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Volumn 8, Issue 1, 2017, Pages

Biosynthesis of ilamycins featuring unusual building blocks and engineered production of enhanced anti-tuberculosis agents

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINO 4 HEXENOIC ACID; 3 NITROTYROSINE; ANTIMYCOBACTERIAL AGENT; ILAMYCIN DERIVATIVE; SHORT CHAIN FATTY ACID; TUBERCULOSTATIC AGENT; UNCLASSIFIED DRUG; 3-NITROTYROSINE; CYCLOPEPTIDE; TYROSINE;

EID: 85028561302     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/s41467-017-00419-5     Document Type: Article
Times cited : (102)

References (59)
  • 2
    • 85028550541 scopus 로고    scopus 로고
    • World Health Organization. Global tuberculosis report
    • World Health Organization. Global tuberculosis report, http://www.who.int/tb/publications/global-report/en/(2015).
    • (2015)
  • 3
    • 85011006728 scopus 로고    scopus 로고
    • Drug regimens identified and optimized by output-driven platform markedly reduce tuberculosis treatment time
    • Lee, B.-Y. et al. Drug regimens identified and optimized by output-driven platform markedly reduce tuberculosis treatment time. Nat. Commun. 8, 14183 (2017).
    • (2017) Nat. Commun. , vol.8 , pp. 14183
    • Lee, B.-Y.1
  • 4
    • 84867742983 scopus 로고    scopus 로고
    • Unexpected high levels of multidrug-resistant tuberculosis present new challenges for tuberculosis control
    • Hoffner, S. Unexpected high levels of multidrug-resistant tuberculosis present new challenges for tuberculosis control. Lancet 380, 1367-1369 (2012).
    • (2012) Lancet , vol.380 , pp. 1367-1369
    • Hoffner, S.1
  • 5
    • 84856115626 scopus 로고    scopus 로고
    • India reports cases of totally drug-resistant tuberculosis
    • Loewenberg, S. India reports cases of totally drug-resistant tuberculosis. Lancet 379, 205 (2012).
    • (2012) Lancet , vol.379 , pp. 205
    • Loewenberg, S.1
  • 6
    • 84925882714 scopus 로고    scopus 로고
    • Cytotoxic and antibacterial angucycline-and prodigiosin-analogues from the deep-sea derived Streptomyces sp. SCSIO 11594
    • Song, Y. et al. Cytotoxic and antibacterial angucycline-and prodigiosin-analogues from the deep-sea derived Streptomyces sp. SCSIO 11594. Mar. Drugs 13, 1304-1316 (2015).
    • (2015) Mar. Drugs , vol.13 , pp. 1304-1316
    • Song, Y.1
  • 7
    • 84906712570 scopus 로고    scopus 로고
    • Cyclic hexapeptides from the deep South China Sea-derived Streptomyces scopuliridis SCSIO ZJ46 active against pathogenic Gram-positive bacteria
    • Song, Y. et al. Cyclic hexapeptides from the deep South China Sea-derived Streptomyces scopuliridis SCSIO ZJ46 active against pathogenic Gram-positive bacteria. J. Nat. Prod. 77, 1937-1941 (2014).
    • (2014) J. Nat. Prod. , vol.77 , pp. 1937-1941
    • Song, Y.1
  • 8
    • 84871982232 scopus 로고    scopus 로고
    • Marthiapeptide A, an anti-infective and cytotoxic polythiazole cyclopeptide from a 60 L scale fermentation of the deep sea-derived Marinactinospora thermotolerans SCSIO 00652
    • Zhou, X. et al. Marthiapeptide A, an anti-infective and cytotoxic polythiazole cyclopeptide from a 60 L scale fermentation of the deep sea-derived Marinactinospora thermotolerans SCSIO 00652. J. Nat. Prod. 75, 2251-2255 (2012).
    • (2012) J. Nat. Prod. , vol.75 , pp. 2251-2255
    • Zhou, X.1
  • 10
    • 0345231192 scopus 로고
    • A study of the secondary structure of ilamycin B(1) by 300 MHz proton magnetic resonance
    • Cary, L. W., Takita, T. & Ohnishi, M. A study of the secondary structure of ilamycin B(1) by 300 MHz proton magnetic resonance. FEBS Lett. 17, 145-148 (1971).
    • (1971) FEBS Lett. , vol.17 , pp. 145-148
    • Cary, L.W.1    Takita, T.2    Ohnishi, M.3
  • 11
    • 0011281881 scopus 로고
    • An X-ray study of ilamycin B1, a cyclic heptapeptide antibiotic
    • Iitaka, Y., Nakamura, H., Takada, K. & Takita, T. An X-ray study of ilamycin B1, a cyclic heptapeptide antibiotic. Acta Crystallogr. B30, 2817-2825 (1974).
    • (1974) Acta Crystallogr. , vol.30 , pp. 2817-2825
    • Iitaka, Y.1    Nakamura, H.2    Takada, K.3    Takita, T.4
  • 15
    • 84877267006 scopus 로고    scopus 로고
    • Advances in the development of new tuberculosis drugs and treatment regimens
    • Zumla, A., Nahid, P. & Cole, S. T. Advances in the development of new tuberculosis drugs and treatment regimens. Nat. Rev. Drug Discov. 12, 388-404 (2013).
    • (2013) Nat. Rev. Drug Discov. , vol.12 , pp. 388-404
    • Zumla, A.1    Nahid, P.2    Cole, S.T.3
  • 16
    • 84896455574 scopus 로고    scopus 로고
    • New antituberculosis drugs, regimens, and adjunct therapies: Needs, advances, and future prospects
    • Zumla, A. I. et al. New antituberculosis drugs, regimens, and adjunct therapies: needs, advances, and future prospects. Lancet Infect. Dis. 14, 327-340 (2014).
    • (2014) Lancet Infect. Dis. , vol.14 , pp. 327-340
    • Zumla, A.I.1
  • 17
    • 84872403188 scopus 로고    scopus 로고
    • Abyssomicins from the South China Sea deep-sea sediment Verrucosispora sp.: Natural thioether Michael addition adducts as antitubercular prodrugs
    • Wang, Q. et al. Abyssomicins from the South China Sea deep-sea sediment Verrucosispora sp.: natural thioether Michael addition adducts as antitubercular prodrugs. Angew. Chem. Int. Ed. 52, 1231-1234 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 1231-1234
    • Wang, Q.1
  • 18
    • 84979859096 scopus 로고    scopus 로고
    • Antismash 3.0-a comprehensive resource for the genome mining of biosynthetic gene clusters
    • Weber, T. et al. Antismash 3.0-a comprehensive resource for the genome mining of biosynthetic gene clusters. Nucleic Acids Res. 43, W237-W243 (2015).
    • (2015) Nucleic Acids Res. , vol.43 , pp. W237-W243
    • Weber, T.1
  • 19
    • 0037452723 scopus 로고    scopus 로고
    • PCR-targeted Streptomyces gene replacement identifies a protein domain needed for biosynthesis of the sesquiterpene soil odor geosmin
    • Gust, B., Challis, G. L., Fowler, K., Kieser, T. & Chater, K. F. PCR-targeted Streptomyces gene replacement identifies a protein domain needed for biosynthesis of the sesquiterpene soil odor geosmin. Proc. Natl. Acad. Sci. USA 100, 1541-1546 (2003).
    • (2003) Proc. Natl. Acad. Sci. USA , vol.100 , pp. 1541-1546
    • Gust, B.1    Challis, G.L.2    Fowler, K.3    Kieser, T.4    Chater, K.F.5
  • 20
    • 80051740572 scopus 로고    scopus 로고
    • Biosynthesis of himastatin: Assembly line and characterization of three cytochrome P450 enzymes involved in the post-tailoring oxidative steps
    • Ma, J. et al. Biosynthesis of himastatin: assembly line and characterization of three cytochrome P450 enzymes involved in the post-tailoring oxidative steps. Angew. Chem. Int. Ed. 50, 7797-7802 (2011).
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 7797-7802
    • Ma, J.1
  • 21
    • 84954425816 scopus 로고    scopus 로고
    • Deciphering the biosynthetic origin of L-allo-isoleucine
    • Li, Q. et al. Deciphering the biosynthetic origin of L-allo-isoleucine. J. Am. Chem. Soc. 138, 408-415 (2016).
    • (2016) J. Am. Chem. Soc. , vol.138 , pp. 408-415
    • Li, Q.1
  • 22
    • 41549168666 scopus 로고    scopus 로고
    • Biosynthesis and structures of cyclomarins and cyclomarazines, prenylated cyclic peptides of marine actinobacterial origin
    • Schutlz, A. W. et al. Biosynthesis and structures of cyclomarins and cyclomarazines, prenylated cyclic peptides of marine actinobacterial origin. J. Am. Chem. Soc. 130, 4507-4516 (2008).
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 4507-4516
    • Schutlz, A.W.1
  • 23
    • 84918499989 scopus 로고    scopus 로고
    • Adenylation and S-methylation of cysteine by the bifunctional enzyme TioN in thiocoraline biosynthesis
    • Al-Mestarihi, A. H. et al. Adenylation and S-methylation of cysteine by the bifunctional enzyme TioN in thiocoraline biosynthesis. J. Am. Chem. Soc. 136, 17350-17354 (2014).
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 17350-17354
    • Al-Mestarihi, A.H.1
  • 24
    • 34249053161 scopus 로고    scopus 로고
    • MbtH-like protein-mediated cross-talk between non-ribosomal peptide antibiotic and siderophore biosynthetic pathways in Streptomyces coelicolor M145
    • Lautru, S., Oves-Costales, D., Pernodet, J.-L. & Challis, G. L. MbtH-like protein-mediated cross-talk between non-ribosomal peptide antibiotic and siderophore biosynthetic pathways in Streptomyces coelicolor M145. Microbiology 153, 1405-1412 (2007).
    • (2007) Microbiology , vol.153 , pp. 1405-1412
    • Lautru, S.1    Oves-Costales, D.2    Pernodet, J.-L.3    Challis, G.L.4
  • 25
    • 34249004256 scopus 로고    scopus 로고
    • Effects of deletions of mbtH-like genes on clorobiocin biosynthesis in Streptomyces coelicolor
    • Wolpert, M., Gust, B., Kammerer, B. & Heide, L. Effects of deletions of mbtH-like genes on clorobiocin biosynthesis in Streptomyces coelicolor. Microbiology 153, 1413-1423 (2007).
    • (2007) Microbiology , vol.153 , pp. 1413-1423
    • Wolpert, M.1    Gust, B.2    Kammerer, B.3    Heide, L.4
  • 26
    • 34547116228 scopus 로고    scopus 로고
    • The 1.8 A crystal structure of PA2412, an MbtH-like protein from the pyoverdine cluster of Pseudomonas aeruginosa
    • Drake, E. J. et al. The 1.8 A crystal structure of PA2412, an MbtH-like protein from the pyoverdine cluster of Pseudomonas aeruginosa. J. Biol. Chem. 282, 20425-20434 (2007).
    • (2007) J. Biol. Chem. , vol.282 , pp. 20425-20434
    • Drake, E.J.1
  • 27
    • 70350326295 scopus 로고    scopus 로고
    • Enzymatic tailoring of ornithine in the biosynthesis of the Rhizobium cyclic trihydroxamate siderophore vicibactin
    • Heemstra, J. R., Walsh, C. T. & Sattely, E. S. Enzymatic tailoring of ornithine in the biosynthesis of the Rhizobium cyclic trihydroxamate siderophore vicibactin. J. Am. Chem. Soc. 131, 15317-15329 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 15317-15329
    • Heemstra, J.R.1    Walsh, C.T.2    Sattely, E.S.3
  • 28
    • 38549152290 scopus 로고    scopus 로고
    • Substrate specificity of the acyl transferase domains of EpoC from the epothilone polyketide synthase
    • Petković, H. et al. Substrate specificity of the acyl transferase domains of EpoC from the epothilone polyketide synthase. Org. Biomol. Chem. 6, 500-506 (2008).
    • (2008) Org. Biomol. Chem. , vol.6 , pp. 500-506
    • Petković, H.1
  • 29
    • 84878928695 scopus 로고    scopus 로고
    • LovG: The thioesterase required for dihydromonacolin L release and lovastatin nonaketide synthase turnover in lovastatin biosynthesis
    • Xu, W. et al. LovG: the thioesterase required for dihydromonacolin L release and lovastatin nonaketide synthase turnover in lovastatin biosynthesis. Angew. Chem. Int. Ed. 52, 6472-6475 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 6472-6475
    • Xu, W.1
  • 30
    • 33748528639 scopus 로고    scopus 로고
    • Identification of NanE as the thioesterase for polyether chain release in nanchangmycin biosynthesis
    • Liu, T. et al. Identification of NanE as the thioesterase for polyether chain release in nanchangmycin biosynthesis. Chem. Biol. 13, 945-955 (2006).
    • (2006) Chem. Biol. , vol.13 , pp. 945-955
    • Liu, T.1
  • 31
    • 84904576107 scopus 로고    scopus 로고
    • Fungal polyketide synthase product chain-length control by partnering thiohydrolase
    • Zabala, A. O., Chooi, Y. H., Choi, M. S., Lin, H. C. & Tang, Y. Fungal polyketide synthase product chain-length control by partnering thiohydrolase. ACS Chem. Biol. 9, 1576-1586 (2014).
    • (2014) ACS Chem. Biol. , vol.9 , pp. 1576-1586
    • Zabala, A.O.1    Chooi, Y.H.2    Choi, M.S.3    Lin, H.C.4    Tang, Y.5
  • 32
    • 34547515662 scopus 로고    scopus 로고
    • Biosynthesis of nitro compounds
    • Winkler, R. & Hertweck, C. Biosynthesis of nitro compounds. ChemBioChem 8, 973-977 (2007).
    • (2007) ChemBioChem , vol.8 , pp. 973-977
    • Winkler, R.1    Hertweck, C.2
  • 33
    • 46649090918 scopus 로고    scopus 로고
    • Protein tyrosine nitration-functional alteration or just a biomarker?
    • Souza, J. M., Peluffo, G. & Radi, R. Protein tyrosine nitration-functional alteration or just a biomarker? Free Radic. Biol. Med. 45, 357-366 (2008).
    • (2008) Free Radic. Biol. Med. , vol.45 , pp. 357-366
    • Souza, J.M.1    Peluffo, G.2    Radi, R.3
  • 34
    • 26944469650 scopus 로고    scopus 로고
    • Effects of corticosteroids on noninvasive biomarkers of inflammation in asthma and chronic obstructive pulmonary disease
    • Kharitonov, S. A. & Barnes, P. J. Effects of corticosteroids on noninvasive biomarkers of inflammation in asthma and chronic obstructive pulmonary disease. Proc. Am. Thoracic Soc. 1, 191-199 (2004).
    • (2004) Proc. Am. Thoracic Soc. , vol.1 , pp. 191-199
    • Kharitonov, S.A.1    Barnes, P.J.2
  • 35
    • 25844457652 scopus 로고    scopus 로고
    • Biochemical markers and risk factors of Alzheimer's disease
    • Flirski, M. & Sobow, T. Biochemical markers and risk factors of Alzheimer's disease. Curr. Alzheimer Res. 2, 47-64 (2005).
    • (2005) Curr. Alzheimer Res. , vol.2 , pp. 47-64
    • Flirski, M.1    Sobow, T.2
  • 37
    • 84874037125 scopus 로고    scopus 로고
    • Protein tyrosine nitration: Biochemical mechanisms and structural basis of functional effects
    • Radi, R. Protein tyrosine nitration: biochemical mechanisms and structural basis of functional effects. Acc. Chem. Res. 46, 550-559 (2013).
    • (2013) Acc. Chem. Res. , vol.46 , pp. 550-559
    • Radi, R.1
  • 38
    • 2342621532 scopus 로고    scopus 로고
    • Nitration of a peptide phytotoxin by bacterial nitric oxide synthase
    • Kers, J. A. et al. Nitration of a peptide phytotoxin by bacterial nitric oxide synthase. Nature 429, 79-82 (2004).
    • (2004) Nature , vol.429 , pp. 79-82
    • Kers, J.A.1
  • 39
    • 84870301242 scopus 로고    scopus 로고
    • Cytochrome P450-catalyzed L-tryptophan nitration in thaxtomin phytotoxin biosynthesis
    • Barry, S. M. et al. Cytochrome P450-catalyzed L-tryptophan nitration in thaxtomin phytotoxin biosynthesis. Nat. Chem. Biol. 8, 814-816 (2012).
    • (2012) Nat. Chem. Biol. , vol.8 , pp. 814-816
    • Barry, S.M.1
  • 40
    • 0037963656 scopus 로고    scopus 로고
    • Nitroheterocyclic drugs with broad spectrum activity
    • Raether, W. & Hänel, H. Nitroheterocyclic drugs with broad spectrum activity. Parasitol. Res. 90, S19-S39 (2003).
    • (2003) Parasitol. Res. , vol.90 , pp. S19-S39
    • Raether, W.1    Hänel, H.2
  • 41
    • 1642388928 scopus 로고    scopus 로고
    • Biosynthetic origin of the rare nitroaryl moiety of the polyketide antibiotic aureothin: Involvement of an unprecedented N-oxygenase
    • He, J. & Hertweck, C. Biosynthetic origin of the rare nitroaryl moiety of the polyketide antibiotic aureothin: involvement of an unprecedented N-oxygenase. J. Am. Chem. Soc. 126, 3694-3695 (2004).
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 3694-3695
    • He, J.1    Hertweck, C.2
  • 42
    • 33845323336 scopus 로고    scopus 로고
    • OPC-67683, a nitro-dihydro-imidazooxazole derivative with promising action against tuberculosis in vitro and in mice
    • Matsumoto, M. et al. OPC-67683, a nitro-dihydro-imidazooxazole derivative with promising action against tuberculosis in vitro and in mice. PLoS Med. 3, e466 (2006).
    • (2006) PLoS Med. , vol.3 , pp. e466
    • Matsumoto, M.1
  • 43
    • 84868318849 scopus 로고    scopus 로고
    • Diversity of P450 enzymes in the biosynthesis of natural products
    • Podust, L. M. & Sherman, D. H. Diversity of P450 enzymes in the biosynthesis of natural products. Nat. Prod. Rep. 29, 1251-1266 (2012).
    • (2012) Nat. Prod. Rep. , vol.29 , pp. 1251-1266
    • Podust, L.M.1    Sherman, D.H.2
  • 44
    • 70549094244 scopus 로고    scopus 로고
    • Regioselective domino metathesis of unsymmetrical 7-oxanorbornenes with electron-rich vinyl acetate toward biologically active glutamate analogues
    • Oikawa, M. et al. Regioselective domino metathesis of unsymmetrical 7-oxanorbornenes with electron-rich vinyl acetate toward biologically active glutamate analogues. Eur. J. Org. Chem. 32, 5531-5548 (2009).
    • (2009) Eur. J. Org. Chem. , vol.32 , pp. 5531-5548
    • Oikawa, M.1
  • 46
    • 84937398809 scopus 로고    scopus 로고
    • Crystal structure refinement with SHELXL
    • Sheldrick, G. M. Crystal structure refinement with SHELXL. Acta Cryst. C71, 3-8 (2015).
    • (2015) Acta Cryst. , vol.71 , pp. 3-8
    • Sheldrick, G.M.1
  • 47
    • 37549039510 scopus 로고    scopus 로고
    • A short history of SHELX
    • Sheldrick, G. M. A short history of SHELX. Acta Cryst. A64, 112-122 (2008).
    • (2008) Acta Cryst. , vol.64 , pp. 112-122
    • Sheldrick, G.M.1
  • 48
    • 64249084052 scopus 로고    scopus 로고
    • Chapter 8. Methods for in silico prediction of microbial polyketide and nonribosomal peptide biosynthetic pathways from DNA sequence data
    • Bachmann, B. O. & Ravel, J. Chapter 8. Methods for in silico prediction of microbial polyketide and nonribosomal peptide biosynthetic pathways from DNA sequence data. Methods Enzymol. 458, 181-217 (2009).
    • (2009) Methods Enzymol. , vol.458 , pp. 181-217
    • Bachmann, B.O.1    Ravel, J.2
  • 49
    • 0033619244 scopus 로고    scopus 로고
    • A chain initiation factor common to both modular and aromatic polyketide synthases
    • Bisang, C. et al. A chain initiation factor common to both modular and aromatic polyketide synthases. Nature 401, 502-505 (1999).
    • (1999) Nature , vol.401 , pp. 502-505
    • Bisang, C.1
  • 50
    • 0032514668 scopus 로고    scopus 로고
    • A gene cluster for macrolide antibiotic biosynthesis in Streptomyces venezuelae: Architecture of metabolic diversity
    • Xue, Y., Zhao, L., Liu, H. W. & Sherman, D. H. A gene cluster for macrolide antibiotic biosynthesis in Streptomyces venezuelae: architecture of metabolic diversity. Proc. Natl. Acad. Sci. USA 9, 12111-12116 (1998).
    • (1998) Proc. Natl. Acad. Sci. USA , vol.9 , pp. 12111-12116
    • Xue, Y.1    Zhao, L.2    Liu, H.W.3    Sherman, D.H.4
  • 51
    • 79959378209 scopus 로고    scopus 로고
    • Reveromycin A biosynthesis uses RevG and RevJ for stereospecific spiroacetal formation
    • Takahashi, S. et al. Reveromycin A biosynthesis uses RevG and RevJ for stereospecific spiroacetal formation. Nat. Chem. Biol. 7, 461-468 (2011).
    • (2011) Nat. Chem. Biol. , vol.7 , pp. 461-468
    • Takahashi, S.1
  • 52
    • 26944480788 scopus 로고    scopus 로고
    • Molecular basis of Celmer's rules: Stereochemistry of catalysis by isolated ketoreductase domains from modular polyketide synthases
    • Siskos, A. P. et al. Molecular basis of Celmer's rules: stereochemistry of catalysis by isolated ketoreductase domains from modular polyketide synthases. Chem. Biol. 12, 1145-1153 (2005).
    • (2005) Chem. Biol. , vol.12 , pp. 1145-1153
    • Siskos, A.P.1
  • 53
    • 33644697200 scopus 로고    scopus 로고
    • Architecture of mammalian fatty acid synthase at 4.5 A resolution
    • Maier, T., Jenni, S. & Ban, N. Architecture of mammalian fatty acid synthase at 4.5 A resolution. Science 311, 1258-1262 (2006).
    • (2006) Science , vol.311 , pp. 1258-1262
    • Maier, T.1    Jenni, S.2    Ban, N.3
  • 54
    • 51149098989 scopus 로고    scopus 로고
    • The crystal structure of a mammalian fatty acid synthase
    • Maier, T., Leibundgut, M. & Ban, N. The crystal structure of a mammalian fatty acid synthase. Science 321, 1315-1322 (2008).
    • (2008) Science , vol.321 , pp. 1315-1322
    • Maier, T.1    Leibundgut, M.2    Ban, N.3
  • 55
    • 52949105378 scopus 로고    scopus 로고
    • The crystal structure of a mammalian fatty acid synthase
    • Knoll, M. & Pleiss, J. The crystal structure of a mammalian fatty acid synthase. Protein Sci. 17, 1689-1697 (2008).
    • (2008) Protein Sci. , vol.17 , pp. 1689-1697
    • Knoll, M.1    Pleiss, J.2
  • 56
    • 77956942908 scopus 로고    scopus 로고
    • Mutagenesis of a modular polyketide synthase enoylreductase domain reveals insights into catalysis and stereospecificity
    • Kwan, D. H. & Leadlay, P. F. Mutagenesis of a modular polyketide synthase enoylreductase domain reveals insights into catalysis and stereospecificity. ACS Chem. Biol. 5, 829-838 (2010).
    • (2010) ACS Chem. Biol. , vol.5 , pp. 829-838
    • Kwan, D.H.1    Leadlay, P.F.2
  • 57
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
    • Mosmann, T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods 65, 55-63 (1983).
    • (1983) J. Immunol. Methods , vol.65 , pp. 55-63
    • Mosmann, T.1
  • 59
    • 84855713144 scopus 로고    scopus 로고
    • Autoluminescent Mycobacterium tuberculosis for rapid, real-time, non-invasive assessment of drug and vaccine efficacy
    • Zhang, T., Li, S. Y. & Nuermberger, E. L. Autoluminescent Mycobacterium tuberculosis for rapid, real-time, non-invasive assessment of drug and vaccine efficacy. PLoS ONE 7, e29774 (2012).
    • (2012) PLoS ONE , vol.7 , pp. e29774
    • Zhang, T.1    Li, S.Y.2    Nuermberger, E.L.3


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