phenol Red (0.012

g/l) and Monopotassium Phosphate (2.00

g/l). Some bacteria can utilize urea as a non-carbohydrate carbon source using urease enzyme.

PrincipleSlide5

Dextrose are presents in a small amount in media, so bacteria have to find another carbon source or it will stop growing.

Urease activity (the urease test) is detected by growing bacteria in medium containing urea and using a pH indicator such as phenol red. When urea is hydrolyzed, ammonia accumulates in the medium and makes it alkaline. This increase in pH causes the indicator to change from orange-red to deep pink or purplish red and is a positive test for urea hydrolysis.Slide6

Streak the slant of Christensen`s urea

medium with

the test organism.Incubate at 35

oC (or the appropriate temperature for the organism) for 24 hours to four days.

Some bacteria have a delayed urease reaction that

may require an incubation period longer than 48 hours.

Positive: A bright pink colour develops on the slant and may extends throughout the medium

Negative: No change in the original colour of the medium.

ProcedureSlide7
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The ability to degrade amino acids to identifiable end products is often used to differentiate among bacteria. Tryptophan, for example, is hydrolyzed to

Indole,

pyruvic acid and ammonia by

tryptophanase.

The pyruvic acid can be further metabolized to produce large amounts of energy. The ammonia is available for use in synthesis of new amino acids.

Indole can be detected by reaction with

Kovac's

reagent (para-

dimethylaminobenzaldehyde

in alcohol) to produce a red color.

Indole TestSlide9

Inoculate Tryptone broth or

SIM media

{contains tryptophan} with inoculating loop.

Incubate at 37°C for 24 hours .After incubation interval, add 1 ml Kovacs reagent, shake the tube gently and read immediately.

ProcedureSlide10

Result

A red color in the top layer indicates the presence of

indole

The absence of color means that indole was not produced.

Used in the differentiation of genera and species. e.g.

E. coli (+) from Klebsiella,

Enterobacter

aerogenes

(-).Slide11
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Nitrate

reductase

test : is a test to differentiate between bacteria based on their ability or inability to reduce nitrate (NO

3−) to nitrite (NO2−) using anaerobic respiration.

Some of these bacteria possess the enzymes to further reduce the nitrite to either the ammonium ion or molecular nitrogen.

Nitrate Reduction TestSlide13

Organisms that possess the enzyme, nitrate

reductase

reduces nitrate to nitrite.

The nitrite ions are detected by the addition of Sulfanilic acid and N,N-dimethyl-1-naphthylamine to the culture. Any nitrite in the medium will react with these reagents to produce a pink or red color.

PrincipleSlide14

To determine if nitrates were reduced past

nitrite:

a small amount of zinc powder is added to the culture containing the reagents. Since zinc reduces nitrates to nitrites, a pink or red color will appear and verifies the fact that nitrates were not reduced to nitrites by the bacteria (nitrate unreacted). If a red color does not appear, the nitrates in the medium were reduced past the nitrite stage to either

ammonium

or nitrogen gas (nitrate reacted).

If a culture does not produce a color

change, several

possibilities exist:

the bacteria possess nitrate

reductase

and also reduce nitrite further to

ammonium

or molecular nitrogen

;

they possess other enzymes that reduce nitrite to

ammonium;

nitrates were not reduced by the bacteria. Slide15

Inoculate a nitrate

broth (0.5% potassium nitrate (KNO3

)) with the test organism.

Incubate at 37C for 24 hr.Add 5 drops of reagent A (

Sulfanic acid) and 5 drops of reagent B (

naphthylamine ) to the broth.

If

nitrate is present in the medium, it will turn red within 1 to

2 minutes

; if it is absent, there will be no color change.

Positive:

A red color.

Negative

:

Colorless

.

Negative tests should be confirmed by adding several grains of zinc powder and gently shaking the

tube.

Positive

:

Colorless

Negative:

Red

color

ProcedureSlide16

Result

Reaction

N2 Gas

Color After

Adding Reagents

Color After Adding Zinc

NO3 To NO2

 None

Red

(Not Added)

NO3 To N2

Yes

No Color

No Color

NO3 To Ammonia

 None

No Color

No Color

NO3-No Reaction

 None

No Color

Pink-red Slide17
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Three different bacteria that give three different nitrate reduction results will be learned.

Staphylococcus epidermidis

is unable to use nitrate as a terminal electron acceptor; therefore, it cannot reduce nitrate.

Escherichia coli

can reduce nitrate only to nitrite.

Pseudomonas

fluorescens

are characterized by excretion of diffusible yellow-green pigments that fluoresce in ultraviolet light) often reduces nitrate completely to molecular nitrogen.

Significance of Nitrate Reduction TestSlide22

Safety consideration

Since N, N-dimethyl-1-naphthylamine might be carcinogenic (nitrite test reagent B), wear disposable gloves and avoid skin contact or aerosols.

The acids in nitrite test reagent A are caustic.

Avoid skin contact and do not breathe the vapors.

Be careful when working with zinc. Do not inhale or allow contact with skin.

No mouth pipetting. Slide23