-
1
-
-
0035843136
-
Combinatorial and computational challenges for biocatalyst design
-
Arnold F.H. Combinatorial and computational challenges for biocatalyst design. Nature 409 (2001) 253-257
-
(2001)
Nature
, vol.409
, pp. 253-257
-
-
Arnold, F.H.1
-
3
-
-
71149102452
-
-
Berg, V.A., Hans, M., and Steekstra, H. (2009). Method for the production of simvastatin. WO2007147801 (A1).
-
Berg, V.A., Hans, M., and Steekstra, H. (2009). Method for the production of simvastatin. WO2007147801 (A1).
-
-
-
-
4
-
-
0028816556
-
Direct random mutagenesis of gene-sized DNA fragments using polymerase chain-reaction
-
Fromant M., Blanquet S., and Plateau P. Direct random mutagenesis of gene-sized DNA fragments using polymerase chain-reaction. Anal. Biochem. 224 (1995) 347-353
-
(1995)
Anal. Biochem.
, vol.224
, pp. 347-353
-
-
Fromant, M.1
Blanquet, S.2
Plateau, P.3
-
5
-
-
0033153557
-
Of barn owls and bankers: a lush variety of alpha/beta hydrolases
-
Heikinheimo P., Goldman A., Jeffries C., and Ollis D.L. Of barn owls and bankers: a lush variety of alpha/beta hydrolases. Structure 7 (1999) R141-R146
-
(1999)
Structure
, vol.7
-
-
Heikinheimo, P.1
Goldman, A.2
Jeffries, C.3
Ollis, D.L.4
-
6
-
-
0022486908
-
3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 4. side-chain ester derivatives of mevinolin
-
Hoffman W.F., Alberts A.W., Anderson P.S., Chen J.S., Smith R.L., and Willard A.K. 3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 4. side-chain ester derivatives of mevinolin. J. Med. Chem. 29 (1986) 849-852
-
(1986)
J. Med. Chem.
, vol.29
, pp. 849-852
-
-
Hoffman, W.F.1
Alberts, A.W.2
Anderson, P.S.3
Chen, J.S.4
Smith, R.L.5
Willard, A.K.6
-
7
-
-
21544473154
-
Directed evolution of D-sialic acid aldolase to L-3-deoxy-manno-2-octulosonic acid (L-KDO) aldolase
-
Hsu C.C., Hong Z.Y., Wada M., Franke D., and Wong C.H. Directed evolution of D-sialic acid aldolase to L-3-deoxy-manno-2-octulosonic acid (L-KDO) aldolase. Proc. Natl. Acad. Sci. USA 102 (2005) 9122-9126
-
(2005)
Proc. Natl. Acad. Sci. USA
, vol.102
, pp. 9122-9126
-
-
Hsu, C.C.1
Hong, Z.Y.2
Wada, M.3
Franke, D.4
Wong, C.H.5
-
8
-
-
0035843962
-
Structural mechanism for statin inhibition of HMG-CoA reductase
-
Istvan E.S., and Deisenhofer J. Structural mechanism for statin inhibition of HMG-CoA reductase. Science 292 (2001) 1160-1164
-
(2001)
Science
, vol.292
, pp. 1160-1164
-
-
Istvan, E.S.1
Deisenhofer, J.2
-
9
-
-
0033591447
-
Modulation of polyketide synthase activity by accessory proteins during lovastatin biosynthesis
-
Kennedy J., Auclair K., Kendrew S.G., Park C., Vederas J.C., and Hutchinson C.R. Modulation of polyketide synthase activity by accessory proteins during lovastatin biosynthesis. Science 284 (1999) 1368-1372
-
(1999)
Science
, vol.284
, pp. 1368-1372
-
-
Kennedy, J.1
Auclair, K.2
Kendrew, S.G.3
Park, C.4
Vederas, J.C.5
Hutchinson, C.R.6
-
10
-
-
0033962763
-
A rapid technique for screening of lovastatin-producing strains of Aspergillus terreus by agar plug and Neurospora crassa bioassay
-
Kumar M.S., Kumar P.M., Sarnaik H.M., and Sadhukhan A.K. A rapid technique for screening of lovastatin-producing strains of Aspergillus terreus by agar plug and Neurospora crassa bioassay. J. Microbiol. Methods 40 (2000) 99-104
-
(2000)
J. Microbiol. Methods
, vol.40
, pp. 99-104
-
-
Kumar, M.S.1
Kumar, P.M.2
Sarnaik, H.M.3
Sadhukhan, A.K.4
-
11
-
-
33646086963
-
Profiling a taxol pathway 10 beta-acetyltransferase: Assessment of the specificity and the production of baccatin III by in vivo acetylation in E. coli
-
Loncaric C., Merriweather E., and Walker K.D. Profiling a taxol pathway 10 beta-acetyltransferase: Assessment of the specificity and the production of baccatin III by in vivo acetylation in E. coli. Chem. Biol. 13 (2006) 309-317
-
(2006)
Chem. Biol.
, vol.13
, pp. 309-317
-
-
Loncaric, C.1
Merriweather, E.2
Walker, K.D.3
-
12
-
-
71149116978
-
-
Morgan, B., Burk, M., Levin, M., Zhu, Z., Chaplin, J., Kustedjo, K., Huang, Z., and Greenberg, W. (2006). Methods for making simvastatin and intermediates. WO2005040107 (A2).
-
Morgan, B., Burk, M., Levin, M., Zhu, Z., Chaplin, J., Kustedjo, K., Huang, Z., and Greenberg, W. (2006). Methods for making simvastatin and intermediates. WO2005040107 (A2).
-
-
-
-
13
-
-
0032784276
-
Alpha/beta hydrolase fold enzymes: the family keeps growing
-
Nardini M., and Dijkstra B.W. Alpha/beta hydrolase fold enzymes: the family keeps growing. Curr. Opin. Struct. Biol. 9 (1999) 732-737
-
(1999)
Curr. Opin. Struct. Biol.
, vol.9
, pp. 732-737
-
-
Nardini, M.1
Dijkstra, B.W.2
-
14
-
-
39149099787
-
Halogenation strategies in natural product biosynthesis
-
Neumann C.S., Fujimori D.G., and Walsh C.T. Halogenation strategies in natural product biosynthesis. Chem. Biol. 15 (2008) 99-109
-
(2008)
Chem. Biol.
, vol.15
, pp. 99-109
-
-
Neumann, C.S.1
Fujimori, D.G.2
Walsh, C.T.3
-
15
-
-
0025022490
-
Refined crystal-structure of beta-lactamase from citrobacter-freundii Indicates a mechanism for beta-lactam hydrolysis
-
Oefner C., Darcy A., Daly J.J., Gubernator K., Charnas R.L., Heinze I., Hubschwerlen C., and Winkler F.K. Refined crystal-structure of beta-lactamase from citrobacter-freundii Indicates a mechanism for beta-lactam hydrolysis. Nature 343 (1990) 284-288
-
(1990)
Nature
, vol.343
, pp. 284-288
-
-
Oefner, C.1
Darcy, A.2
Daly, J.J.3
Gubernator, K.4
Charnas, R.L.5
Heinze, I.6
Hubschwerlen, C.7
Winkler, F.K.8
-
16
-
-
0033593453
-
Redesigning the substrate specificity of an enzyme by cumulative effects of the mutations of non-active site residues
-
Oue S., Okamoto A., Yano T., and Kagamiyama H. Redesigning the substrate specificity of an enzyme by cumulative effects of the mutations of non-active site residues. J. Biol. Chem. 274 (1999) 2344-2349
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 2344-2349
-
-
Oue, S.1
Okamoto, A.2
Yano, T.3
Kagamiyama, H.4
-
17
-
-
0035954552
-
A novel esterase from Burkholderia gladioli which shows high deacetylation activity on cephalosporins is related to beta-lactamases and DD-peptidases
-
Petersen E.I., Valinger G., Solkner B., Stubenrauch G., and Schwab H. A novel esterase from Burkholderia gladioli which shows high deacetylation activity on cephalosporins is related to beta-lactamases and DD-peptidases. J. Biotechnol. 89 (2001) 11-25
-
(2001)
J. Biotechnol.
, vol.89
, pp. 11-25
-
-
Petersen, E.I.1
Valinger, G.2
Solkner, B.3
Stubenrauch, G.4
Schwab, H.5
-
18
-
-
0036774667
-
Modification of post-PKS tailoring steps through combinatorial biosynthesis
-
Rix U., Fischer C., Remsing L.L., and Rohr J. Modification of post-PKS tailoring steps through combinatorial biosynthesis. Nat. Prod. Rep. 19 (2002) 542-580
-
(2002)
Nat. Prod. Rep.
, vol.19
, pp. 542-580
-
-
Rix, U.1
Fischer, C.2
Remsing, L.L.3
Rohr, J.4
-
19
-
-
36448996957
-
Computational design of the Fyn SH3 domain with increased stability through optimization of surface charge charge interactions
-
Schweiker K.L., Zarrine-Afsar A., Davidson A.R., and Makhatadze G.I. Computational design of the Fyn SH3 domain with increased stability through optimization of surface charge charge interactions. Protein Sci. 16 (2007) 2694-2702
-
(2007)
Protein Sci.
, vol.16
, pp. 2694-2702
-
-
Schweiker, K.L.1
Zarrine-Afsar, A.2
Davidson, A.R.3
Makhatadze, G.I.4
-
20
-
-
0036180211
-
EstB from Burkholderia gladioli: a novel esterase with a beta-lactamase fold reveals steric factors to discriminate between esterolytic and beta-lactam cleaving activity
-
Wagner U.G., Petersen E.I., Schwab H., and Kratky C. EstB from Burkholderia gladioli: a novel esterase with a beta-lactamase fold reveals steric factors to discriminate between esterolytic and beta-lactam cleaving activity. Protein Sci. 11 (2002) 467-478
-
(2002)
Protein Sci.
, vol.11
, pp. 467-478
-
-
Wagner, U.G.1
Petersen, E.I.2
Schwab, H.3
Kratky, C.4
-
21
-
-
34247474300
-
Efficient synthesis of simvastatin by use of whole-cell biocatalysis
-
Xie X., and Tang Y. Efficient synthesis of simvastatin by use of whole-cell biocatalysis. Appl. Environ. Microbiol. 73 (2007) 2054-2060
-
(2007)
Appl. Environ. Microbiol.
, vol.73
, pp. 2054-2060
-
-
Xie, X.1
Tang, Y.2
-
22
-
-
33751092257
-
Biosynthesis of lovastatin analogs with a broadly specific acyltransferase
-
Xie X., Watanabe K., Wojcicki W.A., Wang C.C., and Tang Y. Biosynthesis of lovastatin analogs with a broadly specific acyltransferase. Chem. Biol. 13 (2006) 1161-1169
-
(2006)
Chem. Biol.
, vol.13
, pp. 1161-1169
-
-
Xie, X.1
Watanabe, K.2
Wojcicki, W.A.3
Wang, C.C.4
Tang, Y.5
-
23
-
-
34547129077
-
Improving simvastatin bioconversion in Escherichia coli by deletion of bioH
-
Xie X., Wong W.W., and Tang Y. Improving simvastatin bioconversion in Escherichia coli by deletion of bioH. Metab. Eng. 9 (2007) 379-386
-
(2007)
Metab. Eng.
, vol.9
, pp. 379-386
-
-
Xie, X.1
Wong, W.W.2
Tang, Y.3
-
24
-
-
67650537065
-
acyltransferase mediated polyketide release from a fungal megasynthase
-
Xie X., Meehan M.J., Xu W., Dorrecstein P.C., and Tang Y. acyltransferase mediated polyketide release from a fungal megasynthase. J. Am. Chem. Soc. 131 (2009) 8388-8389
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 8388-8389
-
-
Xie, X.1
Meehan, M.J.2
Xu, W.3
Dorrecstein, P.C.4
Tang, Y.5
-
25
-
-
58149260829
-
Rational improvement of simvastatin synthase solubility in Escherichia coli leads to higher whole-cell biocatalytic activity
-
Xie X., Pashkov I., Gao X., Guerrero J.L., Yeates T.O., and Tang Y. Rational improvement of simvastatin synthase solubility in Escherichia coli leads to higher whole-cell biocatalytic activity. Biotechnol. Bioeng. 102 (2009) 20-28
-
(2009)
Biotechnol. Bioeng.
, vol.102
, pp. 20-28
-
-
Xie, X.1
Pashkov, I.2
Gao, X.3
Guerrero, J.L.4
Yeates, T.O.5
Tang, Y.6
-
26
-
-
33748302743
-
Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions
-
Zhang C., Griffith B.R., Fu Q., Albermann C., Fu X., Lee I.K., Li L.J., and Thorson J.S. Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions. Science 313 (2006) 1291-1294
-
(2006)
Science
, vol.313
, pp. 1291-1294
-
-
Zhang, C.1
Griffith, B.R.2
Fu, Q.3
Albermann, C.4
Fu, X.5
Lee, I.K.6
Li, L.J.7
Thorson, J.S.8
-
27
-
-
0032973026
-
Directed evolution converts subtilisin E into a functional equivalent of thermitase
-
Zhao H., and Arnold F.H. Directed evolution converts subtilisin E into a functional equivalent of thermitase. Protein Eng. 12 (1999) 47-53
-
(1999)
Protein Eng.
, vol.12
, pp. 47-53
-
-
Zhao, H.1
Arnold, F.H.2
-
28
-
-
57049185719
-
Engineering natural products using combinatorial biosynthesis and biocatalysis
-
Zhou H., Xie X., and Tang Y. Engineering natural products using combinatorial biosynthesis and biocatalysis. Curr. Opin. Biotechnol. 19 (2008) 590-596
-
(2008)
Curr. Opin. Biotechnol.
, vol.19
, pp. 590-596
-
-
Zhou, H.1
Xie, X.2
Tang, Y.3
|