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Clorobiocin

  • Review on Plant Antimicrobials: a Mechanistic Viewpoint Bahman Khameneh1, Milad Iranshahy2,3, Vahid Soheili1 and Bibi Sedigheh Fazly Bazzaz3*

    Review on Plant Antimicrobials: a Mechanistic Viewpoint Bahman Khameneh1, Milad Iranshahy2,3, Vahid Soheili1 and Bibi Sedigheh Fazly Bazzaz3*

  • Mechanism of Action of Pefloxacin on Surface Morphology, DNA Gyrase Activity and Dehydrogenase Enzymes of Klebsiella Aerogenes

    Mechanism of Action of Pefloxacin on Surface Morphology, DNA Gyrase Activity and Dehydrogenase Enzymes of Klebsiella Aerogenes

  • Advances in Antimicrobial Resistance Monitoring Using Sensors and Biosensors: a Review

    Advances in Antimicrobial Resistance Monitoring Using Sensors and Biosensors: a Review

  • Challenges of Antibacterial Discovery Lynn L

    Challenges of Antibacterial Discovery Lynn L

  • 539 A2062 516 A83016F 445 Acidic Phospholipids 187

    539 A2062 516 A83016F 445 Acidic Phospholipids 187

  • Antibacterial Activities and Molecular Docking of Novel Sulfone Biscompound Containing Bioactive 1,2,3-Triazole Moiety

    Antibacterial Activities and Molecular Docking of Novel Sulfone Biscompound Containing Bioactive 1,2,3-Triazole Moiety

  • 6-Veterinary-Medicinal-Products-Criteria-Designation-Antimicrobials-Be-Reserved-Treatment

    6-Veterinary-Medicinal-Products-Criteria-Designation-Antimicrobials-Be-Reserved-Treatment

  • Antibiotic Uptake Across Gram-Negative Outer Membranes: Better Predictions Towards Better Antibiotics

    Antibiotic Uptake Across Gram-Negative Outer Membranes: Better Predictions Towards Better Antibiotics

  • New Aminocoumarin Antibiotics Derived from 4-Hydroxycinnamic

    New Aminocoumarin Antibiotics Derived from 4-Hydroxycinnamic

  • WO 2010/083148 Al

    WO 2010/083148 Al

  • Watching Antibiotics in Action: Exploiting Time-Lapse Microfluidic Microscopy As a Tool for Target-Drug Interaction Studies in Mycobacterium

    Watching Antibiotics in Action: Exploiting Time-Lapse Microfluidic Microscopy As a Tool for Target-Drug Interaction Studies in Mycobacterium

  • Front Matter

    Front Matter

  • Mycobacterium Tuberculosis DNA Gyrase As a Target for Drug Discovery

    Mycobacterium Tuberculosis DNA Gyrase As a Target for Drug Discovery

  • Thiazoles As Novel DNA Gyrase Inhibitors

    Thiazoles As Novel DNA Gyrase Inhibitors

  • Repurposing Potential of Diminazene Aceturate As an Inhibitor of the E

    Repurposing Potential of Diminazene Aceturate As an Inhibitor of the E

  • Sweet Spot of a Killer

    Sweet Spot of a Killer

  • Designing Type II Topoisomerase Inhibitors: a Molecular Modeling Approach

    Designing Type II Topoisomerase Inhibitors: a Molecular Modeling Approach

  • Molecular and Biochemical Investigation of the Biosynthesis of Clorobiocin in Streptomyces Roseochromogenes DS 12.976

    Molecular and Biochemical Investigation of the Biosynthesis of Clorobiocin in Streptomyces Roseochromogenes DS 12.976

Top View
  • Biosynthesis of the Antibiotic Mupirocin by Pseudomonas Fluorescens Ncimb 10586
  • WO 2009/106211 Al
  • (12) United States Patent (10) Patent No.: US 9,642,858 B2 Horzempa Et Al
  • Download Product Insert (PDF)
  • Author Index Volume 142
  • Cloq, a Prenyltransferase Involved in Clorobiocin Biosynthesis
  • Effect of E. Coli Topa Mutation on SOS and Antibiotic Response
  • A Promising Weapon in the Arsenal Against Antibiotic-Resistant Bacteria
  • New Aminocoumarin Antibiotics from a Cloq-Defective Mutant of the Clorobiocin
  • Q06004.Pdf (2.756Mb)
  • Antibacterial Agents: 1,4-Disubstituted 1,2,3-Triazole Analogs of the Oxazolidinone a Dissertation Presented to the Faculty Of
  • Comparison of Antibiotic Resistance Mechanisms in Antibiotic-Producing and Pathogenic Bacteria
  • W O 2019/074870 a L 18 April 2019 (18.04.2019) W 1P O PCT
  • A High-Throughput Screen for Directed Evolution of Aminocoumarin Amide Synthetases ⇑ Niranjan Parajuli, Gavin J
  • 21St ISCB International Conference (ISCBC-2015)
  • Clorobiocin Biosynthesis in Streptomyces: Identification of the Halogenase and Generation of Structural Analogs
  • Expanding the Potential of Mutasynthetic Approaches for Pseudomonic Acids
  • Quinolone Synthesis


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