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However, bacterial sinusitis such as those with Staphylococcus aureus biofilm infection point to more recalcitrant CRS subtypes, focusing research efforts into topical antimicrobial therapies.
If as with methicillin resistance Staphylococcus aureus (MRSA) vancomycin creep occurs (rising MIC values), newer antimicrobial agents will be needed.
K. oxytoca is a microorganism which can be associated with clinical infectious crystalline keratopathy, presenting as a mixed infection along with Staphylococcus species.
The CauloGA gene product that was expressed in E. coli was prone to forming inclusion bodies; however, most of the gene product was expressed in a soluble and active form when it was expressed as a fusion protein with Staphylococcus Protein A. The fusion protein was purified using an IgG Sepharose column and was identified as the active GA.
In the present work, we cloned the cc2282 gene of C. crescentus, and identified it as the CauloGA gene based on the properties of the gene product that was expressed in E. coli as a protein fused with Staphylococcus Protein A at the N-terminus.
As was the case with Staphylococcus aureus these OMPs differed considerably with the MH agar and MH broth grown bacteria.
With Staphylococcus aureus as the causative microorganism, the mortality rate may further increase to 54 % [ 16].
Coagulase-negative staphylococci, with Staphylococcus epidermidis as the most frequently isolated species, have become the leading cause of hospital-acquired infections and infections of indwelling medical devices.
A PCR-positive valve sample taken from a patient with Staphylococcus aureus endocarditis was used as a positive control.
Wound colonization with Staphylococcus spp. and S. aureus were considered as dependent variables.
Similarly, 16S rRNA sequence of DAB-IW showed similarity with Staphylococcus sp. by BLAST analysis and it was named as Staphylococcus sp. DAB-1W.
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