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Volumn 161, Issue 7, 2010, Pages 526-533

Heterologous production of ribostamycin derivatives in engineered Escherichia coli

Author keywords

2 Deoxystreptamine; Aminoglycosides; Co expression; Eengineered Escherichia coli; Heterologous production

Indexed keywords

2 DEOXYSTREPTAMINE; AMINOGLYCOSIDE; OXIDOREDUCTASE; PAROMAMINE; PSEUDORIBOSTAMYCIN; RIBOSTAMYCIN; UNCLASSIFIED DRUG;

EID: 77956281445     PISSN: 09232508     EISSN: 17697123     Source Type: Journal    
DOI: 10.1016/j.resmic.2010.04.013     Document Type: Article
Times cited : (5)

References (32)
  • 2
    • 70349452052 scopus 로고    scopus 로고
    • Structural and functional aspects of the multidrug efflux pump AcrB
    • Eicher T., Brandsätter L., Pos K.M. Structural and functional aspects of the multidrug efflux pump AcrB. Biol. Chem. 2009, 390:693-699.
    • (2009) Biol. Chem. , vol.390 , pp. 693-699
    • Eicher, T.1    Brandsätter, L.2    Pos, K.M.3
  • 3
    • 0037545559 scopus 로고    scopus 로고
    • Production of plant-specific flavanones by Escherichia coli containing an artificial gene cluster
    • Hwang E.I., Kaneko M., Ohnishi Y., Horinouchi S. Production of plant-specific flavanones by Escherichia coli containing an artificial gene cluster. Appl. Environ. Microbiol. 2003, 69:2699-2706.
    • (2003) Appl. Environ. Microbiol. , vol.69 , pp. 2699-2706
    • Hwang, E.I.1    Kaneko, M.2    Ohnishi, Y.3    Horinouchi, S.4
  • 4
    • 33644547013 scopus 로고    scopus 로고
    • Molecular understanding of aminoglycoside action and resistance
    • Jana S., Deb J.K. Molecular understanding of aminoglycoside action and resistance. Appl. Microbiol. Biotechnol. 2006, 70:140-150.
    • (2006) Appl. Microbiol. Biotechnol. , vol.70 , pp. 140-150
    • Jana, S.1    Deb, J.K.2
  • 5
    • 34250304606 scopus 로고    scopus 로고
    • Synthesis of unnatural flavonoids and stilbenes by exploiting the plant biosynthetic pathway in Escherichia coli
    • Katsuyama Y., Funa N., Miyahisa I., Horinouchi S. Synthesis of unnatural flavonoids and stilbenes by exploiting the plant biosynthetic pathway in Escherichia coli. Chem. Biol. 2007, 14:613-621.
    • (2007) Chem. Biol. , vol.14 , pp. 613-621
    • Katsuyama, Y.1    Funa, N.2    Miyahisa, I.3    Horinouchi, S.4
  • 6
    • 53449086128 scopus 로고    scopus 로고
    • Production of curcuminoids by Escherichia coli carrying an artificial biosynthesis pathway
    • Katsuyama Y., Matsuzawa M., Funa N. Production of curcuminoids by Escherichia coli carrying an artificial biosynthesis pathway. Microbiology 2008, 154:2620-2628.
    • (2008) Microbiology , vol.154 , pp. 2620-2628
    • Katsuyama, Y.1    Matsuzawa, M.2    Funa, N.3
  • 7
    • 0034426097 scopus 로고    scopus 로고
    • Aminoglycosides: perspectives on mechanisms of action and resistance and strategies to counter resistance
    • Kotra L.P., Haddad J., Mobashery S. Aminoglycosides: perspectives on mechanisms of action and resistance and strategies to counter resistance. Antimicrob. Agents. Chemother. 2000, 44:3249-3256.
    • (2000) Antimicrob. Agents. Chemother. , vol.44 , pp. 3249-3256
    • Kotra, L.P.1    Haddad, J.2    Mobashery, S.3
  • 8
    • 64049089984 scopus 로고    scopus 로고
    • Biosynthetic enzymes for the aminoglycosides butirosin and neomycin
    • Kudo F., Eguchi T. Biosynthetic enzymes for the aminoglycosides butirosin and neomycin. Methods Enzymol. 2009, 459:493-519.
    • (2009) Methods Enzymol. , vol.459 , pp. 493-519
    • Kudo, F.1    Eguchi, T.2
  • 9
    • 34248652943 scopus 로고    scopus 로고
    • Unique O-ribosylation in the biosynthesis of butirosin
    • Kudo F., Fujii T., Kinoshita S., Eguchi T. Unique O-ribosylation in the biosynthesis of butirosin. Bioorg. Med. Chem. 2007, 15:4360-4368.
    • (2007) Bioorg. Med. Chem. , vol.15 , pp. 4360-4368
    • Kudo, F.1    Fujii, T.2    Kinoshita, S.3    Eguchi, T.4
  • 10
    • 31444455929 scopus 로고    scopus 로고
    • Biosynthesis of 2-deoxystreptamine by three crucial enzymes in Streptomyces fradiae NBRC 12773
    • Kudo F., Yamamoto Y., Yokoyama K., Eguchi T., Kakinuma K. Biosynthesis of 2-deoxystreptamine by three crucial enzymes in Streptomyces fradiae NBRC 12773. J. Antibiot. 2005, 58:766-774.
    • (2005) J. Antibiot. , vol.58 , pp. 766-774
    • Kudo, F.1    Yamamoto, Y.2    Yokoyama, K.3    Eguchi, T.4    Kakinuma, K.5
  • 11
    • 77950671878 scopus 로고    scopus 로고
    • Biosynthesis of paromamine derivatives in engineered Escherichia coli by heterologous expression
    • Kurumbang N.P., Liou K., Sohng J.K. Biosynthesis of paromamine derivatives in engineered Escherichia coli by heterologous expression. J. Appl. Microbiol. 2009, 10.1111/j.1365-2672.2009.04582.x.
    • (2009) J. Appl. Microbiol.
    • Kurumbang, N.P.1    Liou, K.2    Sohng, J.K.3
  • 12
    • 50249136479 scopus 로고    scopus 로고
    • Heterologous production and detection of recombinant directing 2-deoxystreptamine (DOS) in the non-aminoglycoside-producing host Streptomyces venezuelae YJ003
    • Kurumbang N.P., Oh T.J., Liou K., Sohng J.K. Heterologous production and detection of recombinant directing 2-deoxystreptamine (DOS) in the non-aminoglycoside-producing host Streptomyces venezuelae YJ003. J. Microbiol. Biotechnol. 2008, 18:866-873.
    • (2008) J. Microbiol. Biotechnol. , vol.18 , pp. 866-873
    • Kurumbang, N.P.1    Oh, T.J.2    Liou, K.3    Sohng, J.K.4
  • 13
    • 3342967467 scopus 로고    scopus 로고
    • Deoxystreptamine dimers bind to RNA hairpin loops
    • Liu X., Thomas J.R., Hergenrother P.J. Deoxystreptamine dimers bind to RNA hairpin loops. J. Am. Chem. Soc. 2004, 126:9196-9197.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 9196-9197
    • Liu, X.1    Thomas, J.R.2    Hergenrother, P.J.3
  • 14
    • 33751325834 scopus 로고    scopus 로고
    • Biosynthesis of 2-deoxystreptamine-containing aminoglycoside antibiotics
    • Llewellyn N.M., Spencer J.B. Biosynthesis of 2-deoxystreptamine-containing aminoglycoside antibiotics. Nat. Prod. Rep. 2006, 23:864-874.
    • (2006) Nat. Prod. Rep. , vol.23 , pp. 864-874
    • Llewellyn, N.M.1    Spencer, J.B.2
  • 15
    • 49249130589 scopus 로고    scopus 로고
    • Chemoenzymatic acylation of aminoglycoside antibiotics
    • Llewellyn N.M., Spencer J.B. Chemoenzymatic acylation of aminoglycoside antibiotics. Chem. Commun. 2008, 32:3786-3788.
    • (2008) Chem. Commun. , vol.32 , pp. 3786-3788
    • Llewellyn, N.M.1    Spencer, J.B.2
  • 16
    • 14844348264 scopus 로고    scopus 로고
    • Molecular insights into aminoglycoside action and resistance
    • Magnet S., Blanchard J.S. Molecular insights into aminoglycoside action and resistance. Chem. Rev. 2005, 105:477-497.
    • (2005) Chem. Rev. , vol.105 , pp. 477-497
    • Magnet, S.1    Blanchard, J.S.2
  • 17
    • 66649109099 scopus 로고    scopus 로고
    • Heterologous production of paromamine in Streptomyces lividans TK24 using kanamycin biosynthetic genes from Streptomyces kanamyceticus ATCC12853
    • Nepal K.K., Oh T.J., Subba B., Yoo J.C., Sohng J.K. Heterologous production of paromamine in Streptomyces lividans TK24 using kanamycin biosynthetic genes from Streptomyces kanamyceticus ATCC12853. Mol. Cells 2009, 27:83-88.
    • (2009) Mol. Cells , vol.27 , pp. 83-88
    • Nepal, K.K.1    Oh, T.J.2    Subba, B.3    Yoo, J.C.4    Sohng, J.K.5
  • 18
    • 0030029513 scopus 로고    scopus 로고
    • AcrAB efflux pump plays a major role in the antibiotic resistance phenotype of Escherichia coli multiple-antibiotic-resistance (Mar) mutants
    • Okusu H., Ma D., Nikaido H. AcrAB efflux pump plays a major role in the antibiotic resistance phenotype of Escherichia coli multiple-antibiotic-resistance (Mar) mutants. J. Bacteriol. 1996, 178:306-308.
    • (1996) J. Bacteriol. , vol.178 , pp. 306-308
    • Okusu, H.1    Ma, D.2    Nikaido, H.3
  • 21
    • 1542563485 scopus 로고
    • Evolutionary and structure relationship among dehydrogenases
    • Academic Press, New York, P.D. Boyer (Ed.)
    • Rossmann M.G., Lilias A., Branden C.I., Banaszak L.K. Evolutionary and structure relationship among dehydrogenases. The Enzymes: Oxidation-reduction 1975, 61-102. Academic Press, New York. P.D. Boyer (Ed.).
    • (1975) The Enzymes: Oxidation-reduction , pp. 61-102
    • Rossmann, M.G.1    Lilias, A.2    Branden, C.I.3    Banaszak, L.K.4
  • 23
    • 31444453703 scopus 로고    scopus 로고
    • The ribostamycin biosynthetic gene cluster in Streptomyces ribosidificus: comparison with butirosin biosynthesis
    • Subba B., Kharel M.K., Lee H.C., Liou K., Kim B.G., Sohng J.K. The ribostamycin biosynthetic gene cluster in Streptomyces ribosidificus: comparison with butirosin biosynthesis. Mol. Cells 2005, 20:90-96.
    • (2005) Mol. Cells , vol.20 , pp. 90-96
    • Subba, B.1    Kharel, M.K.2    Lee, H.C.3    Liou, K.4    Kim, B.G.5    Sohng, J.K.6
  • 25
    • 34648813081 scopus 로고    scopus 로고
    • Heterologous expression of the kanamycin biosynthetic gene cluster (pSKC2) in Streptomyces venezuelae YJ003
    • Thapa L.P., Oh T.J., Lee H.C., Liou K., Park J.W., Yoon Y.J., Sohng J.K. Heterologous expression of the kanamycin biosynthetic gene cluster (pSKC2) in Streptomyces venezuelae YJ003. Appl. Microbiol. Biotechnol. 2007, 76:1357-1364.
    • (2007) Appl. Microbiol. Biotechnol. , vol.76 , pp. 1357-1364
    • Thapa, L.P.1    Oh, T.J.2    Lee, H.C.3    Liou, K.4    Park, J.W.5    Yoon, Y.J.6    Sohng, J.K.7
  • 26
    • 3242890387 scopus 로고    scopus 로고
    • Interactions underlying assembly of the Escherichia coli AcerAC-TolC multidrug efflux system
    • Touzé T., Eswaran J., Bokma E., Koronakis E., Hughes C., Koronakis V. Interactions underlying assembly of the Escherichia coli AcerAC-TolC multidrug efflux system. Mol. Microbiol. 2004, 53:697-706.
    • (2004) Mol. Microbiol. , vol.53 , pp. 697-706
    • Touzé, T.1    Eswaran, J.2    Bokma, E.3    Koronakis, E.4    Hughes, C.5    Koronakis, V.6
  • 27
    • 65349153338 scopus 로고    scopus 로고
    • Diversification of echinomycin molecular structure by way of chemoenzymatic synthesis and heterologous expression of the engineered echinomycin biosynthetic pathway
    • Watanabe K., Oguri H., Oikawa H. Diversification of echinomycin molecular structure by way of chemoenzymatic synthesis and heterologous expression of the engineered echinomycin biosynthetic pathway. Curr. Opin. Chem. Biol. 2009, 13:189-196.
    • (2009) Curr. Opin. Chem. Biol. , vol.13 , pp. 189-196
    • Watanabe, K.1    Oguri, H.2    Oikawa, H.3
  • 28
    • 0041691117 scopus 로고    scopus 로고
    • Engineered biosynthesis of an ansamycin polyketide precursor in Escherichia coli
    • Watanabe K., Rude M.A., Walsh C.T., Khosla C. Engineered biosynthesis of an ansamycin polyketide precursor in Escherichia coli. Proc. Natl. Acad.Sci. USA 2003, 100:9774-9778.
    • (2003) Proc. Natl. Acad.Sci. USA , vol.100 , pp. 9774-9778
    • Watanabe, K.1    Rude, M.A.2    Walsh, C.T.3    Khosla, C.4
  • 29
    • 64049096163 scopus 로고    scopus 로고
    • Enzymology of aminoglycoside biosynthesis-deduction from gene clusters
    • Wehmeier U., Piepersberg W. Enzymology of aminoglycoside biosynthesis-deduction from gene clusters. Methods Enzymol. 2009, 459:459-491.
    • (2009) Methods Enzymol. , vol.459 , pp. 459-491
    • Wehmeier, U.1    Piepersberg, W.2
  • 30
    • 17744378979 scopus 로고    scopus 로고
    • Stereochemical recognition of doubly functional aminotransferase in 2-deoxystreptamine biosynthesis
    • Yokoyama K., Kudo F., Kuwahara M., Inomata K., Tamegai H., Eguchi T., Kakinuma K. Stereochemical recognition of doubly functional aminotransferase in 2-deoxystreptamine biosynthesis. J. Am. Chem. Soc. 2005, 127:5869-5874.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 5869-5874
    • Yokoyama, K.1    Kudo, F.2    Kuwahara, M.3    Inomata, K.4    Tamegai, H.5    Eguchi, T.6    Kakinuma, K.7
  • 31
    • 37049024768 scopus 로고    scopus 로고
    • Characterization and mechanistic study of a radical SAM dehydrogenase in the biosynthesis of butirosin
    • Yokoyama K., Numakura M., Kudo F., Ohmori D., Eguchi T. Characterization and mechanistic study of a radical SAM dehydrogenase in the biosynthesis of butirosin. J. Am. Chem. Soc. 2007, 129:15147-15155.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 15147-15155
    • Yokoyama, K.1    Numakura, M.2    Kudo, F.3    Ohmori, D.4    Eguchi, T.5
  • 32
    • 34247593152 scopus 로고    scopus 로고
    • Modifications of aminoglycoside antibiotics targeting RNA
    • Zhou J., Wang G., Zhang L.H., Ye X.S. Modifications of aminoglycoside antibiotics targeting RNA. Med. Res. Rev. 2007, 27:279-316.
    • (2007) Med. Res. Rev. , vol.27 , pp. 279-316
    • Zhou, J.1    Wang, G.2    Zhang, L.H.3    Ye, X.S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.