Organometallic Complex Formed by an Unconventional Radical S-Adenosylmethionine Enzyme

被引:17
|
作者
Dong, Min [1 ]
Horitani, Masaki [2 ]
Dzikovski, Boris [1 ]
Pandelia, Maria-Eirini [3 ]
Krebs, Carsten [4 ,5 ]
Freed, Jack H. [1 ]
Hoffman, Brian M. [2 ]
Lin, Hening [1 ,6 ]
机构
[1] Cornell Univ, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
[2] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[3] Brandeis Univ, Dept Biochem, Waltham, MA 02453 USA
[4] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[5] Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
[6] Cornell Univ, Howard Hughes Med Inst, Ithaca, NY 14853 USA
关键词
BIOSYNTHESIS; MECHANISM; INTERMEDIATE; INHIBITION; CATALYSIS;
D O I
10.1021/jacs.6b04155
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Pyrococcus horikoshii Dph2 (PhDph2) is an unusual radical S-adenosylmethionine (SAM) enzyme involved in the first step of diphthamide biosynthesis. It catalyzes the reaction by cleaving SAM to generate a 3-amino-3-carboxypropyl (ACP) radical. To probe the reaction mechanism, we synthesized a SAM analogue (SAMcA), in which the ACP group of SAM is replaced with a 3-carboxyally1 group. SAMcA. is cleaved by PhDph2, yielding a paramagnetic (S = 1/2) species, which is assigned to a complex formed between the reaction product, alpha-sulfinyl-3-butenoic acid, and the [4Fe-4S] cluster. Electron nuclear double resonance (ENDOR) measurements with C-13 and H-2 isotopically labeled SAM(CA) support a sr-complex between the C=C double bond of asulfinyl-3-butenoic acid and the unique iron of the [4Fe-4S] cluster. This is the first example of a radical SAM-related [4Fe-4S](+) cluster forming an organometallic complex with an alkene, shedding additional light on the mechanism of PhDph2 and expanding our current notions for the reactivity of [4Fe-4S] clusters in radical SAM enzymes.
引用
收藏
页码:9755 / 9758
页数:4
相关论文
共 50 条
  • [21] S-Adenosylmethionine
    Lu, SC
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2000, 32 (04): : 391 - 395
  • [22] Radical S-Adenosylmethionine Enzymes in Human Health and Disease
    Landgraf, Bradley J.
    McCarthy, Erin L.
    Booker, Squire J.
    ANNUAL REVIEW OF BIOCHEMISTRY, VOL 85, 2016, 85 : 485 - 514
  • [23] S-adenosylmethionine
    Florsheim, Amanda
    Dramard, Valerie
    Bottiglieri, Teodoro
    Mischoulon, David
    VETERINARY MEDICINE, 2008, 103 (07) : A1 - A8
  • [24] S-adenosylmethionine
    Davidson, G
    COMPENDIUM ON CONTINUING EDUCATION FOR THE PRACTICING VETERINARIAN, 2002, 24 (08): : 600 - +
  • [25] Radical S-adenosylmethionine enzymes: Mechanism, control and function
    Challand, Martin R.
    Driesener, Rebecca C.
    Roach, Peter L.
    NATURAL PRODUCT REPORTS, 2011, 28 (10) : 1696 - 1721
  • [26] Radical S-Adenosylmethionine Enzymes Involved in RiPP Biosynthesis
    Mahanta, Nilkamal
    Hudson, Graham A.
    Mitchell, Douglas A.
    BIOCHEMISTRY, 2017, 56 (40) : 5229 - 5244
  • [27] METHIONINE ADENOSYLTRANSFERASE (S-ADENOSYLMETHIONINE SYNTHETASE) AND S-ADENOSYLMETHIONINE DECARBOXYLASE
    TABOR, CW
    TABOR, H
    ADVANCES IN ENZYMOLOGY AND RELATED AREAS OF MOLECULAR BIOLOGY, 1984, 56 : 251 - 282
  • [28] Self-sacrifice in radical S-adenosylmethionine proteins
    Booker, Squire J.
    Cicchillo, Robert M.
    Grove, Tyler L.
    CURRENT OPINION IN CHEMICAL BIOLOGY, 2007, 11 (05) : 543 - 552
  • [29] AFFINITY ADSORBENT FOR AN S-ADENOSYLMETHIONINE DEPENDENT METHYLTRANSFERASE ENZYME
    MACK, J
    SLAYTOR, M
    FEDERATION PROCEEDINGS, 1976, 35 (07) : 1752 - 1752
  • [30] Reconstitution and Substrate Specificity of the Thioether-Forming Radical S-Adenosylmethionine Enzyme in Freyrasin Biosynthesis
    Precord, Timothy W.
    Mahanta, Nilkamal
    Mitchell, Douglas A.
    ACS CHEMICAL BIOLOGY, 2019, 14 (09) : 1981 - 1989