Hybridization of Particulate Methane Monooxygenase by Methanobactin-Modified AuNPs

被引:0
|
作者
Xin, Jia-Ying [1 ,2 ]
Sun, Li-Rui [1 ]
Lin, Hui-Ying [1 ]
Zhang, Shuai [1 ]
Xia, Chun-Gu [2 ]
机构
[1] Harbin Univ Commerce, Key Lab Food Sci & Engn, Harbin 150076, Heilongjiang, Peoples R China
[2] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Gansu, Peoples R China
来源
MOLECULES | 2019年 / 24卷 / 22期
基金
中国国家自然科学基金;
关键词
AuNPs; nanobiohybrids; electron donor; hydroquinone; methanobactin; particulate methane monooxygenase; METHYLOCOCCUS-CAPSULATUS BATH; METHYLOSINUS-TRICHOSPORIUM; HYDROGEN-PEROXIDE; ACTIVE-SITE; COPPER; PURIFICATION; BINDING;
D O I
10.3390/molecules24224027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Particulate methane monooxygenase (pMMO) is a characteristic membrane-bound metalloenzyme of methane-oxidizing bacteria that can catalyze the bioconversion of methane to methanol. However, in order to achieve pMMO-based continuous methane-to-methanol bioconversion, the problems of reducing power in vitro regeneration and pMMO stability need to be overcome. Methanobactin (Mb) is a small copper-chelating molecule that functions not only as electron carrier for pMMO catalysis and pMMO protector against oxygen radicals, but also as an agent for copper acquisition and uptake. In order to improve the activity and stability of pMMO, methanobactin-Cu (Mb-Cu)-modified gold nanoparticle (AuNP)-pMMO nanobiohybrids were straightforwardly synthesized via in situ reduction of HAuCl4 to AuNPs in a membrane fraction before further association with Mb-Cu. Mb-Cu modification can greatly improve the activity and stability of pMMO in the AuNP-pMMO nanobiohybrids. It is shown that the Mb-Cu-modified AuNP-pMMO nanobiohybrids can persistently catalyze the conversion of methane to methanol with hydroquinone as electron donor. The artificial heterogeneous nanobiohybrids exhibited excellent reusability and reproducibility in three cycles of catalysis, and they provide a model for achieving hydroquinone-driven conversion of methane to methanol.
引用
收藏
页数:17
相关论文
共 50 条
  • [31] Quantum refinement of the crystal structure of particulate methane monooxygenase
    Cao, Lili
    Caldararu, Octav
    Ryde, Ulf
    JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY, 2017, 22 : S123 - S123
  • [32] Structure and activity of particulate methane monooxygenase arrays in methanotrophs
    Yanan Zhu
    Christopher W. Koo
    C. Keith Cassidy
    Matthew C. Spink
    Tao Ni
    Laura C. Zanetti-Domingues
    Benji Bateman
    Marisa L. Martin-Fernandez
    Juan Shen
    Yuewen Sheng
    Yun Song
    Zhengyi Yang
    Amy C. Rosenzweig
    Peijun Zhang
    Nature Communications, 13
  • [33] MmoD regulates soluble methane monooxygenase and methanobactin production in Methylosinus trichosporium OB3b
    Peng, Peng
    Yang, Junwon
    Dispirito, Alan A.
    Semrau, Jeremy D.
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2023, 89 (12)
  • [34] Methane activation by a single copper center in particulate methane monooxygenase: A computational study
    Morris, Robert H.
    INORGANICA CHIMICA ACTA, 2020, 503 (503)
  • [35] Evidence for Oxygen Binding at the Active Site of Particulate Methane Monooxygenase
    Culpepper, Megen A.
    Cutsail, George E., III
    Hoffman, Brian M.
    Rosenzweig, Amy C.
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (18) : 7640 - 7643
  • [36] Recovery of particulate methane monooxygenase structure and activity in a lipid bilayer
    Koo, Christopher W.
    Tucci, Frank J.
    He, Yuan
    Rosenzweig, Amy C.
    SCIENCE, 2022, 375 (6586) : 1287 - +
  • [37] Particulate methane monooxygenase contains only mononuclear copper centers
    Ross, Matthew O.
    MacMillan, Fraser
    Wang, Jingzhou
    Nisthal, Alex
    Lawton, Thomas J.
    Olafson, Barry D.
    Mayo, Stephen L.
    Rosenzweig, Amy C.
    Hoffman, Brian M.
    SCIENCE, 2019, 364 (6440) : 566 - +
  • [38] Methane oxidation by the copper methane monooxygenase: Before and after the cryogenic electron microscopy structure of particulate methane monooxygenase from Methylococcus capsulatus (Bath)
    Chan, Sunney, I
    Wang, Vincent C-C
    Chen, Peter P-Y
    Yu, Steve S-F
    JOURNAL OF THE CHINESE CHEMICAL SOCIETY, 2022, 69 (08) : 1147 - 1158
  • [39] Biological methane oxidation: Regulation, biochemistry, and active site structure of particulate methane monooxygenase
    Lieberman, RL
    Rosenzweig, AC
    CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2004, 39 (03) : 147 - 164
  • [40] In situ measurement of methane fluxes and analysis of transcribed particulate methane monooxygenase in desert soils
    Angel, Roey
    Conrad, Ralf
    ENVIRONMENTAL MICROBIOLOGY, 2009, 11 (10) : 2598 - 2610