When was kanamycin discovered




















Grete Kellenberger-Gujer: molecular biology research pioneer. Bacteriophage 6 , e Benveniste, R. Aminoglycoside antibiotic-inactivating enzymes in actinomycetes similar to those present in clinical isolates of antibiotic-resistant bacteria. USA 70 , — Huang, A. Defective interfering viruses. Berg, P. Personal reflections on the origins and emergence of recombinant DNA technology. Genetics , 9—17 Chang, A. Genome construction between bacterial species in vitro : replication and expression of Staphylococcus plasmid genes in Escherichia coli.

USA 71 , — Jackson, D. USA 69 , — Isolation of a lambda dv plasmid carrying the bacterial gal operon. Shimada, K. Prophage lambda at unusual chromosomal locations. Location of the secondary attachment sites and the properties of the lysogens. Umezawa, H. Phosphorylation and inactivation of kanamycin by Pseudomonas aeruginosa.

Tokyo 21 , — Okanishi, K. Phosphorylation and inactivation of aminoglycosidic antibiotics by E. Tokyo 21 , 13—21 Yagisawa, M. Tokyo 25 , — Brzezinska, M. Two enzymes which phosphorylate neomycin and kanamycin in Escherichia coli strains carrying R factors. Agents Chemother. McClintock, B. The origin and behavior of mutable loci in maize. USA 36 , — Controlling elements and the gene. The significance of responses of the genome to challenge.

Science , — Feng, S. Epigenetic reprogramming in plant and animal development. Levin, H. Dynamic interactions between transposable elements and their hosts. Sundaram, V. Widespread contribution of transposable elements to the innovation of gene regulatory networks. Genome Res. Taylor, A. Bacteriophage-induced mutation In Escherichia coli. USA 50 , — Harshey, R. Transposable Phage Mu. Michaelis, G. Two insertions in the galactose operon having different sizes but homologous DNA sequences.

Saedler, H. Shapiro, J. Mutations caused by the insertion of genetic material into the galactose operon of Escherichia coli. Campbell, A. Nomenclature of transposable elements in prokaryotes.

Gene 5 , — Berg, C. Jorgensen, R. Restriction enzyme cleavage map of Tn 10 , a transposon which encodes tetracycline resistance. Reznikoff, W.

Transposon Tn5. Accessed on 26 August Haniford, D. Transposons Tn 10 and Tn 5. Thoughts on the origins of resistance plasmids.

Structural requirement for ISmediated gene transposition. USA 80 , — Molecular model for the transposition and replication of bacteriophage Mu and other transposable elements. Siguier, P. Everyman's Guide to Bacterial Insertion Sequences. Spectr 3 , MDNA PubMed Google Scholar.

Stibitz, S. Use of conditionally counterselectable suicide vectors for allelic exchange. Methods Enzymol. Taylor, D. Genetics of Campylobacter and Helicobacter. Sugden, B. Transforming functions associated with Epstein-Barr virus. Datta, K. Methods Mol. Wang, T. Transformation systems of non- Saccharomyces yeasts. Messina, M. Stable DNA transformation of Toxoplasma gondii using phleomycin selection. Gene , — Guerrero, C. The bleomycin resistance gene of transposon Tn5 is an excellent marker for transformation of corynebacteria.

Marshall, B. The relation of Helicobacter pylori to gastric adenocarcinoma and lymphoma: pathophysiology, epidemiology, screening, clinical presentation, treatment, and prevention. North Am. PubMed Article Google Scholar. Waksman, S. Neomycin, a new antibiotic active against streptomycin-resistant bacteria, including tuberculosis organisms. Howells, J. Butirosin, a new aminoglycosidic antibiotic complex: bacterial origin and some microbiological studies.

Fischbach, M. Antibiotics for emerging pathogens. Kondo, S. Semisynthetic aminoglycoside antibiotics: development and enzymatic modifications. Kudo, F. Biosynthetic enzymes for the aminoglycosides butirosin and neomycin.

Methods Enzymol. Molecular cloning of the gene for the key carbohydrate-forming enzyme in the biosynthesis of 2-deoxystreptamine-containing aminocyclitol antibiotics and its comparison with dehydroquinate synthase.

Tokyo 52 , — Huang, F. The neomycin biosynthetic gene cluster of Streptomyces fradiae NCIMB characterisation of an aminotransferase involved in the formation of 2-deoxystreptamine. Tokyo 58 , — Wehmeier, U. Enzymology of aminoglycoside biosynthesis-deduction from gene clusters. Fan, Q. The neomycin biosynthetic gene cluster of Streptomyces fradiae NCIMB genetic and biochemical evidence for the roles of two glycosyltransferases and a deacetylase.

Park, J. Genetic dissection of the biosynthetic route to gentamicin A2 by heterologous expression of its minimal gene set. USA , — Truman, A. Characterization of the enzyme BtrD from Bacillus circulans and revision of its functional assignment in the biosynthesis of butirosin. Edn Engl. Thuy, M. Expression of 2-deoxy- scyllo -inosose synthase kanA from kanamycin gene cluster in Streptomyces lividans. Jnawali, H. Nepal, K. Cells 27 , — Enzymatic activity of a glycosyltransferase KanM2 encoded in the kanamycin biosynthetic gene cluster.

Tokyo 62 , — Kojima, M. Studies on the biosynthesis of kanamycins. Part I. Incorporation of 14 C-glucose or 14 C-glucosamine into kanamycins and kanamycin-related compounds. Part II.

Incorporation of the radioactive degradation products of kanamycin A or related metabolites into kanamycin A. Llewellyn, N. Biosynthesis of 2-deoxystreptamine-containing aminoglycoside antibiotics.

Piepersberg, W. Arya, D. Biosynthetic genes for aminoglycoside antibiotics. Kharel, M. A gene cluster for biosynthesis of kanamycin from Streptomyces kanamyceticus : comparison with gentamicin biosynthetic gene cluster. Thapa, L. Lemieux, R. The synthesis of kanamycin analogs. Further research is needed to establish safety and efficacy in infants.

Further research is needed to establish safety and efficacy when combined with antiretrovirals that may cause renal failure such as tenofovir. Manufacturers and suppliers:. Today, only three kanamycin products approved by a stringent regulatory authority have been identified. No sources of kanamycin are approved through WHO Prequalification, although one manufacturer Macleods has submitted a dossier to WHO Prequalification and has been accepted for evaluation.

Despite this, the supply of kanamycin remains vulnerable to disruption. In the EU, there is only one approved manufacturer Panpharma but in they had a problem with the API, resulting in an interruption in supply.

As this was the only quality-assured source available to GDF at the time, this resulted in a significant problem for GLC-approved programmes and other treatment providers. The problem has been rectified but capacity issues remain. In reaction to the potential shortage of quality-assured kanamycin, GDF identified an alternative source in Japan Meiji. While this has helped to ensure continual supply while Panpharma was not in production, Meiji has limited production capacity and the price is considerably more than the Panpharma product.

The supply is also reserved for GDF, leaving other treatment providers with no alternative quality-assured sources. Additional manufacturers may exist in China, India, the former Soviet Union, and other countries, but whether they comply with WHO quality standards is unknown.

Efficacy and safety of kanamycin, ethionamide, PAS and cycloserine in multidrug-resistant pulmonary tuberculosis patients. Best drug treatment for multidrug-resistant and extensively drug-resistant tuberculosis. Lancet Infect Dis.



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