Light/Shade Adaptation of Prochlorothrix Hollandica
荷兰原绿丝菌的光/荫适应
基本信息
- 批准号:9204672
- 负责人:
- 金额:$ 15.3万
- 依托单位:
- 依托单位国家:美国
- 项目类别:Standard Grant
- 财政年份:1992
- 资助国家:美国
- 起止时间:1992-09-01 至 1995-08-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The rationale for this work is based on the fact that all photosynthetic organisms must adapt to changes in environment light intensity in order to maximize photosynthetic efficiency. At high light, excess energy has to be dissipated to prevent photodamage, while at low light, photon capture has be maximized to allow photosynthesis to proceed efficiently. We have been studying the photosynthetic prokaryote, Prochlorothrix hollandica, as a model system to examine the light/shade adaptation of the photosynthetic apparatus. This bacterium is well-suited to these studies because it is structurally similar to higher plant chloroplasts, but can be manipulated in the lab more easily that higher plants or eukaryotic algae. Our work has characterized the events occurring during light/shade adaptation in both P. hollandica and plant chloroplasts, and we have shown that similar mechanisms occur in both systems. Overall, we believe that analyzing this process in P. hollandica will reveal in more detail the pathway required for plants to handle alterations in environmental light intensity. %%% Specifically, our work has shown that light/shade adaptation involves in part the interplay of two separate events. First, upon a shift to high light, the overall chlorophyll pigment system becomes reorganized in approximately 30 minutes; we calculate 40% of the accessory chlorophyll pigments are capable of changing their orientation such that energy capture and transfer is altered at high light. This mechanism appears to be controlled by a light-activated protein kinase. Second, as cells experience high light for several hours, a light-activated metalloprotease activity degrades a subset of the accessory chlorophyll-binding proteins. The function of this protease is probably to limit the amount of photon capture at high irradiances. Understanding precisely the mechanism(s) by which cells sense high light and trigger these responses will help us understand how photosynthesis is regulated in chloroplast (plant) systems. To date, we have cloned many of the genes encoding the components involved in these mechanisms; these include the genes encoding the protein kinase. We are currently examining how light affects the expression of these genes, and how the function of the kinase affects the function and organization of the photosynthetic light-harvesting antenna. Lastly, we are examining in detail how the proteolytic activity acts to destroy the accessory chlorophyll-proteins in high light; it is possible that the accessory chlorophyll-proteins are targeted for proteolysis by their phosphorylation by the thylakoid protein kinase.
这项工作的理由是, 光合生物必须适应环境的变化 光强度,以最大限度地提高光合效率。 在强光下,多余的能量必须消散,以防止 光损伤,而在低光下,光子捕获已被最大化 使光合作用有效进行。 我们一直 研究光合原核生物原绿丝菌 hollandica,作为一个模型系统来检查光/影 光合机构的适应。 这种细菌 非常适合这些研究,因为它在结构上类似于 高等植物叶绿体,但可以在实验室中操作, 比高等植物或真核藻类更容易。 我们的工作 描述了在光/影适应过程中发生的事件 在P.hollandica和植物叶绿体中,我们已经证明 两个系统都有类似的机制。 总的来说,我们 我相信,分析P. hollandica的这一过程将揭示 更详细地描述了植物处理 环境光强度的变化。 %%% 具体来说,我们的工作表明,光/影适应 部分涉及两个独立事件的相互作用。 第一、 当转向强光时, 系统在大约30分钟内进行重组;我们 计算出40%的辅助叶绿素 改变它们的方向, 转移在强光下改变。 这种机制似乎是 由光激活蛋白激酶控制。 第二,作为细胞 经历强光几个小时,光激活 金属蛋白酶活性降解附件的子集 叶绿素结合蛋白 这种蛋白酶的功能是 很可能是为了限制在高温下的光子捕获量, 辐照度 准确理解 细胞感知强光并触发这些反应将帮助我们 了解光合作用是如何在叶绿体(植物)中调节的 系统. 到目前为止,我们已经克隆了许多编码 参与这些机制的成分;这些包括基因 编码蛋白激酶。 我们目前正在研究如何 光会影响这些基因的表达, 激酶的功能和组织的影响, 光合集光天线。 最后,我们 详细研究蛋白水解活性如何破坏 辅助叶绿素蛋白在强光下;这是可能的 辅助叶绿素蛋白是 通过类囊体蛋白磷酸化的蛋白水解 激酶。
项目成果
期刊论文数量(0)
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George Bullerjahn其他文献
Increasing mercury bioaccumulation and biomagnification rates of Nile perch (emLates niloticus/em L.) in Winam Gulf, Lake Victoria, Kenya
肯尼亚维多利亚湖威纳姆湾尼罗河鲈鱼(Lates niloticus L.)汞生物累积和生物放大率的增加
- DOI:
10.1016/j.scitotenv.2024.170059 - 发表时间:
2024-03-15 - 期刊:
- 影响因子:8.000
- 作者:
Ken G. Drouillard;Linda Campbell;Dennis Otieno;James Achiya;Albert Getabu;Job Mwamburi;Lewis Sitoki;Reuben Omondi;Anakalo Shitandi;Bethwell Owuor;James Njiru;George Bullerjahn;R. Michael Mckay;Kefa M. Otiso;Emma Tebbs;Katelyn Barker;Max Beal;Katelyn Brown;Aidan Byrne;Linet I. Kiteresi;Brittany Zepernick - 通讯作者:
Brittany Zepernick
Regulation of cyanobacterial pigment-protein composition and organization by environmental factors
- DOI:
10.1007/bf00042982 - 发表时间:
1988-10-01 - 期刊:
- 影响因子:3.700
- 作者:
Harold Riethman;George Bullerjahn;K. J. Reddy;Louis A. Sherman - 通讯作者:
Louis A. Sherman
George Bullerjahn的其他文献
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{{ truncateString('George Bullerjahn', 18)}}的其他基金
IRES Track II: Advanced studies institute on water quality and harmful algal blooms in Lake Victoria
IRES Track II:维多利亚湖水质和有害藻华高级研究机构
- 批准号:
1953468 - 财政年份:2020
- 资助金额:
$ 15.3万 - 项目类别:
Standard Grant
Lake Erie Center for Fresh Waters and Human Health
伊利湖淡水与人类健康中心
- 批准号:
1840715 - 财政年份:2018
- 资助金额:
$ 15.3万 - 项目类别:
Continuing Grant
Workshop: "Global Solutions to Regional Problems: Collecting Global Expertise to the Problem of Harmful Algal Blooms" at Bowling Green State University, Ohio on April 13-14, 2015
研讨会:“区域问题的全球解决方案:收集有害藻华问题的全球专业知识”,俄亥俄州鲍灵格林州立大学,2015 年 4 月 13 日至 14 日
- 批准号:
1515671 - 财政年份:2015
- 资助金额:
$ 15.3万 - 项目类别:
Standard Grant
"LiT": Regulation of 5-Aminolevulinic Acid Biosynthesis in the Bacterium Rhodobacter sphaeroides
“LiT”:球形红杆菌中 5-氨基乙酰丙酸生物合成的调节
- 批准号:
0921449 - 财政年份:2009
- 资助金额:
$ 15.3万 - 项目类别:
Standard Grant
Conference: Support for the 8th Cyanobacterial Molecular Biology Workshop to be held in St. Adele, Quebec on August 25-29, 2004
会议:支持将于2004年8月25日至29日在魁北克省圣阿黛尔举行的第八届蓝藻分子生物学研讨会
- 批准号:
0413569 - 财政年份:2004
- 资助金额:
$ 15.3万 - 项目类别:
Standard Grant
Acquisition of Molecular Imaging and Plate Reading Systems
获取分子成像和读板系统
- 批准号:
0070334 - 财政年份:2000
- 资助金额:
$ 15.3万 - 项目类别:
Standard Grant
Analysis of a Stress-Inducible DNA-Binding Protein in a Cyanobacterium
蓝藻中应激诱导 DNA 结合蛋白的分析
- 批准号:
9634049 - 财政年份:1996
- 资助金额:
$ 15.3万 - 项目类别:
Standard Grant
Structure and Function of the Prochlorothrix Hollandica Photosynthetic Antenna System
荷兰原绿丝菌光合天线系统的结构与功能
- 批准号:
8903060 - 财政年份:1989
- 资助金额:
$ 15.3万 - 项目类别:
Continuing Grant
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