Matthew Hillwig

 MatthewL. Hillwig

Matthew L. Hillwig

  • Courses3
  • Reviews7

Biography

Robert Morris University - Chemistry & Biochemistry

Assistant Professor at Saint Vincent College
Higher Education
Matt
Hillwig
Pittsburgh, Pennsylvania
My research involves protein characterization and organic structure determination of terpenoids to elucidate gene function, using analytical tools, bioinformatics, protein biochemistry, and bacterial metabolic engineering.

Specialties: My specialty in part is biomarker identification using analytical tools including: stable isotope labeling, high-performance liquid chromatography (HPLC)-UV/Vis-ELSD, LC-mass spectrometry (LC-MS), gas-chromatography-MS (GC-MS), FT-IR, and multi-dimensional nuclear magnetic resonance (NMR) data analysis. Furthermore, I have experience in molecular biology, protein biochemistry, and enzymology.

For the earlier doctoral work I was awarded a competitive National Institutes of Health (NIH) Ruth L. Kirschstein National Research Service Award (NRSA) Individual Trainee Fellowship from 2004 to 2008. My research focused on metabolomics and biomarker identification.


Experience

  • Iowa State University

    Postdoctoral Research Associate

    Matthew worked at Iowa State University as a Postdoctoral Research Associate

  • Iowa State University

    Graduate Research Associate

    Matthew worked at Iowa State University as a Graduate Research Associate

  • Saint Vincent College

    Assistant Professor

    Matthew worked at Saint Vincent College as a Assistant Professor

  • Robert Morris University

    Part-time Faculty

    Lecturer in chemistry and Senior-level biology courses.

  • University of Pittsburgh

    Postdoctoral Associate

    Genome sequencing/mining and biochemical characterization of gene(s) suspected to be involved in the biosynthesis of anti-microbial natural products.

Education

  • Iowa State University

    Ph.D.

    Plant Biology

  • Iowa State University

    Postdoctoral Research Associate



  • Iowa State University

    Graduate Research Associate



  • The Pennsylvania State University

    B.S.

    Biology

Publications

  • Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1

    Angewandte Chemie International Edition

    Awakawa, T.; Mori, T.; Nakashima, Y.; Zhai, R.; Wong, C.P.; Hillwig, M.L.; Liu, X.; Abe, I. “Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1.” Angewandte Chemie International Edition 2018, 57 (23), 6810-6813.

  • Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1

    Angewandte Chemie International Edition

    Awakawa, T.; Mori, T.; Nakashima, Y.; Zhai, R.; Wong, C.P.; Hillwig, M.L.; Liu, X.; Abe, I. “Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1.” Angewandte Chemie International Edition 2018, 57 (23), 6810-6813.

  • Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity

    Chembiochem

    Zhu, Q.; Hillwig, M. L.; Doi, Y.; Liu, X., Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity. Chembiochem 2016, 17 (6), 466-70.

  • Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1

    Angewandte Chemie International Edition

    Awakawa, T.; Mori, T.; Nakashima, Y.; Zhai, R.; Wong, C.P.; Hillwig, M.L.; Liu, X.; Abe, I. “Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1.” Angewandte Chemie International Edition 2018, 57 (23), 6810-6813.

  • Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity

    Chembiochem

    Zhu, Q.; Hillwig, M. L.; Doi, Y.; Liu, X., Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity. Chembiochem 2016, 17 (6), 466-70.

  • A new family of iron-dependent halogenases acts on freestanding substrates.

    Nature Chemical Biology

    Hillwig ML, Liu X. A new family of iron-dependent halogenases acts on freestanding substrates. Nat Chem Biol. 2014 Sep 14. doi: 10.1038/nchembio.1625. [Epub ahead of print]

  • Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1

    Angewandte Chemie International Edition

    Awakawa, T.; Mori, T.; Nakashima, Y.; Zhai, R.; Wong, C.P.; Hillwig, M.L.; Liu, X.; Abe, I. “Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1.” Angewandte Chemie International Edition 2018, 57 (23), 6810-6813.

  • Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity

    Chembiochem

    Zhu, Q.; Hillwig, M. L.; Doi, Y.; Liu, X., Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity. Chembiochem 2016, 17 (6), 466-70.

  • A new family of iron-dependent halogenases acts on freestanding substrates.

    Nature Chemical Biology

    Hillwig ML, Liu X. A new family of iron-dependent halogenases acts on freestanding substrates. Nat Chem Biol. 2014 Sep 14. doi: 10.1038/nchembio.1625. [Epub ahead of print]

  • Unified biogenesis of ambiguine, fischerindole, hapalindole and welwitindolinone: identification of a monogeranylated indolenine as a cryptic common biosynthetic intermediate by an unusual magnesium-dependent aromatic prenyltransferase

    Chemical Communications

    Liu, X.; Hillwig, M. L.; Koharudin, L. M. I.; Gronenborn, A. M., Unified biogenesis of ambiguine, fischerindole, hapalindole and welwitindolinone: identification of a monogeranylated indolenine as a cryptic common biosynthetic intermediate by an unusual magnesium-dependent aromatic prenyltransferase. Chemical Communications 2016, 52 (8), 1737-1740.

  • Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1

    Angewandte Chemie International Edition

    Awakawa, T.; Mori, T.; Nakashima, Y.; Zhai, R.; Wong, C.P.; Hillwig, M.L.; Liu, X.; Abe, I. “Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1.” Angewandte Chemie International Edition 2018, 57 (23), 6810-6813.

  • Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity

    Chembiochem

    Zhu, Q.; Hillwig, M. L.; Doi, Y.; Liu, X., Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity. Chembiochem 2016, 17 (6), 466-70.

  • A new family of iron-dependent halogenases acts on freestanding substrates.

    Nature Chemical Biology

    Hillwig ML, Liu X. A new family of iron-dependent halogenases acts on freestanding substrates. Nat Chem Biol. 2014 Sep 14. doi: 10.1038/nchembio.1625. [Epub ahead of print]

  • Unified biogenesis of ambiguine, fischerindole, hapalindole and welwitindolinone: identification of a monogeranylated indolenine as a cryptic common biosynthetic intermediate by an unusual magnesium-dependent aromatic prenyltransferase

    Chemical Communications

    Liu, X.; Hillwig, M. L.; Koharudin, L. M. I.; Gronenborn, A. M., Unified biogenesis of ambiguine, fischerindole, hapalindole and welwitindolinone: identification of a monogeranylated indolenine as a cryptic common biosynthetic intermediate by an unusual magnesium-dependent aromatic prenyltransferase. Chemical Communications 2016, 52 (8), 1737-1740.

  • Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis

    Proceedings of the National Academy of Sciences

    Mafu, S.; Jia, M.; Zi, J.; Morrone, D.; Wu, Y.; Xu, M.; Hillwig, M. L.; Peters, R. J. “Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis.” Proceedings of the National Academy of Sciences of the U.S.A. 2016, 113 (9), 2526-2531.

  • Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis

    Proceedings of the National Academy of Sciences

    Mafu, S.; Jia, M.; Zi, J.; Morrone, D.; Wu, Y.; Xu, M.; Hillwig, M. L.; Peters, R. J., Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis. Proceedings of the National Academy of Sciences 2016, 113 (9), 2526-2531.

  • Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1

    Angewandte Chemie International Edition

    Awakawa, T.; Mori, T.; Nakashima, Y.; Zhai, R.; Wong, C.P.; Hillwig, M.L.; Liu, X.; Abe, I. “Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1.” Angewandte Chemie International Edition 2018, 57 (23), 6810-6813.

  • Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity

    Chembiochem

    Zhu, Q.; Hillwig, M. L.; Doi, Y.; Liu, X., Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity. Chembiochem 2016, 17 (6), 466-70.

  • A new family of iron-dependent halogenases acts on freestanding substrates.

    Nature Chemical Biology

    Hillwig ML, Liu X. A new family of iron-dependent halogenases acts on freestanding substrates. Nat Chem Biol. 2014 Sep 14. doi: 10.1038/nchembio.1625. [Epub ahead of print]

  • Unified biogenesis of ambiguine, fischerindole, hapalindole and welwitindolinone: identification of a monogeranylated indolenine as a cryptic common biosynthetic intermediate by an unusual magnesium-dependent aromatic prenyltransferase

    Chemical Communications

    Liu, X.; Hillwig, M. L.; Koharudin, L. M. I.; Gronenborn, A. M., Unified biogenesis of ambiguine, fischerindole, hapalindole and welwitindolinone: identification of a monogeranylated indolenine as a cryptic common biosynthetic intermediate by an unusual magnesium-dependent aromatic prenyltransferase. Chemical Communications 2016, 52 (8), 1737-1740.

  • Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis

    Proceedings of the National Academy of Sciences

    Mafu, S.; Jia, M.; Zi, J.; Morrone, D.; Wu, Y.; Xu, M.; Hillwig, M. L.; Peters, R. J. “Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis.” Proceedings of the National Academy of Sciences of the U.S.A. 2016, 113 (9), 2526-2531.

  • Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis

    Proceedings of the National Academy of Sciences

    Mafu, S.; Jia, M.; Zi, J.; Morrone, D.; Wu, Y.; Xu, M.; Hillwig, M. L.; Peters, R. J., Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis. Proceedings of the National Academy of Sciences 2016, 113 (9), 2526-2531.

  • Probing labdane-related diterpenoid biosynthesis in the fungal genus Aspergillus

    Journal of Natural Products

    Xu M, Hillwig ML, Tiernan MS, Peters RJ. “Probing labdane-related diterpenoid biosynthesis in the fungal genus Aspergillus.” Journal of Natural Products 2017, 80 (2), 328-33.

  • Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1

    Angewandte Chemie International Edition

    Awakawa, T.; Mori, T.; Nakashima, Y.; Zhai, R.; Wong, C.P.; Hillwig, M.L.; Liu, X.; Abe, I. “Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1.” Angewandte Chemie International Edition 2018, 57 (23), 6810-6813.

  • Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity

    Chembiochem

    Zhu, Q.; Hillwig, M. L.; Doi, Y.; Liu, X., Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity. Chembiochem 2016, 17 (6), 466-70.

  • A new family of iron-dependent halogenases acts on freestanding substrates.

    Nature Chemical Biology

    Hillwig ML, Liu X. A new family of iron-dependent halogenases acts on freestanding substrates. Nat Chem Biol. 2014 Sep 14. doi: 10.1038/nchembio.1625. [Epub ahead of print]

  • Unified biogenesis of ambiguine, fischerindole, hapalindole and welwitindolinone: identification of a monogeranylated indolenine as a cryptic common biosynthetic intermediate by an unusual magnesium-dependent aromatic prenyltransferase

    Chemical Communications

    Liu, X.; Hillwig, M. L.; Koharudin, L. M. I.; Gronenborn, A. M., Unified biogenesis of ambiguine, fischerindole, hapalindole and welwitindolinone: identification of a monogeranylated indolenine as a cryptic common biosynthetic intermediate by an unusual magnesium-dependent aromatic prenyltransferase. Chemical Communications 2016, 52 (8), 1737-1740.

  • Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis

    Proceedings of the National Academy of Sciences

    Mafu, S.; Jia, M.; Zi, J.; Morrone, D.; Wu, Y.; Xu, M.; Hillwig, M. L.; Peters, R. J. “Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis.” Proceedings of the National Academy of Sciences of the U.S.A. 2016, 113 (9), 2526-2531.

  • Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis

    Proceedings of the National Academy of Sciences

    Mafu, S.; Jia, M.; Zi, J.; Morrone, D.; Wu, Y.; Xu, M.; Hillwig, M. L.; Peters, R. J., Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis. Proceedings of the National Academy of Sciences 2016, 113 (9), 2526-2531.

  • Probing labdane-related diterpenoid biosynthesis in the fungal genus Aspergillus

    Journal of Natural Products

    Xu M, Hillwig ML, Tiernan MS, Peters RJ. “Probing labdane-related diterpenoid biosynthesis in the fungal genus Aspergillus.” Journal of Natural Products 2017, 80 (2), 328-33.

  • Efficient heterocyclisation by (di)terpene synthases

    Chemical Communications

    Mafu S, Potter KC, Hillwig ML, Schulte S, Criswell J, Peters RJ. “Efficient heterocyclisation by (di)terpene synthases.” Chemical Communications 2015 18;51(70):13485-7.

  • Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1

    Angewandte Chemie International Edition

    Awakawa, T.; Mori, T.; Nakashima, Y.; Zhai, R.; Wong, C.P.; Hillwig, M.L.; Liu, X.; Abe, I. “Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1.” Angewandte Chemie International Edition 2018, 57 (23), 6810-6813.

  • Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity

    Chembiochem

    Zhu, Q.; Hillwig, M. L.; Doi, Y.; Liu, X., Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity. Chembiochem 2016, 17 (6), 466-70.

  • A new family of iron-dependent halogenases acts on freestanding substrates.

    Nature Chemical Biology

    Hillwig ML, Liu X. A new family of iron-dependent halogenases acts on freestanding substrates. Nat Chem Biol. 2014 Sep 14. doi: 10.1038/nchembio.1625. [Epub ahead of print]

  • Unified biogenesis of ambiguine, fischerindole, hapalindole and welwitindolinone: identification of a monogeranylated indolenine as a cryptic common biosynthetic intermediate by an unusual magnesium-dependent aromatic prenyltransferase

    Chemical Communications

    Liu, X.; Hillwig, M. L.; Koharudin, L. M. I.; Gronenborn, A. M., Unified biogenesis of ambiguine, fischerindole, hapalindole and welwitindolinone: identification of a monogeranylated indolenine as a cryptic common biosynthetic intermediate by an unusual magnesium-dependent aromatic prenyltransferase. Chemical Communications 2016, 52 (8), 1737-1740.

  • Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis

    Proceedings of the National Academy of Sciences

    Mafu, S.; Jia, M.; Zi, J.; Morrone, D.; Wu, Y.; Xu, M.; Hillwig, M. L.; Peters, R. J. “Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis.” Proceedings of the National Academy of Sciences of the U.S.A. 2016, 113 (9), 2526-2531.

  • Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis

    Proceedings of the National Academy of Sciences

    Mafu, S.; Jia, M.; Zi, J.; Morrone, D.; Wu, Y.; Xu, M.; Hillwig, M. L.; Peters, R. J., Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis. Proceedings of the National Academy of Sciences 2016, 113 (9), 2526-2531.

  • Probing labdane-related diterpenoid biosynthesis in the fungal genus Aspergillus

    Journal of Natural Products

    Xu M, Hillwig ML, Tiernan MS, Peters RJ. “Probing labdane-related diterpenoid biosynthesis in the fungal genus Aspergillus.” Journal of Natural Products 2017, 80 (2), 328-33.

  • Efficient heterocyclisation by (di)terpene synthases

    Chemical Communications

    Mafu S, Potter KC, Hillwig ML, Schulte S, Criswell J, Peters RJ. “Efficient heterocyclisation by (di)terpene synthases.” Chemical Communications 2015 18;51(70):13485-7.

  • Structural basis for halogenation by iron- and 2-oxo-glutarate-dependent enzyme WelO5

    Nature Chemical Biology

    Mitchell, A. J.; Zhu, Q.; Maggiolo, A. O.; Ananth, N. R.; Hillwig, M. L.; Liu, X.; Boal, A. K., Structural basis for halogenation by iron- and 2-oxo-glutarate-dependent enzyme WelO5. Nature Chemical Biology 2016, 12 (8), 636-40.

  • Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1

    Angewandte Chemie International Edition

    Awakawa, T.; Mori, T.; Nakashima, Y.; Zhai, R.; Wong, C.P.; Hillwig, M.L.; Liu, X.; Abe, I. “Molecular Insight into the Mg2+‐Dependent Allosteric Control of Indole Prenylation by Aromatic Prenyltransferase AmbP1.” Angewandte Chemie International Edition 2018, 57 (23), 6810-6813.

  • Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity

    Chembiochem

    Zhu, Q.; Hillwig, M. L.; Doi, Y.; Liu, X., Aliphatic Halogenase Enables Late-Stage C−H Functionalization: Selective Synthesis of a Brominated Fischerindole Alkaloid with Enhanced Antibacterial Activity. Chembiochem 2016, 17 (6), 466-70.

  • A new family of iron-dependent halogenases acts on freestanding substrates.

    Nature Chemical Biology

    Hillwig ML, Liu X. A new family of iron-dependent halogenases acts on freestanding substrates. Nat Chem Biol. 2014 Sep 14. doi: 10.1038/nchembio.1625. [Epub ahead of print]

  • Unified biogenesis of ambiguine, fischerindole, hapalindole and welwitindolinone: identification of a monogeranylated indolenine as a cryptic common biosynthetic intermediate by an unusual magnesium-dependent aromatic prenyltransferase

    Chemical Communications

    Liu, X.; Hillwig, M. L.; Koharudin, L. M. I.; Gronenborn, A. M., Unified biogenesis of ambiguine, fischerindole, hapalindole and welwitindolinone: identification of a monogeranylated indolenine as a cryptic common biosynthetic intermediate by an unusual magnesium-dependent aromatic prenyltransferase. Chemical Communications 2016, 52 (8), 1737-1740.

  • Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis

    Proceedings of the National Academy of Sciences

    Mafu, S.; Jia, M.; Zi, J.; Morrone, D.; Wu, Y.; Xu, M.; Hillwig, M. L.; Peters, R. J. “Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis.” Proceedings of the National Academy of Sciences of the U.S.A. 2016, 113 (9), 2526-2531.

  • Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis

    Proceedings of the National Academy of Sciences

    Mafu, S.; Jia, M.; Zi, J.; Morrone, D.; Wu, Y.; Xu, M.; Hillwig, M. L.; Peters, R. J., Probing the promiscuity of ent-kaurene oxidases via combinatorial biosynthesis. Proceedings of the National Academy of Sciences 2016, 113 (9), 2526-2531.

  • Probing labdane-related diterpenoid biosynthesis in the fungal genus Aspergillus

    Journal of Natural Products

    Xu M, Hillwig ML, Tiernan MS, Peters RJ. “Probing labdane-related diterpenoid biosynthesis in the fungal genus Aspergillus.” Journal of Natural Products 2017, 80 (2), 328-33.

  • Efficient heterocyclisation by (di)terpene synthases

    Chemical Communications

    Mafu S, Potter KC, Hillwig ML, Schulte S, Criswell J, Peters RJ. “Efficient heterocyclisation by (di)terpene synthases.” Chemical Communications 2015 18;51(70):13485-7.

  • Structural basis for halogenation by iron- and 2-oxo-glutarate-dependent enzyme WelO5

    Nature Chemical Biology

    Mitchell, A. J.; Zhu, Q.; Maggiolo, A. O.; Ananth, N. R.; Hillwig, M. L.; Liu, X.; Boal, A. K., Structural basis for halogenation by iron- and 2-oxo-glutarate-dependent enzyme WelO5. Nature Chemical Biology 2016, 12 (8), 636-40.

  • Discovery of a Promiscuous Non-Heme Iron Halogenase in Ambiguine Alkaloid Biogenesis: Implication for an Evolvable Enzyme Family for Late-Stage Halogenation of Aliphatic Carbons in Small Molecules

    Angewandte Chemie International Edition

    Hillwig, M. L.; Zhu, Q.; Ittiamornkul, K.; Liu, X., Discovery of a Promiscuous Non-Heme Iron Halogenase in Ambiguine Alkaloid Biogenesis: Implication for an Evolvable Enzyme Family for Late-Stage Halogenation of Aliphatic Carbons in Small Molecules. Angewandte Chemie International Edition 2016, 55 (19), 5780-4.

BIOL 4000

2.5(1)

CHEM 1210

1.8(5)

CHEMG 1210

1(1)