TY - JOUR
T1 - Bacteria are important dimethylsulfoniopropionate producers in coastal sediments
AU - Williams, Beth T.
AU - Cowles, Kasha
AU - Bermejo Martínez, Ana
AU - Curson, Andrew R.J.
AU - Zheng, Yanfen
AU - Liu, Jingli
AU - Newton-Payne, Simone
AU - Hind, Andrew J.
AU - Li, Chun Yang
AU - Rivera, Peter Paolo L.
AU - Carrión, Ornella
AU - Liu, Ji
AU - Spurgin, Lewis G.
AU - Brearley, Charles A.
AU - Mackenzie, Brett Wagner
AU - Pinchbeck, Benjamin J.
AU - Peng, Ming
AU - Pratscher, Jennifer
AU - Zhang, Xiao Hua
AU - Zhang, Yu Zhong
AU - Murrell, J. Colin
AU - Todd, Jonathan D.
N1 - P Rivera was not affiliated to SAMS at the time of publication,
Funding Information:
Funding from the Natural Environmental Research Council (NE/N002385, NE/ P012671 and NE/S001352) supported work in J.D.T.’s laboratory. Funding from the National Natural Science Foundation of China (grant numbers 91751202 and 41730530) supported the research in X.-H.Z.’s laboratory. B.T.W. was supported by a NERC EnvEast grant (NE/L002582/1). A.B.M. and K.C. were supported by the BBSRC Norwich Research Park Biosciences Doctoral Training Partnership grant number BB/M011216/1. J.P. was supported by a NERC Independent Research Fellowship (NE/L010771/2). We thank P. Wells for general technical support, and P. Nelson and R. Whiting at the CEFAS, Lowestoft for sediment nutrient analysis. We acknowledge the Tara Oceans Consortium for providing metagenomic sequence data. We also thank the late R. Kiene, whose work on DMSP was an inspiration for this study.
Publisher Copyright:
© 2019, The Author(s), under exclusive licence to Springer Nature Limited.
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2019/11/1
Y1 - 2019/11/1
N2 - Dimethylsulfoniopropionate (DMSP) and its catabolite dimethyl sulfide (DMS) are key marine nutrients1,2 that have roles in global sulfur cycling2, atmospheric chemistry3, signalling4,5 and, potentially, climate regulation6,7. The production of DMSP was previously thought to be an oxic and photic process that is mainly confined to the surface oceans. However, here we show that DMSP concentrations and/or rates of DMSP and DMS synthesis are higher in surface sediment from, for example, saltmarsh ponds, estuaries and the deep ocean than in the overlying seawater. A quarter of bacterial strains isolated from saltmarsh sediment produced DMSP (up to 73 mM), and we identified several previously unknown producers of DMSP. Most DMSP-producing isolates contained dsyB8, but some alphaproteobacteria, gammaproteobacteria and actinobacteria used a methionine methylation pathway independent of DsyB that was previously only associated with higher plants. These bacteria contained a methionine methyltransferase gene (mmtN)—a marker for bacterial synthesis of DMSP through this pathway. DMSP-producing bacteria and their dsyB and/or mmtN transcripts were present in all of the tested seawater samples and Tara Oceans bacterioplankton datasets, but were much more abundant in marine surface sediment. Approximately 1 × 108 bacteria g−1 of surface marine sediment are predicted to produce DMSP, and their contribution to this process should be included in future models of global DMSP production. We propose that coastal and marine sediments, which cover a large part of the Earth’s surface, are environments with high levels of DMSP and DMS productivity, and that bacteria are important producers of DMSP and DMS within these environments.
AB - Dimethylsulfoniopropionate (DMSP) and its catabolite dimethyl sulfide (DMS) are key marine nutrients1,2 that have roles in global sulfur cycling2, atmospheric chemistry3, signalling4,5 and, potentially, climate regulation6,7. The production of DMSP was previously thought to be an oxic and photic process that is mainly confined to the surface oceans. However, here we show that DMSP concentrations and/or rates of DMSP and DMS synthesis are higher in surface sediment from, for example, saltmarsh ponds, estuaries and the deep ocean than in the overlying seawater. A quarter of bacterial strains isolated from saltmarsh sediment produced DMSP (up to 73 mM), and we identified several previously unknown producers of DMSP. Most DMSP-producing isolates contained dsyB8, but some alphaproteobacteria, gammaproteobacteria and actinobacteria used a methionine methylation pathway independent of DsyB that was previously only associated with higher plants. These bacteria contained a methionine methyltransferase gene (mmtN)—a marker for bacterial synthesis of DMSP through this pathway. DMSP-producing bacteria and their dsyB and/or mmtN transcripts were present in all of the tested seawater samples and Tara Oceans bacterioplankton datasets, but were much more abundant in marine surface sediment. Approximately 1 × 108 bacteria g−1 of surface marine sediment are predicted to produce DMSP, and their contribution to this process should be included in future models of global DMSP production. We propose that coastal and marine sediments, which cover a large part of the Earth’s surface, are environments with high levels of DMSP and DMS productivity, and that bacteria are important producers of DMSP and DMS within these environments.
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U2 - 10.1038/s41564-019-0527-1
DO - 10.1038/s41564-019-0527-1
M3 - Letter
C2 - 31427729
AN - SCOPUS:85071144869
SN - 2058-5276
VL - 4
SP - 1815
EP - 1825
JO - Nature Microbiology
JF - Nature Microbiology
IS - 11
ER -