“…Then, 50 μL of diluted bacterial solution (10 −6 ) was added to the inclusion complex solution and incubated at 37 °C, and the absorbance value measured at 600 nm at 0, 2, 4, 6, 8, 10, 12, 24, 30, 36 and 48 h, respectively. Meanwhile, at 12 h, the appropriate amounts of bacterial solution were taken out and diluted 10 7 times, and then 50 μL of diluted bacterial solution was added to a mannitol salt agar plate, and the plates were cultured at 37 °C for 48 h. 27 All samples were characterized in triplicate.…”