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For instance, methanol extract showed a good antibacterial result against S. aureus, E. coli and S. typhi with minimum zone of inhibition 13.5 + 0.40, 13.9 + 0.16 and 10.1 + 0.04 respectively however, the highest minimum inhibition zone was recorded in ethyl acetate extract against S. pyogens and K. pneumoniae with minimum zone of inhibition 17.1 + 0.14 and 16.8 + 0.41 respectively.
The phloretin standard, with a concentration of 5.00 mg/ml, had a maximum inhibition zone against S. aureus and E. coli, whereas the EAE, with a concentration of 5.00 mg GAE/ml, had the minimum inhibition zone against both S. aureus and E. coli.
However, the compounds were less active than the reference drug (Gentamycine), which showed minimum inhibition zone of 21 mm (Pseudomonas aeruginosa) and maximum of 28 mm (Escherichia coli) inhibition zone.
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Effective number of isolates and minimum-maximum inhibition zone values of 158 isolates from 9 different species tested in vitro for antifungal properties of the chitinase enzyme partially purified from Bacillus subtilis TV-125A extracellularly in a petri medium against pathogenic fungi are given in Table 1.
The minimum inhibitory concentration (MIC), minimum bactericidal (MBC), minimum fungicidal concentration (MFC) [ 22] and the inhibition zone of the OC against the test microorganisms were determined by the broth microdilution method.
The antibacterial assays in this study were performed by using inhibition zone diameters, MIC (Minimum inhibitory concentration) and MBC (Minimal bactericidal concentration) methods.
The obtained data, expressed as diameter of the inhibition zone (DIZ) and minimum inhibition concentration (MIC) for the test compounds 5a-k and for the reference drug, fluconazole, are presented in Table 1.
Minimum inhibition concentration for inhibiting 50% of the pathogen.
Every model closely approximates the branch distribution as a function of metamer position, the total branch number, the apical inhibition zone size and the minimum distance of a branch to its closest neighbour for every corresponding mutant.
(Z – AB ) 5 μM BUM treatment did not affect the branch number in WT (Z ), the apical inhibition zone size (AA ) and the minimum distance between lateral branches (AB ) (mean ± SD).
(P – R ) 5 μM NPA treatment did not affect the branch number in GH3::GUS transgenics (P ), the apical inhibition zone size (Q ) and the minimum distance between lateral branches (R ).
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