standard bacterial reference strains atcc 25922 Search Results


99
ATCC e coli strain atcc 25922
Case Summary of 15 Patients from Whom ESBL-producing Bacteria were Isolated from Sputum.
E Coli Strain Atcc 25922, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
ATCC escherichia coli
( a ) E. coli (ATCC 25922); ( b ) clinical isolate of imipenem-resistant E. coli with (red curves) and without (black curves) imipenem treatment; ( c ) signal ratio of 654-cm −1 SERS peak ( r 654 ) of E. coli (ATCC 25922) as a function of imipenem treatment time; ( d ) r 654 of imipenem-resistant E. coli as a function of imipenem treatment time; ( e ) signal ratio of 724-cm −1 SERS peak ( r 724 ) of E. coli (ATCC 25922) as a function of imipenem treatment time; ( f ) r 724 of imipenem-resistant E. coli as a function of imipenem treatment time. Black and red curves represent the mean SERS spectra, while gray and light red curves represent their corresponding standard deviation.
Escherichia Coli, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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95
ATCC bacterial strains
( a ) E. coli (ATCC 25922); ( b ) clinical isolate of imipenem-resistant E. coli with (red curves) and without (black curves) imipenem treatment; ( c ) signal ratio of 654-cm −1 SERS peak ( r 654 ) of E. coli (ATCC 25922) as a function of imipenem treatment time; ( d ) r 654 of imipenem-resistant E. coli as a function of imipenem treatment time; ( e ) signal ratio of 724-cm −1 SERS peak ( r 724 ) of E. coli (ATCC 25922) as a function of imipenem treatment time; ( f ) r 724 of imipenem-resistant E. coli as a function of imipenem treatment time. Black and red curves represent the mean SERS spectra, while gray and light red curves represent their corresponding standard deviation.
Bacterial Strains, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
ATCC standard gram negative strain
Scanning Electron Microscopy (SEM) images showing the morphological effects of silver nanoparticles synthesized from C. arvensis. ( A – C ) demonstrate the effect on Gram-positive S. aureus (MRSA and ST), E-H demonstrate the effect <t>on</t> <t>Gram-negative</t> E. coli ESBL and ST) bacterial strains. described above, and the cells exhibited a division-related septum, broadening, and cytoplasm leakage. Scanning electron microscope images showed that the untreated control groups ( A , C , E , G ), bacterial cells exhibited normal morphology with intact cell walls and smooth surfaces. In contrast, treated cells ( B , D , F , H ) showed significant morphological changes: S. aureus cells displayed shrinkage and deformations in their spherical shape, while E. coli cells exhibited marked structural disintegration and severe membrane damage. These observations confirm the destructive effects of silver nanoparticles on bacterial cell integrity. Most of the cells were damaged and perforated, which changed the cell structure and shape, and it was noted that some of them were empty. In addition, most cells appeared to stick together compared to untreated cells. As is clear in .
Standard Gram Negative Strain, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
ATCC bacterial strains escherichia coli atcc 25922
Scanning Electron Microscopy (SEM) images showing the morphological effects of silver nanoparticles synthesized from C. arvensis. ( A – C ) demonstrate the effect on Gram-positive S. aureus (MRSA and ST), E-H demonstrate the effect <t>on</t> <t>Gram-negative</t> E. coli ESBL and ST) bacterial strains. described above, and the cells exhibited a division-related septum, broadening, and cytoplasm leakage. Scanning electron microscope images showed that the untreated control groups ( A , C , E , G ), bacterial cells exhibited normal morphology with intact cell walls and smooth surfaces. In contrast, treated cells ( B , D , F , H ) showed significant morphological changes: S. aureus cells displayed shrinkage and deformations in their spherical shape, while E. coli cells exhibited marked structural disintegration and severe membrane damage. These observations confirm the destructive effects of silver nanoparticles on bacterial cell integrity. Most of the cells were damaged and perforated, which changed the cell structure and shape, and it was noted that some of them were empty. In addition, most cells appeared to stick together compared to untreated cells. As is clear in .
Bacterial Strains Escherichia Coli Atcc 25922, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
ATCC p aeruginosa atcc 27853 bacterial strains
Scanning Electron Microscopy (SEM) images showing the morphological effects of silver nanoparticles synthesized from C. arvensis. ( A – C ) demonstrate the effect on Gram-positive S. aureus (MRSA and ST), E-H demonstrate the effect <t>on</t> <t>Gram-negative</t> E. coli ESBL and ST) bacterial strains. described above, and the cells exhibited a division-related septum, broadening, and cytoplasm leakage. Scanning electron microscope images showed that the untreated control groups ( A , C , E , G ), bacterial cells exhibited normal morphology with intact cell walls and smooth surfaces. In contrast, treated cells ( B , D , F , H ) showed significant morphological changes: S. aureus cells displayed shrinkage and deformations in their spherical shape, while E. coli cells exhibited marked structural disintegration and severe membrane damage. These observations confirm the destructive effects of silver nanoparticles on bacterial cell integrity. Most of the cells were damaged and perforated, which changed the cell structure and shape, and it was noted that some of them were empty. In addition, most cells appeared to stick together compared to untreated cells. As is clear in .
P Aeruginosa Atcc 27853 Bacterial Strains, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
DSMZ water solvents against standard bacteria
Scanning Electron Microscopy (SEM) images showing the morphological effects of silver nanoparticles synthesized from C. arvensis. ( A – C ) demonstrate the effect on Gram-positive S. aureus (MRSA and ST), E-H demonstrate the effect <t>on</t> <t>Gram-negative</t> E. coli ESBL and ST) bacterial strains. described above, and the cells exhibited a division-related septum, broadening, and cytoplasm leakage. Scanning electron microscope images showed that the untreated control groups ( A , C , E , G ), bacterial cells exhibited normal morphology with intact cell walls and smooth surfaces. In contrast, treated cells ( B , D , F , H ) showed significant morphological changes: S. aureus cells displayed shrinkage and deformations in their spherical shape, while E. coli cells exhibited marked structural disintegration and severe membrane damage. These observations confirm the destructive effects of silver nanoparticles on bacterial cell integrity. Most of the cells were damaged and perforated, which changed the cell structure and shape, and it was noted that some of them were empty. In addition, most cells appeared to stick together compared to untreated cells. As is clear in .
Water Solvents Against Standard Bacteria, supplied by DSMZ, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
ATCC pathogen reference strains
Scanning Electron Microscopy (SEM) images showing the morphological effects of silver nanoparticles synthesized from C. arvensis. ( A – C ) demonstrate the effect on Gram-positive S. aureus (MRSA and ST), E-H demonstrate the effect <t>on</t> <t>Gram-negative</t> E. coli ESBL and ST) bacterial strains. described above, and the cells exhibited a division-related septum, broadening, and cytoplasm leakage. Scanning electron microscope images showed that the untreated control groups ( A , C , E , G ), bacterial cells exhibited normal morphology with intact cell walls and smooth surfaces. In contrast, treated cells ( B , D , F , H ) showed significant morphological changes: S. aureus cells displayed shrinkage and deformations in their spherical shape, while E. coli cells exhibited marked structural disintegration and severe membrane damage. These observations confirm the destructive effects of silver nanoparticles on bacterial cell integrity. Most of the cells were damaged and perforated, which changed the cell structure and shape, and it was noted that some of them were empty. In addition, most cells appeared to stick together compared to untreated cells. As is clear in .
Pathogen Reference Strains, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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98
ATCC gram negative standard strains
Scanning Electron Microscopy (SEM) images showing the morphological effects of silver nanoparticles synthesized from C. arvensis. ( A – C ) demonstrate the effect on Gram-positive S. aureus (MRSA and ST), E-H demonstrate the effect <t>on</t> <t>Gram-negative</t> E. coli ESBL and ST) bacterial strains. described above, and the cells exhibited a division-related septum, broadening, and cytoplasm leakage. Scanning electron microscope images showed that the untreated control groups ( A , C , E , G ), bacterial cells exhibited normal morphology with intact cell walls and smooth surfaces. In contrast, treated cells ( B , D , F , H ) showed significant morphological changes: S. aureus cells displayed shrinkage and deformations in their spherical shape, while E. coli cells exhibited marked structural disintegration and severe membrane damage. These observations confirm the destructive effects of silver nanoparticles on bacterial cell integrity. Most of the cells were damaged and perforated, which changed the cell structure and shape, and it was noted that some of them were empty. In addition, most cells appeared to stick together compared to untreated cells. As is clear in .
Gram Negative Standard Strains, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
ATCC pantothenamides against other strains
Structure of pantothenic acid and N-substituted <t>pantothenamides</t>
Pantothenamides Against Other Strains, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Case Summary of 15 Patients from Whom ESBL-producing Bacteria were Isolated from Sputum.

Journal: Internal Medicine

Article Title: Isolation of ESBL-producing Bacteria from Sputum in Community-acquired Pneumonia or Healthcare-associated Pneumonia Does Not Indicate the Need for Antibiotics with Activity against This Class

doi: 10.2169/internalmedicine.8867-17

Figure Lengend Snippet: Case Summary of 15 Patients from Whom ESBL-producing Bacteria were Isolated from Sputum.

Article Snippet: E. coli strain ATCC 25922 and K. pneumoniae strain ATCC 700603 were used as negative and positive controls, respectively, for ESBL production.

Techniques: Bacteria, Isolation

( a ) E. coli (ATCC 25922); ( b ) clinical isolate of imipenem-resistant E. coli with (red curves) and without (black curves) imipenem treatment; ( c ) signal ratio of 654-cm −1 SERS peak ( r 654 ) of E. coli (ATCC 25922) as a function of imipenem treatment time; ( d ) r 654 of imipenem-resistant E. coli as a function of imipenem treatment time; ( e ) signal ratio of 724-cm −1 SERS peak ( r 724 ) of E. coli (ATCC 25922) as a function of imipenem treatment time; ( f ) r 724 of imipenem-resistant E. coli as a function of imipenem treatment time. Black and red curves represent the mean SERS spectra, while gray and light red curves represent their corresponding standard deviation.

Journal: Scientific Reports

Article Title: Rapid bacterial antibiotic susceptibility test based on simple surface-enhanced Raman spectroscopic biomarkers

doi: 10.1038/srep23375

Figure Lengend Snippet: ( a ) E. coli (ATCC 25922); ( b ) clinical isolate of imipenem-resistant E. coli with (red curves) and without (black curves) imipenem treatment; ( c ) signal ratio of 654-cm −1 SERS peak ( r 654 ) of E. coli (ATCC 25922) as a function of imipenem treatment time; ( d ) r 654 of imipenem-resistant E. coli as a function of imipenem treatment time; ( e ) signal ratio of 724-cm −1 SERS peak ( r 724 ) of E. coli (ATCC 25922) as a function of imipenem treatment time; ( f ) r 724 of imipenem-resistant E. coli as a function of imipenem treatment time. Black and red curves represent the mean SERS spectra, while gray and light red curves represent their corresponding standard deviation.

Article Snippet: Methicillin-susceptible Staphylococcus aureus (ATCC 29213) and Escherichia coli (ATCC 25922 and ATCC 35218) were obtained from American Type Culture Collection (ATCC).

Techniques: Standard Deviation

After being treated by antibiotics for 0, 0.5, 1 and 2 hours, the bacteria were stained with PI (fluorescing red) and SYTO 9 (fluorescing green). BF: bright-field image; FL: fluorescence image. ( a ) S. aureus (ATCC 29213) treated with oxacillin; ( b ) E. coli (ATCC 25922) treated with imipenem; ( c ) percentage of dead bacteria ( f dead ): S. aureus (black columns) and E. coli (gray columns). f dead = N r /( N g + N r − N g + r ), where N r is the count of the red signatures, N g is the count of the green signatures, and N g + r is the count that the green and red signatures overlap. The scale bars represent 20 μ m.

Journal: Scientific Reports

Article Title: Rapid bacterial antibiotic susceptibility test based on simple surface-enhanced Raman spectroscopic biomarkers

doi: 10.1038/srep23375

Figure Lengend Snippet: After being treated by antibiotics for 0, 0.5, 1 and 2 hours, the bacteria were stained with PI (fluorescing red) and SYTO 9 (fluorescing green). BF: bright-field image; FL: fluorescence image. ( a ) S. aureus (ATCC 29213) treated with oxacillin; ( b ) E. coli (ATCC 25922) treated with imipenem; ( c ) percentage of dead bacteria ( f dead ): S. aureus (black columns) and E. coli (gray columns). f dead = N r /( N g + N r − N g + r ), where N r is the count of the red signatures, N g is the count of the green signatures, and N g + r is the count that the green and red signatures overlap. The scale bars represent 20 μ m.

Article Snippet: Methicillin-susceptible Staphylococcus aureus (ATCC 29213) and Escherichia coli (ATCC 25922 and ATCC 35218) were obtained from American Type Culture Collection (ATCC).

Techniques: Bacteria, Staining, Fluorescence

( a ) Signal ratio of 730-cm −1 SERS peak ( r 730 ) of S. aureus versus vancomycin treatment time at concentrations of 0.5 μ g/ml (light gray columns), 1 μ g/ml (gray columns), and 2 μ g/ml (black columns); ( b , c ) signal ratios of 654-cm −1 SERS peak ( r 654 ) and 724-cm −1 SERS peak ( r 724 ) of E. coli , respectively, versus imipenem treatment time at concentrations of 0.03 μ g/ml (light gray columns), 0.06 μ g/ml (gray columns), and 0.12 μ g/ml (black columns).

Journal: Scientific Reports

Article Title: Rapid bacterial antibiotic susceptibility test based on simple surface-enhanced Raman spectroscopic biomarkers

doi: 10.1038/srep23375

Figure Lengend Snippet: ( a ) Signal ratio of 730-cm −1 SERS peak ( r 730 ) of S. aureus versus vancomycin treatment time at concentrations of 0.5 μ g/ml (light gray columns), 1 μ g/ml (gray columns), and 2 μ g/ml (black columns); ( b , c ) signal ratios of 654-cm −1 SERS peak ( r 654 ) and 724-cm −1 SERS peak ( r 724 ) of E. coli , respectively, versus imipenem treatment time at concentrations of 0.03 μ g/ml (light gray columns), 0.06 μ g/ml (gray columns), and 0.12 μ g/ml (black columns).

Article Snippet: Methicillin-susceptible Staphylococcus aureus (ATCC 29213) and Escherichia coli (ATCC 25922 and ATCC 35218) were obtained from American Type Culture Collection (ATCC).

Techniques:

( a – c ) Signal ratio of 654-cm −1 SERS peak ( r 654 ) of E. coli of inoculum densities of 10 6 , 10 7 and 10 8 CFU/ml, respectively, after being treated with different concentrations of imipenem for 2 hrs.

Journal: Scientific Reports

Article Title: Rapid bacterial antibiotic susceptibility test based on simple surface-enhanced Raman spectroscopic biomarkers

doi: 10.1038/srep23375

Figure Lengend Snippet: ( a – c ) Signal ratio of 654-cm −1 SERS peak ( r 654 ) of E. coli of inoculum densities of 10 6 , 10 7 and 10 8 CFU/ml, respectively, after being treated with different concentrations of imipenem for 2 hrs.

Article Snippet: Methicillin-susceptible Staphylococcus aureus (ATCC 29213) and Escherichia coli (ATCC 25922 and ATCC 35218) were obtained from American Type Culture Collection (ATCC).

Techniques:

Scanning Electron Microscopy (SEM) images showing the morphological effects of silver nanoparticles synthesized from C. arvensis. ( A – C ) demonstrate the effect on Gram-positive S. aureus (MRSA and ST), E-H demonstrate the effect on Gram-negative E. coli ESBL and ST) bacterial strains. described above, and the cells exhibited a division-related septum, broadening, and cytoplasm leakage. Scanning electron microscope images showed that the untreated control groups ( A , C , E , G ), bacterial cells exhibited normal morphology with intact cell walls and smooth surfaces. In contrast, treated cells ( B , D , F , H ) showed significant morphological changes: S. aureus cells displayed shrinkage and deformations in their spherical shape, while E. coli cells exhibited marked structural disintegration and severe membrane damage. These observations confirm the destructive effects of silver nanoparticles on bacterial cell integrity. Most of the cells were damaged and perforated, which changed the cell structure and shape, and it was noted that some of them were empty. In addition, most cells appeared to stick together compared to untreated cells. As is clear in .

Journal: International Journal of Molecular Sciences

Article Title: Green Synthesis of Silver Nanoparticles with Antibacterial, Anti-Inflammatory, and Antioxidant Activity Using Convolvulus arvensis

doi: 10.3390/ijms27031210

Figure Lengend Snippet: Scanning Electron Microscopy (SEM) images showing the morphological effects of silver nanoparticles synthesized from C. arvensis. ( A – C ) demonstrate the effect on Gram-positive S. aureus (MRSA and ST), E-H demonstrate the effect on Gram-negative E. coli ESBL and ST) bacterial strains. described above, and the cells exhibited a division-related septum, broadening, and cytoplasm leakage. Scanning electron microscope images showed that the untreated control groups ( A , C , E , G ), bacterial cells exhibited normal morphology with intact cell walls and smooth surfaces. In contrast, treated cells ( B , D , F , H ) showed significant morphological changes: S. aureus cells displayed shrinkage and deformations in their spherical shape, while E. coli cells exhibited marked structural disintegration and severe membrane damage. These observations confirm the destructive effects of silver nanoparticles on bacterial cell integrity. Most of the cells were damaged and perforated, which changed the cell structure and shape, and it was noted that some of them were empty. In addition, most cells appeared to stick together compared to untreated cells. As is clear in .

Article Snippet: Four bacterial strains were used in this study: one standard Gram-positive strain ( Staphylococcus aureus ATCC 29213 ), one standard Gram-negative strain ( Escherichia coli ATCC 25922 ), and two clinical isolates (SP1 and SP2) obtained from patient samples.

Techniques: Electron Microscopy, Synthesized, Microscopy, Control, Membrane

Structure of pantothenic acid and N-substituted pantothenamides

Journal:

Article Title: Geminal dialkyl derivatives of N -substituted pantothenamides: Synthesis and antibacterial activity

doi: 10.1016/j.bmc.2011.02.053

Figure Lengend Snippet: Structure of pantothenic acid and N-substituted pantothenamides

Article Snippet: A preliminary screen of these pantothenamides against other strains ( Acinetobacter baumannii ATCC 19606, Klebsiella penumoniae ATCC 13883, Escherichia coli ATCC 25922 and 11775, and Bacillus subtilis ATCC 6051 and 6633) using the agar diffusion method suggests no antimicrobial activity (inhibition zone <1.1 cm for a 1 cm disc impregnated with the desired compound). table ft1 table-wrap mode="anchored" t5 caption a7 MIC (μM) a S. aureus b MRSA c Open in a separate window 9a 7 ± 6 7± 3 Open in a separate window 9b 13 ± 7 13± 2 Open in a separate window 9c 101 ± 45 51 ± 15 Open in a separate window 9d 374 ± 187 374 ± 153 Open in a separate window 9e >715 >715 Open in a separate window 9f 3.2 ± 0.8 3.2 ± 0.9 Open in a separate window 9g >703 >703 Open in a separate window 9h >744 >744 Open in a separate window 9i 376 ± 217 376 ± 109 Open in a separate window 9j 1 ± 0.9 1 ± 0.7 Open in a separate window 9k(N5-pan) 7 ± 2 7 ± 2 Open in a separate window 9l (N9-pan) 0.4 ± 0.2 0.4 ± 0.2 Open in a separate window 9m 24 ± 14 24 ± 14 Open in a separate window a Minimum inhibitory concentrations (MICs) were determined using the following concentrations: 0.5, 1, 2, 4, 8, 16, 32, 64, 128, and 256 μg/mL.

Techniques:

Synthetic route to new N-substituted pantothenamides

Journal:

Article Title: Geminal dialkyl derivatives of N -substituted pantothenamides: Synthesis and antibacterial activity

doi: 10.1016/j.bmc.2011.02.053

Figure Lengend Snippet: Synthetic route to new N-substituted pantothenamides

Article Snippet: A preliminary screen of these pantothenamides against other strains ( Acinetobacter baumannii ATCC 19606, Klebsiella penumoniae ATCC 13883, Escherichia coli ATCC 25922 and 11775, and Bacillus subtilis ATCC 6051 and 6633) using the agar diffusion method suggests no antimicrobial activity (inhibition zone <1.1 cm for a 1 cm disc impregnated with the desired compound). table ft1 table-wrap mode="anchored" t5 caption a7 MIC (μM) a S. aureus b MRSA c Open in a separate window 9a 7 ± 6 7± 3 Open in a separate window 9b 13 ± 7 13± 2 Open in a separate window 9c 101 ± 45 51 ± 15 Open in a separate window 9d 374 ± 187 374 ± 153 Open in a separate window 9e >715 >715 Open in a separate window 9f 3.2 ± 0.8 3.2 ± 0.9 Open in a separate window 9g >703 >703 Open in a separate window 9h >744 >744 Open in a separate window 9i 376 ± 217 376 ± 109 Open in a separate window 9j 1 ± 0.9 1 ± 0.7 Open in a separate window 9k(N5-pan) 7 ± 2 7 ± 2 Open in a separate window 9l (N9-pan) 0.4 ± 0.2 0.4 ± 0.2 Open in a separate window 9m 24 ± 14 24 ± 14 Open in a separate window a Minimum inhibitory concentrations (MICs) were determined using the following concentrations: 0.5, 1, 2, 4, 8, 16, 32, 64, 128, and 256 μg/mL.

Techniques:

Antibacterial activity of N -substituted  pantothenamides  9a–9m

Journal:

Article Title: Geminal dialkyl derivatives of N -substituted pantothenamides: Synthesis and antibacterial activity

doi: 10.1016/j.bmc.2011.02.053

Figure Lengend Snippet: Antibacterial activity of N -substituted pantothenamides 9a–9m

Article Snippet: A preliminary screen of these pantothenamides against other strains ( Acinetobacter baumannii ATCC 19606, Klebsiella penumoniae ATCC 13883, Escherichia coli ATCC 25922 and 11775, and Bacillus subtilis ATCC 6051 and 6633) using the agar diffusion method suggests no antimicrobial activity (inhibition zone <1.1 cm for a 1 cm disc impregnated with the desired compound). table ft1 table-wrap mode="anchored" t5 caption a7 MIC (μM) a S. aureus b MRSA c Open in a separate window 9a 7 ± 6 7± 3 Open in a separate window 9b 13 ± 7 13± 2 Open in a separate window 9c 101 ± 45 51 ± 15 Open in a separate window 9d 374 ± 187 374 ± 153 Open in a separate window 9e >715 >715 Open in a separate window 9f 3.2 ± 0.8 3.2 ± 0.9 Open in a separate window 9g >703 >703 Open in a separate window 9h >744 >744 Open in a separate window 9i 376 ± 217 376 ± 109 Open in a separate window 9j 1 ± 0.9 1 ± 0.7 Open in a separate window 9k(N5-pan) 7 ± 2 7 ± 2 Open in a separate window 9l (N9-pan) 0.4 ± 0.2 0.4 ± 0.2 Open in a separate window 9m 24 ± 14 24 ± 14 Open in a separate window a Minimum inhibitory concentrations (MICs) were determined using the following concentrations: 0.5, 1, 2, 4, 8, 16, 32, 64, 128, and 256 μg/mL.

Techniques: Activity Assay