T is not a problem. Current efforts to develop biosynthesis in

T is not a problem. Current efforts to develop biosynthesis in cell-free extracts [46] could allow for relatively straightforward integration of non-natural prosthetic groups and reagents in biosynthetic pathways. Thus working within the constraints of biology may ultimately prove unnecessary –even for enzyme engineers.Curr Opin Chem Biol. Author manuscript; available in PMC 2015 April 01.McIntosh et al.PageAcknowledgmentsThe authors acknowledge the support of the Jacobs Institute of Molecular Medicine at Caltech and the Office of Naval Research (grant N00014-11-1-0205). JAM is supported by an NIH Ruth L. Kirschstein National Research Service Award (F32GM101792) and CCF is supported by an NSF Graduate Research Fellowship. The content is solely the responsibility of the authors and does not represent the official views of any of the funding agencies. We thank Devin Trudeau, Jackson Cahn, Jane Wang, Ryan Lauchli, Sabine Brinkmann-Chen, Sheel Dodani, Tillman Heinisch, Todd Hyster, and Martin Enqvist for helpful comments on several versions of this review.NIH-PA Author Manuscript NIH-PA Author Manuscript NIH-PA Author ManuscriptReferences and recommended readingPapers of particular interest, published within the annual period of the review, have been highlighted as: ?Of special interest Of outstanding interest1. Keasling JD, Mendoza A, Baran PS. Synthesis: A constructive debate. Nature. 2012; 492(7428): 188?89. [PubMed: 23235869] 2. Blomberg R, Kries H, Pinkas DM, Mittl PR, Gr ter MG, Privett HK, Mayo SL, Hilvert D. Precision is essential for efficient catalysis in an evolved Kemp eliminase. Nature. 2013; 503(7476): 418?21. [PubMed: N-hexanoic-Try-Ile-(6)-amino hexanoic amide web 24132235] 3. Siegel JB, Zanghellini A, Lovick HM, Kiss G, Lambert AR, St Clair JL, Gallaher JL, Hilvert D, Gelb MH, Stoddard BL, Houk KN, et al. Computational design of an enzyme catalyst for a stereoselective bimolecular Diels-Alder reaction. Science. 2010; 329(5989):309?13. [PubMed: 20647463] 4. Gerlt JA, Babbitt PC. Enzyme (re)design: Lessons from natural evolution and computation. Curr Opin Chem Biol. 2009; 13(1):10?8. [PubMed: 19237310] 5. Glasner ME, Gerlt JA, Babbitt PC. Evolution of enzyme superfamilies. Curr Opin Chem Biol. 2006; 10(5):492?97. [PubMed: 16935022] 6. Dellus-Gur E, Toth-Petroczy A, Elias M, Tawfik DS. What makes a protein fold amenable to functional innovation? Fold polarity and stability tradeoffs. J Mol Biol. 2013; 425(14):2609?621. [PubMed: 23542341] 7. Guengerich FP, Munro AW. Unusual cytochrome P450 enzymes and reactions. J Biol Chem. 2013; 288(24):17065?7073. [PubMed: 23632016] 8. Guengerich FP. Common and uncommon cytochrome P450 reactions related to metabolism and chemical toxicity. Chem Res Toxicol. 2001; 14(6):611?50. [PubMed: 11409933] 9? Podust LM, Sherman DH. Diversity of P450 enzymes in the biosynthesis of natural products. Nat Prod Rep. 2012; 29(10):1251?266. This review discusses several interesting P450-catalyzed transformations that contribute to the biosynthesis of natural products. Several of the important mechanistic features of P450 catalysts including the role of the active-site threonine are explained. [PubMed: 22820933] 10? 1-Deoxynojirimycin web Whitehouse CJ, Bell SG, Wong LL. P450BM3 (CYP102A1). Connecting the dots. Chem Soc Rev. 2012; 41(3):1218?260. An excellent comprehensive look at the enzymology and applications of the well-studied P450BM3. [PubMed: 22008827] 11. Krest CM, Onderko EL, Yosca TH, Calixto JC, Karp RF, Livada J, Rittle J, Green MT. Reactive intermediates in cytoch.T is not a problem. Current efforts to develop biosynthesis in cell-free extracts [46] could allow for relatively straightforward integration of non-natural prosthetic groups and reagents in biosynthetic pathways. Thus working within the constraints of biology may ultimately prove unnecessary –even for enzyme engineers.Curr Opin Chem Biol. Author manuscript; available in PMC 2015 April 01.McIntosh et al.PageAcknowledgmentsThe authors acknowledge the support of the Jacobs Institute of Molecular Medicine at Caltech and the Office of Naval Research (grant N00014-11-1-0205). JAM is supported by an NIH Ruth L. Kirschstein National Research Service Award (F32GM101792) and CCF is supported by an NSF Graduate Research Fellowship. The content is solely the responsibility of the authors and does not represent the official views of any of the funding agencies. We thank Devin Trudeau, Jackson Cahn, Jane Wang, Ryan Lauchli, Sabine Brinkmann-Chen, Sheel Dodani, Tillman Heinisch, Todd Hyster, and Martin Enqvist for helpful comments on several versions of this review.NIH-PA Author Manuscript NIH-PA Author Manuscript NIH-PA Author ManuscriptReferences and recommended readingPapers of particular interest, published within the annual period of the review, have been highlighted as: ?Of special interest Of outstanding interest1. Keasling JD, Mendoza A, Baran PS. Synthesis: A constructive debate. Nature. 2012; 492(7428): 188?89. [PubMed: 23235869] 2. Blomberg R, Kries H, Pinkas DM, Mittl PR, Gr ter MG, Privett HK, Mayo SL, Hilvert D. Precision is essential for efficient catalysis in an evolved Kemp eliminase. Nature. 2013; 503(7476): 418?21. [PubMed: 24132235] 3. Siegel JB, Zanghellini A, Lovick HM, Kiss G, Lambert AR, St Clair JL, Gallaher JL, Hilvert D, Gelb MH, Stoddard BL, Houk KN, et al. Computational design of an enzyme catalyst for a stereoselective bimolecular Diels-Alder reaction. Science. 2010; 329(5989):309?13. [PubMed: 20647463] 4. Gerlt JA, Babbitt PC. Enzyme (re)design: Lessons from natural evolution and computation. Curr Opin Chem Biol. 2009; 13(1):10?8. [PubMed: 19237310] 5. Glasner ME, Gerlt JA, Babbitt PC. Evolution of enzyme superfamilies. Curr Opin Chem Biol. 2006; 10(5):492?97. [PubMed: 16935022] 6. Dellus-Gur E, Toth-Petroczy A, Elias M, Tawfik DS. What makes a protein fold amenable to functional innovation? Fold polarity and stability tradeoffs. J Mol Biol. 2013; 425(14):2609?621. [PubMed: 23542341] 7. Guengerich FP, Munro AW. Unusual cytochrome P450 enzymes and reactions. J Biol Chem. 2013; 288(24):17065?7073. [PubMed: 23632016] 8. Guengerich FP. Common and uncommon cytochrome P450 reactions related to metabolism and chemical toxicity. Chem Res Toxicol. 2001; 14(6):611?50. [PubMed: 11409933] 9? Podust LM, Sherman DH. Diversity of P450 enzymes in the biosynthesis of natural products. Nat Prod Rep. 2012; 29(10):1251?266. This review discusses several interesting P450-catalyzed transformations that contribute to the biosynthesis of natural products. Several of the important mechanistic features of P450 catalysts including the role of the active-site threonine are explained. [PubMed: 22820933] 10? Whitehouse CJ, Bell SG, Wong LL. P450BM3 (CYP102A1). Connecting the dots. Chem Soc Rev. 2012; 41(3):1218?260. An excellent comprehensive look at the enzymology and applications of the well-studied P450BM3. [PubMed: 22008827] 11. Krest CM, Onderko EL, Yosca TH, Calixto JC, Karp RF, Livada J, Rittle J, Green MT. Reactive intermediates in cytoch.