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Shelley returned with plates containing three roasted shrimp each.
Plates containing 30 300 CFU were counted.
We seeded 1 × 105 JAR cells/well in 6-well plates containing coverslips overnight.
The plates containing nutrient agar media were prepared by swabbing them with the microbial cultures.
Transformants were selected on LB plates containing 50 μg/mL gentamycin.
Transformants were screened in the YPDS plates containing 100 μg ml−1 of zeocin.
The plates containing the disks were incubated overnight at 37 °C.
Diluted extract was plated on peptone sucrose agar plates containing 15 mg/L cephalexin.
Plates containing only the agar media with no wood added acted as controls.
Transformants were screened for laccase production on buffered minimal methanol agar plates containing ABTS.
Transformants were selected on GAM plates containing 1% d-glucose and 5 μg/mL of erythromycin.
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