A novel pathway for the production of the climate cooling gas dimethyl sulfide - how important is the mddA gene to global DMS emissions?
A novel pathway for the production of the climate cooling gas dimethyl sulfide - how important is the mddA gene to global DMS emissions?
批准号:
NE/M004449/1
负责人:
Jonathan Todd
金额:
$47.51万
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2014
资助国家:
英国
项目状态:
已结题
起止时间:
2014 至 --
中文摘要
“海边的味道”实际上是由微生物产生的一种叫做二甲基硫化物(DMS)的气体化合物引起的。这种气体很重要,因为它是一种非常丰富的有机硫化合物,从海洋环境中释放到空气中。全球每年大约生产3亿吨DMS,主要是通过细菌生产的。此外,DMS氧化产生的化学产物有助于在海洋上空形成云,在一定程度上影响到达地球表面的阳光,对气候产生影响。然后,这些产品以雨的形式返回地球,代表了全球硫循环的关键组成部分。有趣的是,DMS对包括海鸟、甲壳类动物和海洋哺乳动物在内的许多生物都是一种有效的化学引诱剂,因为它们将DMS与食物联系在一起,所以都向DMS移动。目前,人们普遍认为DMS主要是由微生物降解渗透物二甲基磺酰丙酸(DMSP)产生的,而DMSP是由海洋中的浮游植物、海藻和少数耐盐植物产生的。我们和罗恩·基恩的初步工作促使我们质疑是否仅仅是这些过程产生了DMS。在我们的初步数据中,我们有:1;发现了一种微生物途径,甲烷硫醇依赖性DMS生产(Mdd)途径,该途径产生DMS,但不涉及DMSP。2. 展示了“欺骗假单胞菌”如何通过一种名为mdda的基因制造DMS。研究表明,该基因存在于广泛的细菌中,如大豆的固氮共生体日本慢根瘤菌、结核病的病原体结核分枝杆菌和一些蓝藻。4. 表明Mdd途径在咸水和淡水沉积物中均有活性,并且mddA基因在海洋沉积物细菌中含量丰富。表明其他细菌有其他未被发现的从甲硫醇中制造DMS的方法。我们希望研究这种新的DMS生产途径对这种气候变化气体的全球生产有多重要。为了回答这个问题,我们将对各种海洋和淡水环境进行采样,并研究Mdd途径在这些环境中的活跃程度,以及这种产生DMS的新途径是如何被调节的。我们已经知道,这种Mdd途径可能在我们的大多数样本地点都很活跃,包括来自盐沼、淡水湖、泥炭沼泽和海水的泥浆。同样重要的是要知道哪些微生物负责这一过程(由Mdd介导)以及它们为什么产生DMS。我们将使用一套强大的微生物生态学技术,结合遗传工具来识别微生物和通过这种新的Mdd途径产生DMS的关键基因。我们将确定:a)生活在有氧和无氧泥浆样品以及海水中的微生物;b)当我们通过Mdd途径增加DMS产量时,这些微生物群落是如何变化的;c)在这些不同的环境中,mddA基因的哪种形式(以及该基因编码的酶)负责高DMS产量。为了了解环境中的细菌如何以及为什么具有Mdd活性,我们将详细研究一些模式细菌,其中一些已经从我们的样品中分离出来。这将涉及识别和突变编码Mdd途径的基因,以确定它们为什么使用它。这将在具有特定基因“mddA”的细菌上进行,但也可以在那些没有mddA的细菌上进行,这将使我们能够识别新的mdd基因。考虑到气候活性气体DMS的环境后果,了解哪些类型的微生物影响其生产以及涉及哪些潜在途径是很重要的。这将帮助我们在未来建立环境变化如何影响这些气候过程平衡的模型。
英文摘要
The "smell of the seaside" is actually caused by a gaseous compound called dimethyl sulfide (DMS) that is produced by microbes. This gas is important because it is a very abundant organic sulfur compound which is released to the air from the marine environment. Globally, approximately 300 million tons of DMS per annum is produced, mainly by bacteria. Also, chemical products arising from DMS oxidation help form clouds over the oceans, to an extent that affects the sunlight reaching the Earth's surface, with effects on climate. In turn, these products are delivered back to Earth as rain, representing a key component of the global sulfur cycle. Interestingly, DMS is a potent chemo-attractant for many organisms including seabirds, crustaceans and marine mammals that all move towards DMS because they associate DMS with food.Currently it is widely accepted that DMS is mainly produced as a result of microbes degrading the osmolyte dimethylsulfoniopropionate (DMSP), which is produced by phytoplankton in the oceans, by seaweeds and by a few salt-tolerant plants. Our preliminary work and that of Ron Kiene, has prompted us to question whether it is solely these processes that produce DMS.In our preliminary data we have:1. Found a microbial pathway, the methanethiol-dependent DMS production (Mdd) pathway, that produces DMS but which does not involve DMSP. 2. Shown how the bacterium "Pseudomonas deceptionensis" makes DMS via a gene called mddA.3. Shown that this gene is found in a wide range of bacteria such as Bradyrhizobium japonicum, a nitrogen-fixing symbiont of soybeans, Mycobacterium tuberculosis, the causative agent of tuberculosis and some cyanobacteria. 4. Shown that the Mdd pathway is active in both salty and freshwater sediments and that the mddA gene is abundant in bacteria living in marine sediments.5. Shown that other bacteria have other undiscovered ways of making DMS from methanethiol.We wish to investigate how important this novel DMS production pathway is for the global production of this climate changing gas. To answer this question, we will sample various marine and freshwater environments and investigate how active the Mdd pathway is in these environments and how this novel pathway for the production of DMS is regulated. We already know that this Mdd pathway is probably active in most of our sample sites, which include mud from a saltmarsh, a freshwater lake, a peat bog and seawater. It is equally important to know which microbes are responsible for the process (mediated by Mdd) and why they produce DMS. We will use a powerful suite of microbial ecology techniques, combined with genetic tools to identify the microbes and the key genes involved in producing DMS via this new Mdd pathway.We will identify: a) the microbes living in both the oxic and anoxic mud samples and in seawater; b) how these microbial communities change when we enrich for increased DMS production via the Mdd pathway and c) which forms of the mddA gene (and the enzyme encoded by this gene) are responsible for high DMS production in these varied environments. To understand how and why bacteria in the environment are Mdd active, we will study in detail a few model bacteria, some of which have been isolated from our sample sites. This will involve identifying and mutating the genes encoding the Mdd pathway to ascertain why they use it. This will be done with bacteria that have a specific gene "mddA", but, also on those that do not, which will allow us to identify new mdd genes. Given the environmental consequences of the climate-active gas DMS, it is important to know which types of microbes affect its production and which of the various potential pathways are involved. This will help us in the future to model how changes in the environment impact on the balance of these climate processes.
期刊论文(10)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1038/ismej.2017.105
发表时间:
2017-10
期刊:
The ISME journal
影响因子:
--
作者:
[Carrión O, Pratscher J, Curson ARJ, Williams BT, Rostant WG, Murrell JC, Todd JD]
通讯作者:
Todd JD
DOI:
10.1371/journal.pone.0127288
发表时间:
2015
期刊:
PloS one
影响因子:
3.7
作者:
[Brummett AE, Schnicker NJ, Crider A, Todd JD, Dey M]
通讯作者:
Dey M
DOI:
10.1038/ismej.2017.148
发表时间:
2018-01
期刊:
The ISME journal
影响因子:
--
作者:
[Eyice Ö, Myronova N, Pol A, Carrión O, Todd JD, Smith TJ, Gurman SJ, Cuthbertson A, Mazard S, Mennink-Kersten MA, Bugg TD, Andersson KK, Johnston AW, Op den Camp HJ, Schäfer H]
通讯作者:
Schäfer H
DiMethylSulfonioPropionate cycling In Terrestrial environments (DMSP InTerrest)
-
批准号:NE/X000990/1
-
项目类别:Research Grant
-
资助金额:$64.26万
-
财政年份:2023
-
负责人:Jonathan Todd
-
依托单位:
Organosulfur cycling in abundant anoxic marine sediments: a case study of saltmarsh sediments
-
批准号:NE/S001352/1
-
项目类别:Research Grant
-
资助金额:$53.69万
-
财政年份:2018
-
负责人:Jonathan Todd
-
依托单位:
A multidisciplinary study of DMSP production and lysis - from enzymes to organisms to process modelling.
-
批准号:NE/P012671/1
-
项目类别:Research Grant
-
资助金额:$56.24万
-
财政年份:2017
-
负责人:Jonathan Todd
-
依托单位:
Bacteria make DMSP - how significant is this process?
-
批准号:NE/N002385/1
-
项目类别:Research Grant
-
资助金额:$46.17万
-
财政年份:2016
-
负责人:Jonathan Todd
-
依托单位:
How do eukaryotic phytoplankton produce the most abundant organo-sulphur compound in the world's oceans?
-
批准号:NE/J01138X/1
-
项目类别:Research Grant
-
资助金额:$50.68万
-
财政年份:2012
-
负责人:Jonathan Todd
-
依托单位:
国内基金
海外基金
登录
查看更多内容
Foxc2介导Syap1/Akt信号通路调控破骨/成骨细胞分化促进颞下颌关节骨关节炎的机制研究
-
批准号:82370979
-
项目类别:面上项目
-
资助金额:48.00万元
-
批准年份:2023
-
负责人:张善勇
-
依托单位:
肠道菌群介导的脱氧胆酸激活S1PR2/NLRP3/IL-1β通路在炎症性肠病合并艰难梭菌感染中的致病机制研究
-
批准号:82372306
-
项目类别:面上项目
-
资助金额:48.00万元
-
批准年份:2023
-
负责人:彭奕冰
-
依托单位:
PROCR信号通路介导的血管新生在卵巢组织移植中的作用及机制研究
-
批准号:82371726
-
项目类别:面上项目
-
资助金额:50.00万元
-
批准年份:2023
-
负责人:李文
-
依托单位:
GREB1突变介导雌激素受体信号通路导致深部浸润型子宫内膜异位症的分子遗传机制研究
-
批准号:82371652
-
项目类别:面上项目
-
资助金额:45.00万元
-
批准年份:2023
-
负责人:刘开江
-
依托单位:
cGAS-STING通路调控单核细胞活化参与Graves病发病的机制研究
-
批准号:82370787
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:王曙
-
依托单位:
基于压力敏感肾单位微流控芯片的肾上皮细胞CAT1-mTOR通路在梗阻性肾损伤中的作用机制研究
-
批准号:82370678
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:林厚维
-
依托单位:
GASP-1通过Myostatin信号通路调控颏舌肌功能的作用及机制研究
-
批准号:82371131
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:易红良
-
依托单位:
运用3D打印和生物反应器构建仿生尿道模型探索Hippo-YAP信号通路调控尿道损伤修复的机制研究
-
批准号:82370684
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:傅强
-
依托单位:
“肠—肝轴”PPARα/CYP8B1胆汁酸合成信号通路在减重手术改善糖脂代谢中的作用与机制
-
批准号:82370902
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:田景琰
-
依托单位:
紧密连接蛋白PARD3下调介导黏膜上皮屏障破坏激活STAT3/SNAI2通路促进口腔白斑病形成及进展的机制研究
-
批准号:82370954
-
项目类别:面上项目
-
资助金额:47.00万元
-
批准年份:2023
-
负责人:沈雪敏
-
依托单位: