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Hygromycin B

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Hygromycin B
Clinical data
Trade namesHygromix
Other namesO-6-Amino-6-deoxy-L-glycero-D-galacto-heptopyranosylidene-(1-2-3)-O-β-D-talopyranosyl(1-5)-2-deoxy-N3-methyl-D-streptamine, HYG
AHFS/Drugs.comInternational Drug Names
ATC code
  • none
Identifiers
  • (3'R,3aS,4S,4'R,5'R,6R,6'R,7S,7aS)-4-{[(1R,2S,3R,5S,6R)-3-amino-2,6-dihydroxy-5-(methylamino)cyclohexyl]oxy}-6'-[(1S)-1-amino-2-hydroxyethyl]-6-(hydroxymethyl)-tetrahydro-3aH-spiro[[1,3]dioxolo[4,5-c]pyran-2,2'-oxane]-3',4',5',7-tetrol
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.045.935Edit this at Wikidata
Chemical and physical data
FormulaC20H37N3O13
Molar mass527.524 g·mol−1
3D model (JSmol)
Melting point160 to 180 °C (320 to 356 °F) (decomp.)
  • O1[C@H]4[C@@H](OC12O[C@@H]([C@H](O)[C@@H](O)[C@H]2O)[C@@H](N)CO)[C@@H](O)[C@H](O[C@H]4O[C@@H]3[C@@H](O)[C@H](N)C[C@H](NC)[C@H]3O)CO
  • InChI=1S/C20H37N3O13/c1-23-7-2-5(21)9(26)15(10(7)27)33-19-17-16(11(28)8(4-25)32-19)35-20(36-17)18(31)13(30)12(29)14(34-20)6(22)3-24/h5-19,23-31H,2-4,21-22H2,1H3/t5-,6+,7+,8-,9+,10-,11+,12-,13-,14-,15-,16+,17+,18-,19+,20?/m1/s1 checkY
  • Key:GRRNUXAQVGOGFE-KPBUCVLVSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Hygromycin B is anantibiotic produced by thebacteriumStreptomyces hygroscopicus. It is anaminoglycoside that killsbacteria,fungi and othereukaryotic cells by inhibitingprotein synthesis.[1]

History

[edit]

Hygromycin B was originally developed in the 1950s for use with animals and is still added into swine and chicken feed as ananthelmintic or anti-worming agent (product name: Hygromix). Hygromycin B is produced byStreptomyces hygroscopicus, a bacterium isolated in 1953 from a soil sample. Resistance genes were discovered in the early 1980s.[2][3]

Mechanism of action

[edit]

Hygromycin B, along with aminoglycosides, inhibits protein synthesis by strengthening the interaction of tRNA binding in the ribosomal A-site. Hygromycin B also prevents mRNA and tRNA translocation by an unknown mechanism.[4]

Use in research

[edit]

In the laboratory it is used for the selection and maintenance of prokaryotic and eukaryotic cells that contain the hygromycinresistance gene. The resistance gene is akinase that inactivates hygromycin B throughphosphorylation.[5] Since the discovery of hygromycin-resistance genes, hygromycin B has become a standard selection antibiotic in gene transfer experiments in many prokaryotic and eukaryotic cells. Based on impurity monitor method,[6] four different kinds of impurities are discovered in commercial hygromycin B from different suppliers and toxicities of different impurities to the cell lines are described in the following external links.[citation needed]

FungusConiothyrium minitans was transformed with the hygromycin B resistance gene to improve the infection rates ofSclerotinia sclerotiorum, a fungal parasite of many crops.[7]

Use in plant research

[edit]

Hygromycinresistancegene is frequently used as aselectable marker in research onplants. InriceAgrobacterium-mediatedtransformation system, hygromycin is used at about 30–75 mg L−1, with an average of 50 mg L−1. The use of hygromycin at 50 mg L−1 demonstrated highlytoxic to non-transformedcalli. Thus, it can be efficiently used to selecttransformants.[8]

References

[edit]
  1. ^Pittenger RC, Wolfe RN, Hoehn MM, Marks PN, Daily WA, McGUIRE JM (December 1953). "Hygromycin. I. Preliminary studies on the production and biologic activity of a new antibiotic".Antibiotics & Chemotherapy.3 (12):1268–1278.PMID 24542808.
  2. ^Gritz L, Davies J (November 1983). "Plasmid-encoded hygromycin B resistance: the sequence of hygromycin B phosphotransferase gene and its expression inEscherichia coli andSaccharomyces cerevisiae".Gene.25 (2–3):179–188.doi:10.1016/0378-1119(83)90223-8.PMID 6319235.
  3. ^Kaster KR, Burgett SG, Rao RN, Ingolia TD (October 1983)."Analysis of a bacterial hygromycin B resistance gene by transcriptional and translational fusions and by DNA sequencing".Nucleic Acids Research.11 (19):6895–6911.doi:10.1093/nar/11.19.6895.PMC 326422.PMID 6314265.
  4. ^"Hygromycin B".TOKU-E. Retrieved2024-06-28.
  5. ^Rao RN, Allen NE, Hobbs JN, Alborn WE, Kirst HA, Paschal JW (November 1983)."Genetic and enzymatic basis of hygromycin B resistance inEscherichia coli".Antimicrobial Agents and Chemotherapy.24 (5):689–695.doi:10.1128/aac.24.5.689.PMC 185926.PMID 6318654.
  6. ^Kauffman JS (2009). "Analytical Strategies for Monitoring Residual Impurities Best methods to monitor product-related impurities throughout the production process".BioPharm International.23:1–3.
  7. ^Jones EE, Stewart A, Whipps JM (March 2003)."Use ofConiothyrium minitans transformed with the hygromycin B resistance gene to study survival and infection ofSclerotinia sclerotiorum sclerotia in soil"(PDF).Mycological Research.107 (Pt 3):267–276.doi:10.1017/S0953756203007457.PMID 12825495.
  8. ^Pazuki A, Asghari J, Sohani MM, Pessarakli M, Aflaki F (2014)."Effects of Some Organic Nitrogen Sources and Antibiotics on Callus Growth of Indica Rice Cultivars"(PDF).Journal of Plant Nutrition.38 (8):1231–1240.doi:10.1080/01904167.2014.983118.S2CID 84495391. RetrievedNovember 17, 2014.
30S
Aminoglycosides
(initiation inhibitors)
-mycin (Streptomyces)
-micin (Micromonospora)
other
Tetracycline antibiotics
(tRNA binding)
Tetracyclines
Glycylcyclines
50S
Oxazolidinone
(initiation inhibitors)
Peptidyl transferase
Amphenicols
MLS (transpeptidation/translocation)
Macrolides
Azalides
Ketolides
Lincosamides
Oxepanoprolinamides
Streptogramins
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