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This is also the first research on the screening of a bacterium with the NH4 +-N-degrading ability from the tailings of REE mines.
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In a screening of soil bacteria, the strain E. coli AC-521 was isolated based on its ability to use glycerol as carbon source and to grow quickly under aerobic conditions.
For screening of lipase producing bacteria, the bacteria pure cultures on the LB plates were streaked on selective plate media, which is Rhodamine B (28 g nutrient agar, 4 g sodium chloride, 10 mg rhodamine B, 10 mL olive oil in 1 L distilled water with pH 7 adjusted by the addition of sodium hydroxide prior autoclaved).
Initial screening of bacteria from a subset of the 77 sampled planthoppers yielded high quality 16S rDNA sequences.
The objective of this study was to estimate the biosynthetic potential of X. albilineans and X. oryzae by in silico analyses of their uncharacterized NRPS gene clusters and to identify other bacterial candidates for extended genome mining by PCR screening of a collection of 94 plant pathogenic bacteria for the presence of the XaPPTase gene and other NRPS-associated genes.
PCR screening of a collection of 94 plant pathogenic bacteria indicates that these novel NRPS gene clusters are specific to the genus Xanthomonas and are also present in Xanthomonas translucens and X. oryzae pv.
In the present study, we report a novel strain SK.DU.4, identified during screening of soil bacteria for antimicrobial substances production, which produces both bacteriocin-like peptide and lipopeptide.
Rapid screening of pathogenic bacteria contaminated foods is the key to prevent and control the outbreaks of foodborne illness.
The method can also be used to fabricate antimicrobial coatings and surfaces for inactivation and screening of viable bacteria.
The results obtained in this study using the phenotypic method of screening of cultured bacteria are consistent with what has been reported in the literature.
Here we describe the isolation and screening of keratinolytic bacteria that effectively decompose chicken feathers, as well as optimization of culture conditions for one bacterial isolate to maximize accumulation of proteins and amino acids and characterization of the resultant hydrolysate.
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