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Biogenic production of DMSP and its degradation to DMS—their roles in the global sulfur cycle

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【作者】 Xiao-Hua ZhangJi LiuJingli LiuGuipeng YangChun-Xu XueAndrew R.J.CursonJonathan D.Todd

【Author】 Xiao-Hua Zhang;Ji Liu;Jingli Liu;Guipeng Yang;Chun-Xu Xue;Andrew R.J.Curson;Jonathan D.Todd;MOE Key Laboratory of Marine Genetics and Breeding, College of Marine Life Sciences, Ocean University of China;Laboratory for Marine Ecology and Environmental Science, Qingdao National Laboratory for Marine Science and Technology;College of Chemistry and Chemical Engineering, Ocean University of China;School of Biological Sciences, University of East Anglia;

【通讯作者】 Xiao-Hua Zhang;

【机构】 MOE Key Laboratory of Marine Genetics and Breeding, College of Marine Life Sciences, Ocean University of ChinaLaboratory for Marine Ecology and Environmental Science, Qingdao National Laboratory for Marine Science and TechnologyCollege of Chemistry and Chemical Engineering, Ocean University of ChinaSchool of Biological Sciences, University of East Anglia

【摘要】 Dimethyl sulfide(DMS) is the most abundant form of volatile sulfur in Earth’s oceans, and is mainly produced by the enzymatic clevage of dimethylsulfoniopropionate(DMSP). DMS and DMSP play important roles in driving the global sulfur cycle and may affect climate. DMSP is proposed to serve as an osmolyte, a grazing deterrent, a signaling molecule, an antioxidant, a cryoprotectant and/or as a sink for excess sulfur. It was long believed that only marine eukaryotes such as phytoplankton produce DMSP. However, we recently discovered that marine heterotrophic bacteria can also produce DMSP, making them a potentially important source of DMSP. At present, one prokaryotic and two eukaryotic DMSP synthesis enzymes have been identified.Marine heterotrophic bacteria are likely the major degraders of DMSP, using two known pathways: demethylation and cleavage.Many phytoplankton and some fungi can also cleave DMSP. So far seven different prokaryotic and one eukaryotic DMSP lyases have been identified. This review describes the global distribution pattern of DMSP and DMS, the known genes for biosynthesis and cleavage of DMSP, and the physiological and ecological functions of these important organosulfur molecules, which will improve understanding of the mechanisms of DMSP and DMS production and their roles in the environment.

【Abstract】 Dimethyl sulfide(DMS) is the most abundant form of volatile sulfur in Earth’s oceans, and is mainly produced by the enzymatic clevage of dimethylsulfoniopropionate(DMSP). DMS and DMSP play important roles in driving the global sulfur cycle and may affect climate. DMSP is proposed to serve as an osmolyte, a grazing deterrent, a signaling molecule, an antioxidant, a cryoprotectant and/or as a sink for excess sulfur. It was long believed that only marine eukaryotes such as phytoplankton produce DMSP. However, we recently discovered that marine heterotrophic bacteria can also produce DMSP, making them a potentially important source of DMSP. At present, one prokaryotic and two eukaryotic DMSP synthesis enzymes have been identified.Marine heterotrophic bacteria are likely the major degraders of DMSP, using two known pathways: demethylation and cleavage.Many phytoplankton and some fungi can also cleave DMSP. So far seven different prokaryotic and one eukaryotic DMSP lyases have been identified. This review describes the global distribution pattern of DMSP and DMS, the known genes for biosynthesis and cleavage of DMSP, and the physiological and ecological functions of these important organosulfur molecules, which will improve understanding of the mechanisms of DMSP and DMS production and their roles in the environment.

【基金】 supported by the National Natural Science Foundation of China (91751202 and 41730530);the National Key Research and Development Program of China (2016YFA0601303 and 2018YFC0310701);the Marine S&T Fund of Shandong Province for Pilot National Laboratory for Marine Science and Technology (Qingdao) (2018SDKJ0406-4);Natural Environmental Research Council grants (NE/ N002385, NE/P012671 and NE/S001352) fund ARJC and JDT
  • 【文献出处】 Science China(Life Sciences) ,中国科学:生命科学(英文版) , 编辑部邮箱 ,2019年10期
  • 【分类号】Q14
  • 【网络出版时间】2019-06-24 14:03
  • 【被引频次】10
  • 【下载频次】55
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