DC Field | Value | Language |
---|---|---|
dc.contributor.author | H L Han | - |
dc.contributor.author | P T V Pham | - |
dc.contributor.author | Song-Gun Kim | - |
dc.contributor.author | S S Chan | - |
dc.contributor.author | K S Khoo | - |
dc.contributor.author | K W Chew | - |
dc.contributor.author | P L Show | - |
dc.contributor.author | T N T Tran | - |
dc.contributor.author | H T V Nguyen | - |
dc.contributor.author | P T D Nguyen | - |
dc.date.accessioned | 2024-11-15T16:32:56Z | - |
dc.date.available | 2024-11-15T16:32:56Z | - |
dc.date.issued | 2024 | - |
dc.identifier.issn | 1073-6085 | - |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/36312 | - |
dc.description.abstract | Multidrug resistance to pathogens has posed a severe threat to public health. The threat could be addressed by antimicrobial peptides (AMPs) with broad-spectrum suppression. In this study, Brevibacillus halotolerans 7WMA2, isolated from marine sediment, produced AMPs against Gram-positive and Gram-negative bacteria. The AMPs were precipitated by ammonium sulfate 30% (w/v) from culture broth and dialyzed by a 1 kDa membrane. Tryptone Soy Agar (TSA) was used for the cultivation and resulted in the largest bacteria-inhibiting zones under aerobic conditions at 25 °C, 48 h. An SDS-PAGE gel overlay test revealed that strain 7WMA2 could produce AMPs of 5?10 kDa and showed no degradation when held at 121 °C for 30 min at a wide pH 2?12 range. The AMPs did not cause toxicity to HeLa cells with concentrations up to 500 μg/mL while increasing the arbitrary unit up to eight times. The study showed that the AMPs produced were unique, with broad-spectrum antimicrobial ability. | - |
dc.publisher | Springer | - |
dc.title | Isolation and characterization of antimicrobial peptides isolated from Brevibacillus halotolerans 7WMA2 for the activity against multidrug-resistant pathogens | - |
dc.title.alternative | Isolation and characterization of antimicrobial peptides isolated from Brevibacillus halotolerans 7WMA2 for the activity against multidrug-resistant pathogens | - |
dc.type | Article | - |
dc.citation.title | Molecular Biotechnology | - |
dc.citation.number | 12 | - |
dc.citation.endPage | 3627 | - |
dc.citation.startPage | 3618 | - |
dc.citation.volume | 66 | - |
dc.contributor.affiliatedAuthor | Song-Gun Kim | - |
dc.contributor.alternativeName | Han | - |
dc.contributor.alternativeName | Pham | - |
dc.contributor.alternativeName | 김성건 | - |
dc.contributor.alternativeName | Chan | - |
dc.contributor.alternativeName | Khoo | - |
dc.contributor.alternativeName | Chew | - |
dc.contributor.alternativeName | Show | - |
dc.contributor.alternativeName | Tran | - |
dc.contributor.alternativeName | Nguyen | - |
dc.contributor.alternativeName | Nguyen | - |
dc.identifier.bibliographicCitation | Molecular Biotechnology, vol. 66, no. 12, pp. 3618-3627 | - |
dc.identifier.doi | 10.1007/s12033-023-00963-0 | - |
dc.subject.keyword | Broad-spectrum | - |
dc.subject.keyword | Multidrug | - |
dc.subject.keyword | Anti-MRSA | - |
dc.subject.keyword | Non-toxicity | - |
dc.subject.keyword | Thermostable | - |
dc.subject.keyword | pH resistance | - |
dc.subject.local | Broad-spectrum | - |
dc.subject.local | Multidrug | - |
dc.subject.local | Anti-MRSA | - |
dc.subject.local | anti-MRSA | - |
dc.subject.local | Non-toxicity | - |
dc.subject.local | Thermostable | - |
dc.subject.local | pH resistance | - |
dc.description.journalClass | Y | - |
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