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Table 2 In vitro antibacterial activity of purified phospholipase A2 enzymes from snake venoms.

From: In vitro antimicrobial activity of natural toxins and animal venoms tested against Burkholderia pseudomallei

Phospholipase A2

enzymes (PLA2s)

Snake species (Scientific name)

Mol. wt.(kDa)

Conc. (mg/mL)

Micro-organisms

    

B. pseudomallei (Strain KHW)

B. pseudomallei (Strain TES)

Crotoxin A (CA)

Crotalus durissus terrificus

23.5

0.5 mg/mL

-

-

Crotoxin B (CB)

Crotalus durissus terrificus

23.5

0.5 mg/mL

24.8 ± 0.089

27.6 ± 0.133

Ammodytoxin A

Vipera ammodytes ammodytes

13.8

0.5 mg/mL

-

-

Mojave toxin

Crotalus scutulatus scutulatus

23.5

0.5 mg/mL

-

-

β-Bungarotoxin

Bungarus multicinctus

20.5

0.5 mg/mL

-

-

Taipoxin

Oxyuranus scutellatus scutellatus

45.6

0.5 mg/mL

-

 

Mulgatoxin

Pseudechis australis

13.2

0.5 mg/mL

20.5 ± 0.075

22.7 ± 0.117

Daboiatoxin (DbTx)

Daboia russelli siamensis

15.0

0.5 mg/mL

24.8 ± 0.103

26.2 ± 0.121

Bee venom PLA2

Apis mellifera

19.0

0.5 μg/mL

18.3 ± 0.089

20.4 ± 0.075

  1. *The values given represent a venom inhibition zone in mm, including the 7 mm diameter of the disc, after 24 h incubation. The bacterial inoculum per plate contained 3.2 × 108 cfu/mL forming units which were spread onto the TS agar surface with sterile cotton swap. Sterile paper discs (7 mm diameter) were placed onto the TS agar surface and 20 μL of enzymes (0.5 mg/ml concentration) added, Control (0); No activity (-).