Exact(1)
The traversal of each data packet increases the pheromone value of each link by ϕ id =ϕ id ∗(1+Δ id ), where Δ id =(E cur (i)) β and β is a constant, generally we set β=0.1.
Similar(59)
{ ( I cur + → T i ( E i, S i, S I i, t i ) ≥ T i - 1 ( E i, S i, S I i, t i ) ) } { ( I cur - → T i ( E i, S i, S I i, t i ) ≤ T i - 1 ( E i, S i, S I i, t i ) ) } Counters the suspicious behavior by limiting the maximum achievable trust value.
Serial dilutions of CUR-I with these antibiotics were mixed in 1 : 1 ratio in MHB.
CUR-I and antibiotics ranged from 1024 to 0.5 μg/mL were used for testing.
The antimicrobial assays were performed with CUR-I in combination with cefaclor, cefodizime, and cefotaxime.
CUR-I, CUR-II, and CUR-III showed single peaks at retention times of 11.13, 13.49, and 14.56 min, respectively.
CUR-I was the major component (<83%) of the crude extract which was used in the present study.
The MIC/MBC values of CUR-I against the test bacterial strains ranged from 125 to 1000 μg/mL.
The in vitro interaction between the CUR-I and antibiotics was quantified by determining the fractional inhibitory concentration (FIC).
The purity of CUR-I, CUR-II, and CUR-III was found to be 98.9%, 98%, and 97.1%, respectively (data not shown).
Antimicrobial susceptibility tests of CUR-I and antibiotics against five diarrhea causing bacteria were performed using the standard broth microdilution method.
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