-
1
-
-
84923112133
-
-
Pharmaceutical Research and Manufacturers of America. Biopharmaceutical Research Industry Profile, Accessed December 1, 2014
-
Pharmaceutical Research and Manufacturers of America. Biopharmaceutical Research Industry Profile. 2014; Available from: http://www.phrma.org/sites/default/files/pdf/2014_PhRMA_PROFILE.pdf. Accessed December 1, 2014.
-
(2014)
-
-
-
2
-
-
77649234756
-
How to improve R&D productivity: The pharmaceutical industry’s grand challenge
-
Paul SM, Mytelka DS, Dunwiddie CT, et al. How to improve R&D productivity: the pharmaceutical industry’s grand challenge. Nat Rev Drug Discov. 2010;9(3):203–214.
-
(2010)
Nat Rev Drug Discov
, vol.9
, Issue.3
, pp. 203-214
-
-
Paul, S.M.1
Mytelka, D.S.2
Dunwiddie, C.T.3
-
3
-
-
84876002671
-
Natural products: A continuing source of novel drug leads
-
Cragg GM, Newman DJ. Natural products: a continuing source of novel drug leads. Biochim Biophys Acta. 2013;1830(6):3670–3695.
-
(2013)
Biochim Biophys Acta
, vol.1830
, Issue.6
, pp. 3670-3695
-
-
Cragg, G.M.1
Newman, D.J.2
-
4
-
-
77649305354
-
Natural products version 2.0: Connecting genes to molecules
-
Walsh CT, Fischbach MA. Natural products version 2.0: connecting genes to molecules. J Am Chem Soc. 2010;132(8):2469–2493.
-
(2010)
J am Chem Soc
, vol.132
, Issue.8
, pp. 2469-2493
-
-
Walsh, C.T.1
Fischbach, M.A.2
-
5
-
-
84896733954
-
Steps towards the synthetic biology of polyketide biosynthesis
-
Cummings M, Breitling R, Takano E. Steps towards the synthetic biology of polyketide biosynthesis. FEMS Microbiol Lett. 2014;351(2):116–125.
-
(2014)
FEMS Microbiol Lett
, vol.351
, Issue.2
, pp. 116-125
-
-
Cummings, M.1
Breitling, R.2
Takano, E.3
-
6
-
-
84859643086
-
Combinatorial biosynthesis of polyketides – a perspective
-
Wong FT, Khosla C. Combinatorial biosynthesis of polyketides – a perspective. Curr Opin Chem Biol. 2012;16(1–2):117–123.
-
(2012)
Curr Opin Chem Biol
, vol.16
, Issue.1-2
, pp. 117-123
-
-
Wong, F.T.1
Khosla, C.2
-
7
-
-
84865515585
-
Synthetic biological approaches to natural product biosynthesis
-
Winter JM, Tang Y. Synthetic biological approaches to natural product biosynthesis. Curr Opin Biotechnol. 2012;23(5):736–743.
-
(2012)
Curr Opin Biotechnol
, vol.23
, Issue.5
, pp. 736-743
-
-
Winter, J.M.1
Tang, Y.2
-
8
-
-
84863946395
-
The generation of “unnatural” products: Synthetic biology meets synthetic chemistry
-
Goss RJ, Shankar S, Fayad AA. The generation of “unnatural” products: synthetic biology meets synthetic chemistry. Nat Prod Rep. 2012;29(8):870–889.
-
(2012)
Nat Prod Rep
, vol.29
, Issue.8
, pp. 870-889
-
-
Goss, R.J.1
Shankar, S.2
Fayad, A.A.3
-
9
-
-
85027927172
-
Predicted Incorporation of non-native substrates by a polyketide synthase yields bioactive natural product derivatives
-
Bravo-Rodriguez K, Ismail-Ali AF, Klopries S, et al. Predicted Incorporation of non-native substrates by a polyketide synthase yields bioactive natural product derivatives. Chembiochem. 2014;15(13):1991–1997.
-
(2014)
Chembiochem
, vol.15
, Issue.13
, pp. 1991-1997
-
-
Bravo-Rodriguez, K.1
Ismail-Ali, A.F.2
Klopries, S.3
-
10
-
-
84878401236
-
Small molecule inhibition of the KRAS-PDEdelta interaction impairs oncogenic KRAS signalling
-
Zimmermann G, Papke B, Ismail S, et al. Small molecule inhibition of the KRAS-PDEdelta interaction impairs oncogenic KRAS signalling. Nature. 2013;497(7451):638–642.
-
(2013)
Nature
, vol.497
, Issue.7451
, pp. 638-642
-
-
Zimmermann, G.1
Papke, B.2
Ismail, S.3
-
11
-
-
84864275239
-
Precursor directed biosynthesis of an orthogonally functional erythromycin analogue: Selectivity in the ribosome macrolide binding pocket
-
Harvey CJ, Puglisi JD, Pande VS, Cane DE, Khosla C. Precursor directed biosynthesis of an orthogonally functional erythromycin analogue: selectivity in the ribosome macrolide binding pocket. J Am Chem Soc. 2012;134(29):12259–12265.
-
(2012)
J am Chem Soc
, vol.134
, Issue.29
, pp. 12259-12265
-
-
Harvey, C.J.1
Puglisi, J.D.2
Pande, V.S.3
Cane, D.E.4
Khosla, C.5
-
12
-
-
84859083398
-
Type III polyketide synthases in natural product biosynthesis
-
Yu D, Xu F, Zeng J, Zhan J. Type III polyketide synthases in natural product biosynthesis. IUBMB Life. 2012;64(4):285–295.
-
(2012)
IUBMB Life
, vol.64
, Issue.4
, pp. 285-295
-
-
Yu, D.1
Xu, F.2
Zeng, J.3
Zhan, J.4
-
13
-
-
79953855889
-
Cytotoxic tetramic acid derivative produced by a plant type-III polyketide synthase
-
Wakimoto T, Mori T, Morita H, Abe I. Cytotoxic tetramic acid derivative produced by a plant type-III polyketide synthase. J Am Chem Soc. 2011;133(13):4746–4749.
-
(2011)
J am Chem Soc
, vol.133
, Issue.13
, pp. 4746-4749
-
-
Wakimoto, T.1
Mori, T.2
Morita, H.3
Abe, I.4
-
14
-
-
33846781472
-
An acridone-producing novel multifunctional type III polyketide synthase from Huperzia serrata
-
Wanibuchi K, Zhang P, Abe T, et al. An acridone-producing novel multifunctional type III polyketide synthase from Huperzia serrata. FEBS J. 2007;274(4):1073–1082.
-
(2007)
FEBS J
, vol.274
, Issue.4
, pp. 1073-1082
-
-
Wanibuchi, K.1
Zhang, P.2
Abe, T.3
-
15
-
-
80051986672
-
Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase
-
Morita H, Yamashita M, Shi SP, et al. Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase. Proc Natl Acad Sci U S A. 2011;108(33):13504–13509.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, Issue.33
, pp. 13504-13509
-
-
Morita, H.1
Yamashita, M.2
Shi, S.P.3
-
16
-
-
84871826475
-
Structure and noncanonical chemistry of nonribosomal peptide biosynthetic machinery
-
Condurso HL, Bruner SD. Structure and noncanonical chemistry of nonribosomal peptide biosynthetic machinery. Nat Prod Rep. 2012;29(10):1099–1110.
-
(2012)
Nat Prod Rep
, vol.29
, Issue.10
, pp. 1099-1110
-
-
Condurso, H.L.1
Bruner, S.D.2
-
17
-
-
60349121247
-
New pacidamycin antibiotics through precursor-directed biosynthesis
-
Grüschow S, Rackham EJ, Elkins B, Newill PLA, Hill LM, Goss RJM. New pacidamycin antibiotics through precursor-directed biosynthesis. Chembiochem. 2009;10(2):355–360.
-
(2009)
Chembiochem
, vol.10
, Issue.2
, pp. 355-360
-
-
Grüschow, S.1
Rackham, E.J.2
Elkins, B.3
Newill, P.4
Hill, L.M.5
Goss, R.6
-
18
-
-
84905018416
-
NRPS substrate promiscuity leads to more potent antitubercular sansanmycin analogues
-
Xie Y, Cai Q, Ren H, et al. NRPS substrate promiscuity leads to more potent antitubercular sansanmycin analogues. J Nat Prod. 2014;77(7):1744–1748.
-
(2014)
J Nat Prod
, vol.77
, Issue.7
, pp. 1744-1748
-
-
Xie, Y.1
Cai, Q.2
Ren, H.3
-
19
-
-
77954578876
-
New pacidamycins biosynthetically: Probing N- and C-terminal substrate specificity
-
Ragab AE, Gruschow S, Rackham EJ, Goss RJ. New pacidamycins biosynthetically: probing N- and C-terminal substrate specificity. Org Biomol Chem. 2010;8(14):3128–3129.
-
(2010)
Org Biomol Chem
, vol.8
, Issue.14
, pp. 3128-3129
-
-
Ragab, A.E.1
Gruschow, S.2
Rackham, E.J.3
Goss, R.J.4
-
20
-
-
79953727021
-
Nine enzymes are required for assembly of the pacidamycin group of peptidyl nucleoside antibiotics
-
Zhang W, Ntai I, Bolla ML, et al. Nine enzymes are required for assembly of the pacidamycin group of peptidyl nucleoside antibiotics. J Am Chem Soc. 2011;133(14):5240–5243.
-
(2011)
J am Chem Soc
, vol.133
, Issue.14
, pp. 5240-5243
-
-
Zhang, W.1
Ntai, I.2
Bolla, M.L.3
-
21
-
-
84889036966
-
Precursor-directed biosynthesis of micacocidin derivatives with activity against Mycoplasma pneumoniae
-
Kreutzer MF, Kage H, Herrmann J, et al. Precursor-directed biosynthesis of micacocidin derivatives with activity against Mycoplasma pneumoniae. Org Biomol Chem. 2014;12(1):113–118.
-
(2014)
Org Biomol Chem
, vol.12
, Issue.1
, pp. 113-118
-
-
Kreutzer, M.F.1
Kage, H.2
Herrmann, J.3
-
22
-
-
80052240165
-
Production of anticancer polyenes through precursor-directed biosynthesis
-
Clark BR, O’Connor S, Fox D, Leroy J, Murphy CD. Production of anticancer polyenes through precursor-directed biosynthesis. Org Biomol Chem. 2011;9(18):6306–6311.
-
(2011)
Org Biomol Chem
, vol.9
, Issue.18
, pp. 6306-6311
-
-
Clark, B.R.1
O’Connor, S.2
Fox, D.3
Leroy, J.4
Murphy, C.D.5
-
23
-
-
65249180102
-
Evaluating indole-related derivatives as precursors in the directed biosynthesis of diazepinomicin analogues
-
Ratnayake AS, Janso JE, Feng X, Schlingmann G, Goljer I, Carter GT. Evaluating indole-related derivatives as precursors in the directed biosynthesis of diazepinomicin analogues. J Nat Prod. 2009;72(3):496–499.
-
(2009)
J Nat Prod
, vol.72
, Issue.3
, pp. 496-499
-
-
Ratnayake, A.S.1
Janso, J.E.2
Feng, X.3
Schlingmann, G.4
Goljer, I.5
Carter, G.T.6
-
24
-
-
84903436332
-
Structure of a modular polyketide synthase
-
Dutta S, Whicher JR, Hansen DA, et al. Structure of a modular polyketide synthase. Nature. 2014;510(7506):512–517.
-
(2014)
Nature
, vol.510
, Issue.7506
, pp. 512-517
-
-
Dutta, S.1
Whicher, J.R.2
Hansen, D.A.3
-
25
-
-
84903481589
-
Structural rearrangements of a polyketide synthase module during its catalytic cycle
-
Whicher JR, Dutta S, Hansen DA, et al. Structural rearrangements of a polyketide synthase module during its catalytic cycle. Nature. 2014;510(7506):560–564.
-
(2014)
Nature
, vol.510
, Issue.7506
, pp. 560-564
-
-
Whicher, J.R.1
Dutta, S.2
Hansen, D.A.3
-
26
-
-
0033515090
-
Multiple genetic modifications of the erythromycin polyketide synthase to produce a library of novel “unnatural” natural products
-
McDaniel R, Thamchaipenet A, Gustafsson C, Fu H, Betlach M, Ashley G. Multiple genetic modifications of the erythromycin polyketide synthase to produce a library of novel “unnatural” natural products. Proc Natl Acad Sci U S A. 1999;96(5):1846–1851.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, Issue.5
, pp. 1846-1851
-
-
McDaniel, R.1
Thamchaipenet, A.2
Gustafsson, C.3
Fu, H.4
Betlach, M.5
Ashley, G.6
-
27
-
-
29244459093
-
Natural products to drugs: Daptomycin and related lipopeptide antibiotics
-
Baltz RH, Miao V, Wrigley SK. Natural products to drugs: daptomycin and related lipopeptide antibiotics. Nat Prod Rep. 2005;22(6):717–741.
-
(2005)
Nat Prod Rep
, vol.22
, Issue.6
, pp. 717-741
-
-
Baltz, R.H.1
Miao, V.2
Wrigley, S.K.3
-
28
-
-
53449085206
-
Non-ribosomal peptide synthetase module fusions to produce derivatives of daptomycin in Streptomyces roseosporus
-
Doekel S, Coeffet-Le Gal MF, Gu JQ, Chu M, Baltz RH, Brian P. Non-ribosomal peptide synthetase module fusions to produce derivatives of daptomycin in Streptomyces roseosporus. Microbiology. 2008;154(Pt 9):2872–2880.
-
(2008)
Microbiology
, vol.154
, Issue.9
, pp. 2872-2880
-
-
Doekel, S.1
Coeffet-Le Gal, M.F.2
Gu, J.Q.3
Chu, M.4
Baltz, R.H.5
Brian, P.6
-
29
-
-
77950101233
-
Genetically engineered lipopeptide antibiotics related to A54145 and daptomycin with improved properties
-
Nguyen KT, He X, Alexander DC, et al. Genetically engineered lipopeptide antibiotics related to A54145 and daptomycin with improved properties. Antimicrob Agents Chemother. 2010;54(4):1404–1413.
-
(2010)
Antimicrob Agents Chemother
, vol.54
, Issue.4
, pp. 1404-1413
-
-
Nguyen, K.T.1
He, X.2
Alexander, D.C.3
-
30
-
-
30844455997
-
Combinatorial biosynthesis of lipopeptide antibiotics in Streptomyces roseosporus
-
Baltz RH, Brian P, Miao V, Wrigley SK. Combinatorial biosynthesis of lipopeptide antibiotics in Streptomyces roseosporus. J Ind Microbiol Biotechnol. 2006;33(2):66–74.
-
(2006)
J Ind Microbiol Biotechnol
, vol.33
, Issue.2
, pp. 66-74
-
-
Baltz, R.H.1
Brian, P.2
Miao, V.3
Wrigley, S.K.4
-
31
-
-
0034887171
-
Polyketide biosynthesis: A millennium review
-
Staunton J, Weissman KJ. Polyketide biosynthesis: a millennium review. Nat Prod Rep. 2001;18(4):380–416.
-
(2001)
Nat Prod Rep
, vol.18
, Issue.4
, pp. 380-416
-
-
Staunton, J.1
Weissman, K.J.2
-
32
-
-
78449290452
-
New insights into the formation of fungal aromatic polyketides
-
Crawford JM, Townsend CA. New insights into the formation of fungal aromatic polyketides. Nat Rev Microbiol. 2010;8(12):879–889.
-
(2010)
Nat Rev Microbiol
, vol.8
, Issue.12
, pp. 879-889
-
-
Crawford, J.M.1
Townsend, C.A.2
-
33
-
-
84864256859
-
Synthesis of (R)-mellein by a partially reducing iterative polyketide synthase
-
Sun H, Ho CL, Ding F, Soehano I, Liu XW, Liang ZX. Synthesis of (R)-mellein by a partially reducing iterative polyketide synthase. J Am Chem Soc. 2012;134(29):11924–11927.
-
(2012)
J am Chem Soc
, vol.134
, Issue.29
, pp. 11924-11927
-
-
Sun, H.1
Ho, C.L.2
Ding, F.3
Soehano, I.4
Liu, X.W.5
Liang, Z.X.6
-
34
-
-
80054760185
-
Rational domain swaps decipher programming in fungal highly reducing polyketide synthases and resurrect an extinct metabolite
-
Fisch KM, Bakeer W, Yakasai AA, et al. Rational domain swaps decipher programming in fungal highly reducing polyketide synthases and resurrect an extinct metabolite. J Am Chem Soc. 2011;133(41):16635–16641.
-
(2011)
J am Chem Soc
, vol.133
, Issue.41
, pp. 16635-16641
-
-
Fisch, K.M.1
Bakeer, W.2
Yakasai, A.A.3
-
35
-
-
80052078373
-
Engineering of an “unnatural” natural product by swapping polyketide synthase domains in Aspergillus nidulans
-
Liu T, Chiang YM, Somoza AD, Oakley BR, Wang CC. Engineering of an “unnatural” natural product by swapping polyketide synthase domains in Aspergillus nidulans. J Am Chem Soc. 2011;133(34):13314–13316.
-
(2011)
J am Chem Soc
, vol.133
, Issue.34
, pp. 13314-13316
-
-
Liu, T.1
Chiang, Y.M.2
Somoza, A.D.3
Oakley, B.R.4
Wang, C.C.5
-
36
-
-
84896929356
-
Rational domain swaps reveal insights about chain length control by ketosynthase domains in fungal nonreducing polyketide synthases
-
Liu T, Sanchez JF, Chiang YM, Oakley BR, Wang CC. Rational domain swaps reveal insights about chain length control by ketosynthase domains in fungal nonreducing polyketide synthases. Org Lett. 2014;16(6):1676–1679.
-
(2014)
Org Lett
, vol.16
, Issue.6
, pp. 1676-1679
-
-
Liu, T.1
Sanchez, J.F.2
Chiang, Y.M.3
Oakley, B.R.4
Wang, C.C.5
-
37
-
-
84873941080
-
Engineering fungal nonreducing polyketide synthase by heterologous expression and domain swapping
-
Yeh HH, Chang SL, Chiang YM, et al. Engineering fungal nonreducing polyketide synthase by heterologous expression and domain swapping. Org Lett. 2013;15(4):756–759.
-
(2013)
Org Lett
, vol.15
, Issue.4
, pp. 756-759
-
-
Yeh, H.H.1
Chang, S.L.2
Chiang, Y.M.3
-
38
-
-
84880809096
-
Thioesterase domains of fungal nonreducing polyketide synthases act as decision gates during combinatorial biosynthesis
-
Xu Y, Zhou T, Zhang S, Xuan LJ, Zhan J, Molnar I. Thioesterase domains of fungal nonreducing polyketide synthases act as decision gates during combinatorial biosynthesis. J Am Chem Soc. 2013;135(29):10783–10791.
-
(2013)
J am Chem Soc
, vol.135
, Issue.29
, pp. 10783-10791
-
-
Xu, Y.1
Zhou, T.2
Zhang, S.3
Xuan, L.J.4
Zhan, J.5
Molnar, I.6
-
39
-
-
84869169169
-
Navigating the fungal polyketide chemical space: From genes to molecules
-
Chooi YH, Tang Y. Navigating the fungal polyketide chemical space: from genes to molecules. J Org Chem. 2012;77(22):9933–9953.
-
(2012)
J Org Chem
, vol.77
, Issue.22
, pp. 9933-9953
-
-
Chooi, Y.H.1
Tang, Y.2
-
40
-
-
84874805716
-
Characterization of the biosynthetic genes for 10,11-dehydrocurvularin, a heat shock response-modulating anticancer fungal polyketide from Aspergillus terreus
-
Xu Y, Espinosa-Artiles P, Schubert V, et al. Characterization of the biosynthetic genes for 10,11-dehydrocurvularin, a heat shock response-modulating anticancer fungal polyketide from Aspergillus terreus. Appl Environ Microbiol. 2013;79(6):2038–2047.
-
(2013)
Appl Environ Microbiol
, vol.79
, Issue.6
, pp. 2038-2047
-
-
Xu, Y.1
Espinosa-Artiles, P.2
Schubert, V.3
-
41
-
-
84906672709
-
Diversity-oriented combinatorial biosynthesis of benzenediol lactone scaffolds by subunit shuffling of fungal polyketide synthases
-
Xu Y, Zhou T, Zhang S, et al. Diversity-oriented combinatorial biosynthesis of benzenediol lactone scaffolds by subunit shuffling of fungal polyketide synthases. Proc Natl Acad Sci U S A. 2014;111(34):12354–12359.
-
(2014)
Proc Natl Acad Sci U S A
, vol.111
, Issue.34
, pp. 12354-12359
-
-
Xu, Y.1
Zhou, T.2
Zhang, S.3
-
42
-
-
84867512666
-
Minimally invasive mutagenesis gives rise to a biosynthetic polyketide library
-
Kushnir S, Sundermann U, Yahiaoui S, Brockmeyer A, Janning P, Schulz F. Minimally invasive mutagenesis gives rise to a biosynthetic polyketide library. Angew Chem Int Ed Engl. 2012;51(42):10664–10669.
-
(2012)
Angew Chem Int Ed Engl
, vol.51
, Issue.42
, pp. 10664-10669
-
-
Kushnir, S.1
Sundermann, U.2
Yahiaoui, S.3
Brockmeyer, A.4
Janning, P.5
Schulz, F.6
-
43
-
-
84883484875
-
Expanding the fluorine chemistry of living systems using engineered polyketide synthase pathways
-
Walker MC, Thuronyi BW, Charkoudian LK, Lowry B, Khosla C, Chang MC. Expanding the fluorine chemistry of living systems using engineered polyketide synthase pathways. Science. 2013;341(6150):1089–1094.
-
(2013)
Science
, vol.341
, Issue.6150
, pp. 1089-1094
-
-
Walker, M.C.1
Thuronyi, B.W.2
Charkoudian, L.K.3
Lowry, B.4
Khosla, C.5
Chang, M.C.6
-
44
-
-
84897584974
-
Fluorine in pharmaceutical industry: Fluorine-containing drugs introduced to the market in the last decade (2001–2011)
-
Wang J, Sanchez-Rosello M, Acena JL, et al. Fluorine in pharmaceutical industry: fluorine-containing drugs introduced to the market in the last decade (2001–2011). Chem Rev. 2014;114(4):2432–2506.
-
(2014)
Chem Rev
, vol.114
, Issue.4
, pp. 2432-2506
-
-
Wang, J.1
Sanchez-Rosello, M.2
Acena, J.L.3
-
45
-
-
60849085462
-
Enzymatic formation of unnatural novel chalcone, stilbene, and benzophenone scaffolds by plant type III polyketide synthase
-
Shi SP, Wanibuchi K, Morita H, Endo K, Noguchi H, Abe I. Enzymatic formation of unnatural novel chalcone, stilbene, and benzophenone scaffolds by plant type III polyketide synthase. Org Lett. 2009;11(3):551–554.
-
(2009)
Org Lett
, vol.11
, Issue.3
, pp. 551-554
-
-
Shi, S.P.1
Wanibuchi, K.2
Morita, H.3
Endo, K.4
Noguchi, H.5
Abe, I.6
-
46
-
-
78649358322
-
Engineered biosynthesis of plant polyketides: Structure-based and precursor-directed approach
-
Abe I. Engineered biosynthesis of plant polyketides: structure-based and precursor-directed approach. Top Curr Chem. 2010;297:45–66.
-
(2010)
Top Curr Chem
, vol.297
, pp. 45-66
-
-
Abe, I.1
-
47
-
-
78650544821
-
Structural basis for the one-pot formation of the diarylheptanoid scaffold by curcuminoid synthase from Oryza sativa
-
Morita H, Wanibuchi K, Nii H, Kato R, Sugio S, Abe I. Structural basis for the one-pot formation of the diarylheptanoid scaffold by curcuminoid synthase from Oryza sativa. Proc Natl Acad Sci U S A. 2010;107(46):19778–19783.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, Issue.46
, pp. 19778-19783
-
-
Morita, H.1
Wanibuchi, K.2
Nii, H.3
Kato, R.4
Sugio, S.5
Abe, I.6
-
48
-
-
84863822575
-
Introduction of a non-natural amino acid into a nonribosomal peptide antibiotic by modification of adenylation domain specificity
-
Thirlway J, Lewis R, Nunns L, et al. Introduction of a non-natural amino acid into a nonribosomal peptide antibiotic by modification of adenylation domain specificity. Angew Chem Int Ed. 2012;51(29):7181–7184.
-
(2012)
Angew Chem Int
, vol.51
, Issue.29
, pp. 7181-7184
-
-
Thirlway, J.1
Lewis, R.2
Nunns, L.3
-
49
-
-
34547547069
-
Directed evolution can rapidly improve the activity of chimeric assembly-line enzymes
-
Fischbach MA, Lai JR, Roche ED, Walsh CT, Liu DR. Directed evolution can rapidly improve the activity of chimeric assembly-line enzymes. Proc Natl Acad Sci U S A. 2007;104(29):11951–11956.
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, Issue.29
, pp. 11951-11956
-
-
Fischbach, M.A.1
Lai, J.R.2
Roche, E.D.3
Walsh, C.T.4
Liu, D.R.5
-
50
-
-
79957450871
-
Directed evolution of the nonribosomal peptide synthetase AdmK generates new andrimid derivatives in vivo
-
Evans BS, Chen Y, Metcalf WW, Zhao H, Kelleher NL. Directed evolution of the nonribosomal peptide synthetase AdmK generates new andrimid derivatives in vivo. Chem Biol. 2011;18(5):601–607.
-
(2011)
Chem Biol
, vol.18
, Issue.5
, pp. 601-607
-
-
Evans, B.S.1
Chen, Y.2
Metcalf, W.W.3
Zhao, H.4
Kelleher, N.L.5
-
51
-
-
84872934815
-
Engineering the substrate specificity of the DhbE adenylation domain by yeast cell surface display
-
Zhang K, Nelson KM, Bhuripanyo K, et al. Engineering the substrate specificity of the DhbE adenylation domain by yeast cell surface display. Chem Biol. 2013;20(1):92–101.
-
(2013)
Chem Biol
, vol.20
, Issue.1
, pp. 92-101
-
-
Zhang, K.1
Nelson, K.M.2
Bhuripanyo, K.3
-
52
-
-
0021844476
-
Production of ‘hybrid’antibiotics by genetic engineering
-
Hopwood DA, Malpartida F, Kieser H, et al. Production of ‘hybrid’antibiotics by genetic engineering. Nature. 1985;314:642–644.
-
(1985)
Nature
, vol.314
, pp. 642-644
-
-
Hopwood, D.A.1
Malpartida, F.2
Kieser, H.3
-
53
-
-
84877983328
-
Combinatorial biosynthesis of legume natural and rare triterpenoids in engineered yeast
-
Seki H, Sawai S, Ohyama K, et al. Combinatorial biosynthesis of legume natural and rare triterpenoids in engineered yeast. Plant Cell Physiol. 2013;54(5):740–749.
-
(2013)
Plant Cell Physiol
, vol.54
, Issue.5
, pp. 740-749
-
-
Seki, H.1
Sawai, S.2
Ohyama, K.3
-
54
-
-
84855180697
-
Triterpene functional genomics in licorice for identification of CYP72A154 involved in the biosynthesis of glycyrrhizin
-
Seki H, Sawai S, Ohyama K, et al. Triterpene functional genomics in licorice for identification of CYP72A154 involved in the biosynthesis of glycyrrhizin. Plant Cell. 2011;23(11):4112–4123.
-
(2011)
Plant Cell
, vol.23
, Issue.11
, pp. 4112-4123
-
-
Seki, H.1
Sawai, S.2
Ohyama, K.3
-
55
-
-
84893351504
-
Combinatorial biosynthesis of sapogenins and saponins in Saccharomyces cerevisiae using a C-16α hydroxylase from Bupleurum falcatum
-
Moses T, Pollier J, Almagro L, et al. Combinatorial biosynthesis of sapogenins and saponins in Saccharomyces cerevisiae using a C-16α hydroxylase from Bupleurum falcatum. Proc Natl Acad Sci U S A. 2014;111(4):1634–1639.
-
(2014)
Proc Natl Acad Sci U S A
, vol.111
, Issue.4
, pp. 1634-1639
-
-
Moses, T.1
Pollier, J.2
Almagro, L.3
-
56
-
-
84923087807
-
The role of genetic engineering in natural product-based anticancer drug discovery
-
Koehn FE, editor, New York, NY: SpringerScience+BusinessMedia
-
Unsin CE-M, Rajski SR, Shen B. The role of genetic engineering in natural product-based anticancer drug discovery. In: Koehn FE, editor. Natural Products and Cancer Drug Discovery. New York, NY: SpringerScience+BusinessMedia; 2013:175–191.
-
(2013)
Natural Products and Cancer Drug Discovery
, pp. 175-191
-
-
Unsin, C.-M.1
Rajski, S.R.2
Shen, B.3
-
57
-
-
84923100134
-
Harnessing sugar biosynthesis and glycosylation to redesign natural products and to increase structural diversity
-
In: Osbourn A Goss RJ, Carter GT, editors, Hoboken, NJ: John Wiley & Sons
-
Olano C, Méndez C, Salas JA. Harnessing sugar biosynthesis and glycosylation to redesign natural products and to increase structural diversity. In: Osbourn A Goss RJ, Carter GT, editors. Natural Products: Discourse, Diversity, and Design. Hoboken, NJ: John Wiley & Sons; 2014:317–340.
-
(2014)
Natural Products: Discourse, Diversity, and Design
, pp. 317-340
-
-
Olano, C.1
Méndez, C.2
Salas, J.A.3
-
58
-
-
84863109265
-
A novel mithramycin analogue with high antitumor activity and less toxicity generated by combinatorial biosynthesis
-
Núñez LE, Nybo SE, González-Sabín J, et al. A novel mithramycin analogue with high antitumor activity and less toxicity generated by combinatorial biosynthesis. J Med Chem. 2012;55(12):5813–5825.
-
(2012)
J Med Chem
, vol.55
, Issue.12
, pp. 5813-5825
-
-
Núñez, L.E.1
Nybo, S.E.2
González-Sabín, J.3
-
59
-
-
79551474367
-
Engineered biosynthesis of gilvocarcin analogues with altered deoxyhexopyranose moieties
-
Shepherd MD, Liu T, Méndez C, Salas JA, Rohr J. Engineered biosynthesis of gilvocarcin analogues with altered deoxyhexopyranose moieties. Appl Environ Microbiol. 2011;77(2):435–441.
-
(2011)
Appl Environ Microbiol
, vol.77
, Issue.2
, pp. 435-441
-
-
Shepherd, M.D.1
Liu, T.2
Méndez, C.3
Salas, J.A.4
Rohr, J.5
-
60
-
-
79961051540
-
Development of a Streptomyces venezuelae-based combinatorial biosynthetic system for the production of glycosylated derivatives of doxorubicin and its biosynthetic intermediates
-
Han AR, Park JW, Lee MK, et al. Development of a Streptomyces venezuelae-based combinatorial biosynthetic system for the production of glycosylated derivatives of doxorubicin and its biosynthetic intermediates. Appl Environ Microbiol. 2011;77(14):4912–4923.
-
(2011)
Appl Environ Microbiol
, vol.77
, Issue.14
, pp. 4912-4923
-
-
Han, A.R.1
Park, J.W.2
Lee, M.K.3
-
61
-
-
34648822399
-
Bioconversion of 12-, 14-, and 16-membered ring aglycones to glycosylated macrolides in an engineered strain of Streptomyces venezuelae
-
Jung WS, Han AR, Hong JSJ, et al. Bioconversion of 12-, 14-, and 16-membered ring aglycones to glycosylated macrolides in an engineered strain of Streptomyces venezuelae. Appl Microbiol Biotechnol. 2007;76(6):1373–1381.
-
(2007)
Appl Microbiol Biotechnol
, vol.76
, Issue.6
, pp. 1373-1381
-
-
Jung, W.S.1
Han, A.R.2
Hong, J.3
-
62
-
-
33748999758
-
Heterologous expression of tylosin polyketide synthase and production of a hybrid bioactive macrolide in Streptomyces venezuelae
-
Jung WS, Lee SK, Hong JSJ, et al. Heterologous expression of tylosin polyketide synthase and production of a hybrid bioactive macrolide in Streptomyces venezuelae. Appl Microbiol Biotechnol. 2006;72(4):763–769.
-
(2006)
Appl Microbiol Biotechnol
, vol.72
, Issue.4
, pp. 763-769
-
-
Jung, W.S.1
Lee, S.K.2
Hong, J.3
-
63
-
-
84856380205
-
Engineered biosynthesis of glycosylated derivatives of narbomycin and evaluation of their antibacterial activities
-
Han AR, Shinde PB, Park JW, et al. Engineered biosynthesis of glycosylated derivatives of narbomycin and evaluation of their antibacterial activities. Appl Microbiol Biotechnol. 2012;93(3):1147–1156.
-
(2012)
Appl Microbiol Biotechnol
, vol.93
, Issue.3
, pp. 1147-1156
-
-
Han, A.R.1
Shinde, P.B.2
Park, J.W.3
-
64
-
-
84885843967
-
Combinatorial biosynthesis and antibacterial evaluation of glycosylated derivatives of 12-membered macrolide antibiotic YC-17
-
Shinde PB, Han AR, Cho J, et al. Combinatorial biosynthesis and antibacterial evaluation of glycosylated derivatives of 12-membered macrolide antibiotic YC-17. J Biotechnol. 2013;168(2):142–148.
-
(2013)
J Biotechnol
, vol.168
, Issue.2
, pp. 142-148
-
-
Shinde, P.B.1
Han, A.R.2
Cho, J.3
-
65
-
-
33745438002
-
Fabulous fluorine
-
Thayer AM. Fabulous fluorine. Chem Eng News. 2006;84(23):15–24.
-
(2006)
Chem Eng News
, vol.84
, Issue.23
, pp. 15-24
-
-
Thayer, A.M.1
-
66
-
-
77950455094
-
Engineering fluorometabolite production: Fluorinase expression in Salinispora tropica yields fluorosalinosporamide
-
Eustáquio AS, O’Hagan D, Moore BS. Engineering fluorometabolite production: fluorinase expression in Salinispora tropica yields fluorosalinosporamide. J Nat Prod. 2010;73(3):378–382.
-
(2010)
J Nat Prod
, vol.73
, Issue.3
, pp. 378-382
-
-
Eustáquio, A.S.1
O’Hagan, D.2
Moore, B.S.3
-
67
-
-
78549294465
-
Integrating carbon-halogen bond formation into medicinal plant metabolism
-
Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. 2010;468(7322):461–464.
-
(2010)
Nature
, vol.468
, Issue.7322
, pp. 461-464
-
-
Runguphan, W.1
Qu, X.2
O’Connor, S.E.3
-
68
-
-
84906672709
-
Diversity-oriented combinatorial biosynthesis of benzenediol lactone scaffolds by subunit shuffling of fungal polyketide synthases
-
Xu Y, Zhou T, Zhang S, et al. Diversity-oriented combinatorial biosynthesis of benzenediol lactone scaffolds by subunit shuffling of fungal polyketide synthases. Proc Natl Acad Sci U S A. 2014;111(34):12354–12359.
-
(2014)
Proc Natl Acad Sci U S A
, vol.111
, Issue.34
, pp. 12354-12359
-
-
Xu, Y.1
Zhou, T.2
Zhang, S.3
-
69
-
-
84902430164
-
Chirality and combinatorial libraries for drug discovery, an overview
-
Carreira EM, Yamamoto H, editors, Amsterdam, Netherlands: Elsevier
-
Mignani S, Patek M. Chirality and combinatorial libraries for drug discovery, an overview. In: Carreira EM, Yamamoto H, editors. Comprehensive Chirality. Amsterdam, Netherlands: Elsevier; 2012:217–245.
-
(2012)
Comprehensive Chirality
, pp. 217-245
-
-
Mignani, S.1
Patek, M.2
-
70
-
-
79959424209
-
Metabolic engineering for the production of natural products
-
Pickens LB, Tang Y, Chooi YH. Metabolic engineering for the production of natural products. Annu Rev Chem Biomol Eng. 2011;2:211–236.
-
(2011)
Annu Rev Chem Biomol Eng
, vol.2
, pp. 211-236
-
-
Pickens, L.B.1
Tang, Y.2
Chooi, Y.H.3
-
71
-
-
84887789916
-
Balanced globin protein expression and heme biosynthesis improve production of human hemoglobin in Saccharomyces cerevisiae
-
Liu L, Martínez JL, Liu Z, Petranovic D, Nielsen J. Balanced globin protein expression and heme biosynthesis improve production of human hemoglobin in Saccharomyces cerevisiae. Met Eng. 2014;21:9–16.
-
(2014)
Met Eng
, vol.21
, pp. 9-16
-
-
Liu, L.1
Martínez, J.L.2
Liu, Z.3
Petranovic, D.4
Nielsen, J.5
-
72
-
-
79952642503
-
Rapid characterization and engineering of natural product biosynthetic pathways via DNA assembler
-
Shao Z, Luo Y, Zhao H. Rapid characterization and engineering of natural product biosynthetic pathways via DNA assembler. Mol BioSyst. 2011;7(4):1056–1059.
-
(2011)
Mol Biosyst
, vol.7
, Issue.4
, pp. 1056-1059
-
-
Shao, Z.1
Luo, Y.2
Zhao, H.3
-
73
-
-
84893493312
-
DNA assembly techniques for next-generation combinatorial biosynthesis of natural products
-
Cobb RE, Ning JC, Zhao H. DNA assembly techniques for next-generation combinatorial biosynthesis of natural products. J Ind Microbiol Biotechnol. 2014;41(2):469–477.
-
(2014)
J Ind Microbiol Biotechnol
, vol.41
, Issue.2
, pp. 469-477
-
-
Cobb, R.E.1
Ning, J.C.2
Zhao, H.3
-
74
-
-
84937816186
-
Recent advances in DNA assembly technologies
-
Chao R, Yuan Y, Zhao H. Recent advances in DNA assembly technologies. FEMS Yeast Res. 2014. DOI: 10.1111/1567–1364.12171.
-
(2014)
FEMS Yeast Res
-
-
Chao, R.1
Yuan, Y.2
Zhao, H.3
-
75
-
-
84860741240
-
Engineering the third wave of biocatalysis
-
Bornscheuer U, Huisman G, Kazlauskas R, Lutz S, Moore J, Robins K. Engineering the third wave of biocatalysis. Nature. 2012;485(7397):185–194.
-
(2012)
Nature
, vol.485
, Issue.7397
, pp. 185-194
-
-
Bornscheuer, U.1
Huisman, G.2
Kazlauskas, R.3
Lutz, S.4
Moore, J.5
Robins, K.6
-
76
-
-
84893020696
-
High-throughput screening for industrial enzyme production hosts by droplet microfluidics
-
Sjostrom SL, Bai Y, Huang M, et al. High-throughput screening for industrial enzyme production hosts by droplet microfluidics. Lab Chip. 2014;14(4):806–813.
-
(2014)
Lab Chip
, vol.14
, Issue.4
, pp. 806-813
-
-
Sjostrom, S.L.1
Bai, Y.2
Huang, M.3
-
77
-
-
84891421517
-
Computational tools for designing and engineering enzymes
-
Damborsky J, Brezovsky J. Computational tools for designing and engineering enzymes. Curr Opin Chem Biol. 2014;19(0):8–16.
-
(2014)
Curr Opin Chem Biol
, vol.19
, Issue.0
, pp. 8-16
-
-
Damborsky, J.1
Brezovsky, J.2
-
79
-
-
58149234737
-
Real-time DNA sequencing from single polymerase molecules
-
Eid J, Fehr A, Gray J, et al. Real-time DNA sequencing from single polymerase molecules. Science. 2009;323(5910):133–138.
-
(2009)
Science
, vol.323
, Issue.5910
, pp. 133-138
-
-
Eid, J.1
Fehr, A.2
Gray, J.3
-
80
-
-
72849144434
-
Sequencing technologies – the next generation
-
Metzker ML. Sequencing technologies – the next generation. Nat Rev Genet. 2009;11(1):31–46.
-
(2009)
Nat Rev Genet
, vol.11
, Issue.1
, pp. 31-46
-
-
Metzker, M.L.1
-
81
-
-
84905917097
-
Improved production of a heterologous amylase in Saccharomyces cerevisiae by inverse metabolic engineering
-
Liu Z, Liu L, Österlund T, et al. Improved production of a heterologous amylase in Saccharomyces cerevisiae by inverse metabolic engineering. Appl Environ Microbiol. 2014;80(17):5542–5550.
-
(2014)
Appl Environ Microbiol
, vol.80
, Issue.17
, pp. 5542-5550
-
-
Liu, Z.1
Liu, L.2
Österlund, T.3
-
82
-
-
77956493932
-
Drug discovery from uncultivable microorganisms
-
Singh BK, Macdonald CA. Drug discovery from uncultivable microorganisms. Drug Discov Today. 2010;15(17–18):792–799.
-
(2010)
Drug Discov Today
, vol.15
, Issue.17-18
, pp. 792-799
-
-
Singh, B.K.1
Macdonald, C.A.2
-
83
-
-
79951848091
-
Molecular insights on the biosynthesis of antitumour compounds by actinomycetes
-
Olano C, Méndez C, Salas JA. Molecular insights on the biosynthesis of antitumour compounds by actinomycetes. Microb Biotechnol. 2011;4(2):144–164.
-
(2011)
Microb Biotechnol
, vol.4
, Issue.2
, pp. 144-164
-
-
Olano, C.1
Méndez, C.2
Salas, J.A.3
-
84
-
-
59349103269
-
Jasmonate-inducible gene: What does it mean?
-
Pauwels L, Inzé D, Goossens A. Jasmonate-inducible gene: what does it mean? Trends Plant Sci. 2009;14(2):87–91.
-
(2009)
Trends Plant Sci
, vol.14
, Issue.2
, pp. 87-91
-
-
Pauwels, L.1
Inzé, D.2
Goossens, A.3
|