Literature DB >> 30770407

Structure-Function Analysis Indicates that an Active-Site Water Molecule Participates in Dimethylsulfoniopropionate Cleavage by DddK.

Ming Peng1, Xiu-Lan Chen1,2, Dian Zhang1, Xiu-Juan Wang1, Ning Wang1, Peng Wang1, Jonathan D Todd3, Yu-Zhong Zhang1,4,2, Chun-Yang Li5,4,6.   

Abstract

The osmolyte dimethylsulfoniopropionate (DMSP) is produced in petagram quantities in marine environments and has important roles in global sulfur and carbon cycling. Many marine microorganisms catabolize DMSP via DMSP lyases, generating the climate-active gas dimethyl sulfide (DMS). DMS oxidation products participate in forming cloud condensation nuclei and, thus, may influence weather and climate. SAR11 bacteria are the most abundant marine heterotrophic bacteria; many of them contain the DMSP lyase DddK, and their dddK transcripts are relatively abundant in seawater. In a recently described catalytic mechanism for DddK, Tyr64 is predicted to act as the catalytic base initiating the β-elimination reaction of DMSP. Tyr64 was proposed to be deprotonated by coordination to the metal cofactor or its neighboring His96. To further probe this mechanism, we purified and characterized the DddK protein from Pelagibacter ubique strain HTCC1062 and determined the crystal structures of wild-type DddK and its Y64A and Y122A mutants (bearing a change of Y to A at position 64 or 122, respectively), where the Y122A mutant is complexed with DMSP. The structural and mutational analyses largely support the catalytic role of Tyr64, but not the method of its deprotonation. Our data indicate that an active water molecule in the active site of DddK plays an important role in the deprotonation of Tyr64 and that this is far more likely than coordination to the metal or His96. Sequence alignment and phylogenetic analysis suggest that the proposed catalytic mechanism of DddK has universal significance. Our results provide new mechanistic insights into DddK and enrich our understanding of DMS generation by SAR11 bacteria.IMPORTANCE The climate-active gas dimethyl sulfide (DMS) plays an important role in global sulfur cycling and atmospheric chemistry. DMS is mainly produced through the bacterial cleavage of marine dimethylsulfoniopropionate (DMSP). When released into the atmosphere from the oceans, DMS can be photochemically oxidized into DMSO or sulfate aerosols, which form cloud condensation nuclei that influence the reflectivity of clouds and, thereby, global temperature. SAR11 bacteria are the most abundant marine heterotrophic bacteria, and many of them contain DMSP lyase DddK to cleave DMSP, generating DMS. In this study, based on structural analyses and mutational assays, we revealed the catalytic mechanism of DddK, which has universal significance in SAR11 bacteria. This study provides new insights into the catalytic mechanism of DddK, leading to a better understanding of how SAR11 bacteria generate DMS.
Copyright © 2019 American Society for Microbiology.

Entities:  

Keywords:  DMS generation; DMSP; DMSP lyase DddK; SAR11; catalytic mechanism

Year:  2019        PMID: 30770407      PMCID: PMC6450030          DOI: 10.1128/AEM.03127-18

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  32 in total

1.  Molecular insight into bacterial cleavage of oceanic dimethylsulfoniopropionate into dimethyl sulfide.

Authors:  Chun-Yang Li; Tian-Di Wei; Sheng-Hui Zhang; Xiu-Lan Chen; Xiang Gao; Peng Wang; Bin-Bin Xie; Hai-Nan Su; Qi-Long Qin; Xi-Ying Zhang; Juan Yu; Hong-Hai Zhang; Bai-Cheng Zhou; Gui-Peng Yang; Yu-Zhong Zhang
Journal:  Proc Natl Acad Sci U S A       Date:  2014-01-06       Impact factor: 11.205

2.  The Dimethylsulfoniopropionate (DMSP) Lyase and Lyase-Like Cupin Family Consists of Bona Fide DMSP lyases as Well as Other Enzymes with Unknown Function.

Authors:  Lei Lei; Kesava Phaneendra Cherukuri; Uria Alcolombri; Diana Meltzer; Dan S Tawfik
Journal:  Biochemistry       Date:  2018-04-03       Impact factor: 3.162

3.  Structural and Biochemical Insights into Dimethylsulfoniopropionate Cleavage by Cofactor-Bound DddK from the Prolific Marine Bacterium Pelagibacter.

Authors:  Nicholas J Schnicker; Saumya M De Silva; Jonathan D Todd; Mishtu Dey
Journal:  Biochemistry       Date:  2017-05-30       Impact factor: 3.162

4.  The abundant marine bacterium Pelagibacter simultaneously catabolizes dimethylsulfoniopropionate to the gases dimethyl sulfide and methanethiol.

Authors:  Jing Sun; Jonathan D Todd; J Cameron Thrash; Yanping Qian; Michael C Qian; Ben Temperton; Jiazhen Guo; Emily K Fowler; Joshua T Aldrich; Carrie D Nicora; Mary S Lipton; Richard D Smith; Patrick De Leenheer; Samuel H Payne; Andrew W B Johnston; Cleo L Davie-Martin; Kimberly H Halsey; Stephen J Giovannoni
Journal:  Nat Microbiol       Date:  2016-05-16       Impact factor: 17.745

5.  PHENIX: a comprehensive Python-based system for macromolecular structure solution.

Authors:  Paul D Adams; Pavel V Afonine; Gábor Bunkóczi; Vincent B Chen; Ian W Davis; Nathaniel Echols; Jeffrey J Headd; Li-Wei Hung; Gary J Kapral; Ralf W Grosse-Kunstleve; Airlie J McCoy; Nigel W Moriarty; Robert Oeffner; Randy J Read; David C Richardson; Jane S Richardson; Thomas C Terwilliger; Peter H Zwart
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2010-01-22

6.  Dimethylsulfoniopropionate-dependent demethylase (DmdA) from Pelagibacter ubique and Silicibacter pomeroyi.

Authors:  Chris R Reisch; Mary Ann Moran; William B Whitman
Journal:  J Bacteriol       Date:  2008-10-10       Impact factor: 3.490

7.  DSYB catalyses the key step of dimethylsulfoniopropionate biosynthesis in many phytoplankton.

Authors:  Andrew R J Curson; Beth T Williams; Benjamin J Pinchbeck; Leanne P Sims; Ana Bermejo Martínez; Peter Paolo L Rivera; Deepak Kumaresan; Elena Mercadé; Lewis G Spurgin; Ornella Carrión; Simon Moxon; Rose Ann Cattolico; Unnikrishnan Kuzhiumparambil; Paul Guagliardo; Peta L Clode; Jean-Baptiste Raina; Jonathan D Todd
Journal:  Nat Microbiol       Date:  2018-02-26       Impact factor: 17.745

8.  Mechanistic Insights into Dimethylsulfoniopropionate Lyase DddY, a New Member of the Cupin Superfamily.

Authors:  Chun-Yang Li; Dian Zhang; Xiu-Lan Chen; Peng Wang; Wei-Ling Shi; Ping-Yi Li; Xi-Ying Zhang; Qi-Long Qin; Jonathan D Todd; Yu-Zhong Zhang
Journal:  J Mol Biol       Date:  2017-10-26       Impact factor: 5.469

9.  Structural and regulatory genes required to make the gas dimethyl sulfide in bacteria.

Authors:  Jonathan D Todd; Rachel Rogers; You Guo Li; Margaret Wexler; Philip L Bond; Lei Sun; Andrew R J Curson; Gill Malin; Michael Steinke; Andrew W B Johnston
Journal:  Science       Date:  2007-02-02       Impact factor: 47.728

10.  Biochemical, Kinetic, and Spectroscopic Characterization of Ruegeria pomeroyi DddW--A Mononuclear Iron-Dependent DMSP Lyase.

Authors:  Adam E Brummett; Nicholas J Schnicker; Alexander Crider; Jonathan D Todd; Mishtu Dey
Journal:  PLoS One       Date:  2015-05-19       Impact factor: 3.240

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