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Lysine Decarboxylase Broth (LDB) | Enterobacteriaceae Detection – Ausamics

Lysine Decarboxylase Broth (LDB) | Enterobacteriaceae Detection – Ausamics

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AuSaMicS Life Science • Biochemical Identification Media

Lysine Decarboxylase Broth

Differential Broth for Lysine Decarboxylase Activity

Standard liquid medium for determining whether a microorganism possesses lysine decarboxylase, enabling conversion of L-lysine to cadaverine under anaerobic conditions. Widely used in Salmonella confirmation, Enterobacteriaceae differentiation, and conventional biochemical identification workflows.

AS-1278 🧪 Biochemical Identification ✓ Salmonella Workflow 🔬 Decarboxylase Test
Readout: Yellow to purple reversal Requirement: Mineral oil overlay Use: Enterobacteriaceae differentiation

Biochemical Media Specialist

Salmonella Confirmation - Classical lysine-positive screening support
Viability Control - Initial glucose fermentation step
Clear Indicator System - Bromocresol purple colour shift
Anaerobic Reaction Design - Mineral oil overlay method
Routine Lab Utility - Conventional identification series
Classical Decarboxylase Test
Essential for enteric identification workflows

🧪 Complete Formulation & Reaction Principle

📋 Composition (per Liter)

Ingredient Concentration Primary Function Contribution
L-Lysine HCl 5.0 g Target substrate Provides lysine for decarboxylase reaction
Yeast Extract 3.0 g Growth support Provides nitrogen, vitamins, and growth factors
Glucose 1.0 g Fermentable carbohydrate Initial acidification confirms viability
Bromocresol Purple 0.02 g pH indicator Yellow in acid, purple in alkaline reaction
Final pH: 6.8 ± 0.2 at 25°C

⚗️ Principle of the Test

Viability Check
Small amount of glucose is fermented first, turning the broth yellow
Anaerobic Decarboxylation
Mineral oil overlay creates conditions required for lysine decarboxylase activity
Alkaline Reversal
Positive organisms convert lysine to cadaverine, returning the broth to purple
Why Lysine Decarboxylase Broth? It helps distinguish key enteric pathogens and coliforms in classical biochemical identification, especially in Salmonella workups.

Complete Enteric Identification Media Portfolio

Medium Type Main Readout Best Application Workflow Position Key Advantage
Lysine Decarboxylase Broth Biochemical differential broth Yellow to purple reversal Salmonella confirmation and enteric differentiation After primary isolation / screening Classical lysine decarboxylase determination
Triple Sugar Iron Agar Differential tube medium Sugar use, gas, H2S Primary enteric screening Early screening step Multiple reactions in one tube
Kligler Iron Agar Differential tube medium Glucose/lactose fermentation and H2S Preliminary enteric differentiation Initial workup Classic enteric separation tool
Urea Broth / Urea Agar Biochemical reaction medium Urease activity Differentiation of urease-positive enterics Supplementary test Rapid enzyme-based interpretation
Citrate Agar Utilization medium Alkaline citrate utilization IMViC and enteric ID Supplementary biochemical step Common companion test in enteric profiles

Strategic Medium Selection for Lysine Decarboxylase Testing

✅ Lysine Decarboxylase Broth Advantages

  • Classical Salmonella Support: Useful in standard confirmation workflows
  • Built-in Viability Check: Initial glucose acidification confirms growth
  • Clear Colour Logic: Purple reversal indicates positive decarboxylation
  • Widely Recognised: Used in conventional and regulatory identification series
  • Good Differential Utility: Helps separate Salmonella/Citrobacter from many other enterics

⚠️ Method Considerations

  • Anaerobic Condition Required: Mineral oil or paraffin overlay is essential
  • Heat Sensitivity: Over-sterilization can affect lysine performance
  • Interpretation Timing Matters: Early and late reads can differ
  • Variable Organisms Exist: Some Proteus / Providencia reactions may be atypical or fading

🎯 Best-Fit Applications

  • Salmonella Confirmation: Follow-up after TSI/KIA screening
  • Citrobacter Differentiation: Support in separating coliform groups
  • API / Conventional ID Workflows: Enteric biochemical profiling
  • Reference Laboratory Testing: Regulatory and classical microbiology methods

📊 Interpretation Guide

Observation Interpretation Typical Meaning Examples
Initial yellow, then purple Lysine decarboxylase positive Viability confirmed, decarboxylation occurred Salmonella, many Citrobacter
Remains yellow Lysine decarboxylase negative Glucose fermentation without alkaline reversal E. coli, Shigella, Klebsiella, Enterobacter
Fading / colourless / variable Variable or atypical Interpret with caution and companion tests Proteus, some Providencia

🔬 Quality Control & Performance Guidance

Typical Positives:
Salmonella (non-typhi), many Citrobacter
some Providencia
Typical Negatives:
E. coli, Shigella, Klebsiella
Enterobacter, Serratia
Incubation:
35–37°C
18–48 h after overlay
Preparation Note:
Sterilize only 10–12 min
Lysine is heat-sensitive
Positioning: A core biochemical broth for laboratory identification of enteric bacteria, especially useful in Salmonella confirmation and classical regulatory microbiology workflows.

📋 Technical Specifications

Catalogue Number AS-1278
Medium Type Differential biochemical broth
Base Weight 9.02 g/L
Final pH 6.8 ± 0.2 (at 25°C)
Indicator Bromocresol Purple
Anaerobic Requirement Mineral oil or liquid paraffin overlay
Dispensing Volume 4–5 mL per tube
Sterilization 121°C for only 10–12 minutes
Incubation 35–37°C for 18–48 h
Prepared Tube Storage 2–8°C, protected from light, up to 3 months

🧫 Primary Applications

  • ✓ Confirmation of Salmonella after TSI/KIA screening
  • ✓ Differentiation of Citrobacter from other coliforms
  • ✓ Conventional biochemical identification series
  • ✓ Support for API-style and regulatory workflows

⚗️ Preparation & Test Procedure

  1. 1. Dissolve 9.02 g dehydrated medium in 1 L purified water.
  2. 2. Dispense 4–5 mL into small tubes.
  3. 3. Autoclave at 121°C for only 10–12 minutes.
  4. 4. Inoculate heavily from an 18–24 h pure culture.
  5. 5. Overlay with 8–10 mm sterile mineral oil or liquid paraffin and incubate at 35–37°C for 18–48 h.

📦 Storage & Intended Use

Prepared tubes: Store at 2–8°C, protected from light.

Use period: Use within 3 months for optimal performance.

Test note: Read results in the context of proper overlay and incubation timing.

Notice: For laboratory identification use only.

AuSaMicS Life Science: Professional microbiology media for biochemical identification, food safety, clinical and industrial microbiology, research, and routine laboratory workflows. Product information is provided for laboratory and technical evaluation purposes only.

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