b subtilis atcc 23857 (ATCC)
96
Structured Review
ATCC
b subtilis atcc 23857
B Subtilis Atcc 23857, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 360 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/b+subtilis+atcc+23857/Bacillus+subtilis/pm41778798-211-5-7
Average 96 stars, based on 360 article reviews
B Subtilis Atcc 23857, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 360 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/b+subtilis+atcc+23857/Bacillus+subtilis/pm41778798-211-5-7
Average 96 stars, based on 360 article reviews
b subtilis atcc 23857 - by Bioz Stars,
2026-09
96/100 stars
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Cell Culture:Article Title: Genomic and chemical analyses of 713 marine biofilm-derived bacterial strains. Article Snippet: .. S. aureus ATCC 12600 and other:Article Title: Rational two-round modification for developing isopeptide bond-containing antimicrobial peptide with enhanced stability and potent activity against multidrug-resistant gram-negative bacteria. Article Snippet: The peptide CPF-7, developed by our group previously, is a modified analog of the natural antimicrobial peptide CPF-C1, which demonstrated increased antibacterial activity.. However, its perfect α-helical structure contributes to high hemolysis, thereby limiting its applications.. Herein, to improve the druggability of CPF-7, we first introduced isopeptide bonds to modulate helicity, generating analogs with a favorable therapeutic index. Diffusion-based Assay:Article Title: Genomic and chemical analyses of 713 marine biofilm-derived bacterial strains. Article Snippet: .. Disk diffusion assays demonstrated that alteramide A effectively inhibited the growth of S. aureus ATCC 12600 and Clone Assay:Article Title: Microbial production of propionic acid through a novel β-alanine route. Article Snippet: Propionic acid is a key three carbon platform chemical with broad applications in food preservation, pharmaceuticals, and polymer production.. Traditional microbial production of propionic acid employing Propionibacterium species is constrained by slow growth, and limited genetic engineering tools, thereby restricting its industrial use.. Here, we report the development of a novel biosynthetic pathway for propionic acid production via the β-alanine route. Construct:Article Title: Microbial production of propionic acid through a novel β-alanine route. Article Snippet: Propionic acid is a key three carbon platform chemical with broad applications in food preservation, pharmaceuticals, and polymer production.. Traditional microbial production of propionic acid employing Propionibacterium species is constrained by slow growth, and limited genetic engineering tools, thereby restricting its industrial use.. Here, we report the development of a novel biosynthetic pathway for propionic acid production via the β-alanine route. Plasmid Preparation:Article Title: Microbial production of propionic acid through a novel β-alanine route. Article Snippet: Propionic acid is a key three carbon platform chemical with broad applications in food preservation, pharmaceuticals, and polymer production.. Traditional microbial production of propionic acid employing Propionibacterium species is constrained by slow growth, and limited genetic engineering tools, thereby restricting its industrial use.. Here, we report the development of a novel biosynthetic pathway for propionic acid production via the β-alanine route. Bacteria:Article Title: High therapeutic index α-helical antimicrobial peptides with repetitive subunit structures against multidrug-resistant bacteria. Article Snippet: De novo design of antimicrobial peptides (AMPs) offers a promising strategy to overcome the limitations of natural AMPs through rational design, providing potential solutions to address the growing risk of traditional antibiotic resistance.. In this study, a series of new AMPs are generated using the α-helical template (XXFY)n and its β-sheet counterpart (KFKY)n (X = Lys, Dab, Orn, or Arg; F = Phe; Y = Leu, Ile, Phe, or Trp; K = Lys; n = 2, 3, 4, or 5), enabling a systematic investigation of their structure-activity relationships (SAR).. The optimal peptide 27, designated as (OOFI)4 (O = Orn, I = Ile), demonstrates potent broad-spectrum antimicrobial activity against both standard and multidrug-resistant bacterial strains, along with low hemolytic toxicity. |