• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

调控绿藻莱茵衣藻中 RuBisCO 的积累。

Manipulating RuBisCO accumulation in the green alga, Chlamydomonas reinhardtii.

机构信息

Centre National de la Recherche Scientifique, Unité Mixte de Recherche 7141/Université Pierre et Marie Curie, Institut de Biologie Physico-Chimique, 75005 Paris, France.

出版信息

Plant Mol Biol. 2011 Jul;76(3-5):397-405. doi: 10.1007/s11103-011-9783-z. Epub 2011 May 24.

DOI:10.1007/s11103-011-9783-z
PMID:21607658
Abstract

The nuclear factor, Maturation/stability of RbcL (MRL1), regulates the accumulation of the chloroplast rbcL gene transcript in Chlamydomonas reinhardtii by stabilising the mRNA via its 5' UTR. An absence of MRL1 in algal mrl1 mutants leads to a complete absence of RuBisCO large subunit protein and thus a lack of accumulation of the RuBisCO holoenzyme. By complementing mrl1 mutants by random transformation of the nuclear genome with the MRL1 cDNA, different levels of rbcL transcript accumulate. We also observe that RuBisCO Large Subunit accumulation is perturbed. Complemented strains accumulating as little as 15% RuBisCO protein can grow phototrophically while RuBisCO in this range is limiting for phototrophic growth. We also observe that photosynthetic activity, here measured by the quantum yield of PSII, appears to be a determinant for phototrophic growth. In some strains that accumulate less RuBisCO, a strong production of reactive oxygen species is detected. In the absence of RuBisCO, oxygen possibly acts as the PSI terminal electron acceptor. These results show that random transformation of MRL1 into mrl1 mutants can change RuBisCO accumulation allowing a range of phototrophic growth phenotypes. Furthermore, this technique allows for the isolation of strains with low RuBisCO, within the range of acceptable photosynthetic growth and reasonably low ROS production. MRL1 is thus a potential tool for applications to divert electrons away from photosynthetic carbon metabolism towards alternative pathways.

摘要

核因子,RbcL(MRL1)成熟/稳定因子,通过其 5'UTR 稳定 mRNA 来调节衣藻 rbcL 基因转录本在叶绿体中的积累。藻类 mrl1 突变体中缺乏 MRL1 会导致 RuBisCO 大亚基蛋白完全缺失,从而导致 RuBisCO 全酶积累不足。通过随机转化核基因组并用 MRL1 cDNA 互补 mrl1 突变体,可积累不同水平的 rbcL 转录本。我们还观察到 RuBisCO 大亚基积累受到干扰。积累 RuBisCO 蛋白低至 15%的互补菌株可以进行光合作用生长,而该范围内的 RuBisCO 是光合作用生长的限制因素。我们还观察到光合作用活性,这里通过 PSII 的量子产率来衡量,似乎是光合作用生长的决定因素。在一些积累较少 RuBisCO 的菌株中,检测到强烈的活性氧产生。在没有 RuBisCO 的情况下,氧气可能作为 PSI 末端电子受体。这些结果表明,随机转化 MRL1 到 mrl1 突变体可以改变 RuBisCO 积累,从而允许一系列光合作用生长表型。此外,该技术可用于分离在可接受的光合作用生长范围内、活性氧产生较低且 RuBisCO 水平较低的菌株。因此,MRL1 是一种潜在的工具,可用于将电子从光合碳代谢转移到替代途径。

相似文献

1
Manipulating RuBisCO accumulation in the green alga, Chlamydomonas reinhardtii.调控绿藻莱茵衣藻中 RuBisCO 的积累。
Plant Mol Biol. 2011 Jul;76(3-5):397-405. doi: 10.1007/s11103-011-9783-z. Epub 2011 May 24.
2
MRL1, a conserved Pentatricopeptide repeat protein, is required for stabilization of rbcL mRNA in Chlamydomonas and Arabidopsis.MRL1 是一种保守的五肽重复蛋白,在衣藻和拟南芥中,它对于 rbcL mRNA 的稳定是必需的。
Plant Cell. 2010 Jan;22(1):234-48. doi: 10.1105/tpc.109.066266. Epub 2010 Jan 22.
3
Crystal structure of activated ribulose-1,5-bisphosphate carboxylase/oxygenase from green alga Chlamydomonas reinhardtii complexed with 2-carboxyarabinitol-1,5-bisphosphate.莱茵衣藻中与2-羧基阿拉伯糖醇-1,5-二磷酸复合的活化核酮糖-1,5-二磷酸羧化酶/加氧酶的晶体结构
J Mol Biol. 2002 Feb 22;316(3):679-91. doi: 10.1006/jmbi.2001.5381.
4
Phylogenetic engineering at an interface between large and small subunits imparts land-plant kinetic properties to algal Rubisco.在大亚基和小亚基界面处进行的系统发育工程赋予藻类核酮糖-1,5-二磷酸羧化酶/加氧酶陆地植物的动力学特性。
Proc Natl Acad Sci U S A. 2005 Nov 22;102(47):17225-30. doi: 10.1073/pnas.0508042102. Epub 2005 Nov 10.
5
Accumulation and processing of a recombinant protein designed as a cleavable fusion to the endogenous Rubisco LSU protein in Chlamydomonas chloroplast.衣藻叶绿体中一种设计为与内源性核酮糖-1,5-二磷酸羧化酶/加氧酶大亚基蛋白可裂解融合的重组蛋白的积累与加工。
BMC Biotechnol. 2009 Mar 26;9:26. doi: 10.1186/1472-6750-9-26.
6
Functional hybrid rubisco enzymes with plant small subunits and algal large subunits: engineered rbcS cDNA for expression in chlamydomonas.具有植物小亚基和藻类大亚基的功能杂合 Rubisco 酶:在衣藻中表达的工程化 rbcS cDNA。
J Biol Chem. 2010 Jun 25;285(26):19833-41. doi: 10.1074/jbc.M110.124230. Epub 2010 Apr 27.
7
Pseudoreversion substitution at large-subunit residue 54 influences the CO2/O2 specificity of chloroplast ribulose-bisphosphate carboxylase/oxygenase.大亚基54位残基处的假回复替代影响叶绿体核酮糖-1,5-二磷酸羧化酶/加氧酶的CO₂/O₂特异性。
Plant Physiol. 1995 Oct;109(2):681-5. doi: 10.1104/pp.109.2.681.
8
The BSD2 ortholog in Chlamydomonas reinhardtii is a polysome-associated chaperone that co-migrates on sucrose gradients with the rbcL transcript encoding the Rubisco large subunit.莱茵衣藻中的BSD2直系同源物是一种与多核糖体相关的伴侣蛋白,它在蔗糖梯度上与编码核酮糖-1,5-二磷酸羧化酶大亚基的rbcL转录本共同迁移。
Plant J. 2014 Oct;80(2):345-55. doi: 10.1111/tpj.12638. Epub 2014 Sep 15.
9
RNA binding activity of the ribulose-1,5-bisphosphate carboxylase/oxygenase large subunit from Chlamydomonas reinhardtii.莱茵衣藻1,5-二磷酸核酮糖羧化酶/加氧酶大亚基的RNA结合活性
J Biol Chem. 2004 Mar 12;279(11):10148-56. doi: 10.1074/jbc.M308602200. Epub 2003 Dec 16.
10
RbcS suppressor mutations improve the thermal stability and CO2/O2 specificity of rbcL- mutant ribulose-1,5-bisphosphate carboxylase/oxygenase.RbcS抑制突变提高了rbcL突变型1,5-二磷酸核酮糖羧化酶/加氧酶的热稳定性和二氧化碳/氧气特异性。
Proc Natl Acad Sci U S A. 2000 Dec 19;97(26):14206-11. doi: 10.1073/pnas.260503997.

引用本文的文献

1
Regulation of nucleus-encoded trans-acting factors allows orthogonal fine-tuning of multiple transgenes in the chloroplast of Chlamydomonas reinhardtii.对细胞核编码的反式作用因子的调控能够对莱茵衣藻叶绿体中的多个转基因进行正交微调。
Plant Biotechnol J. 2025 Mar;23(3):1005-1018. doi: 10.1111/pbi.14557. Epub 2024 Dec 28.
2
Singlet-Oxygen-Mediated Regulation of Photosynthesis-Specific Genes: A Role for Reactive Electrophiles in Signal Transduction.单线态氧调控光合作用相关基因:活性亲电物在信号转导中的作用。
Int J Mol Sci. 2024 Aug 2;25(15):8458. doi: 10.3390/ijms25158458.
3
DnaK and DnaJ proteins from Hsp70/40 family are involved in Rubisco biosynthesis in Synechocystis sp. PCC6803 and sustain the enzyme assembly in a heterologous system.

本文引用的文献

1
A novel role for minimal introns: routing mRNAs to the cytosol.内含子最小化的新作用:将 mRNA 导向细胞质。
PLoS One. 2010 Apr 12;5(4):e10144. doi: 10.1371/journal.pone.0010144.
2
Chloroplast RNA metabolism.叶绿体 RNA 代谢。
Annu Rev Plant Biol. 2010;61:125-55. doi: 10.1146/annurev-arplant-042809-112242.
3
MRL1, a conserved Pentatricopeptide repeat protein, is required for stabilization of rbcL mRNA in Chlamydomonas and Arabidopsis.MRL1 是一种保守的五肽重复蛋白,在衣藻和拟南芥中,它对于 rbcL mRNA 的稳定是必需的。
DnaK 和 DnaJ 蛋白来自 Hsp70/40 家族,参与集胞藻 PCC6803 中 Rubisco 的生物合成,并在异源系统中维持该酶的组装。
BMC Plant Biol. 2023 Feb 23;23(1):109. doi: 10.1186/s12870-023-04121-1.
4
Interactions Between Carbon Metabolism and Photosynthetic Electron Transport in a Mutant Without CO Fixation by RuBisCO.在缺乏核酮糖-1,5-二磷酸羧化酶/加氧酶(RuBisCO)固定CO₂功能的突变体中碳代谢与光合电子传递之间的相互作用
Front Plant Sci. 2022 Apr 28;13:876439. doi: 10.3389/fpls.2022.876439. eCollection 2022.
5
Pas de Trois: An Overview of Penta-, Tetra-, and Octo-Tricopeptide Repeat Proteins From and Their Role in Chloroplast Gene Expression.三重奏:来自……的五肽、四肽和八肽重复蛋白概述及其在叶绿体基因表达中的作用
Front Plant Sci. 2021 Nov 17;12:775366. doi: 10.3389/fpls.2021.775366. eCollection 2021.
6
The state of oligomerization of Rubisco controls the rate of synthesis of the Rubisco large subunit in Chlamydomonas reinhardtii.Rubisco 的寡聚状态控制了莱茵衣藻 Rubisco 大亚基的合成速率。
Plant Cell. 2021 Jul 2;33(5):1706-1727. doi: 10.1093/plcell/koab061.
7
Overexpression of Sedoheptulose-1,7-Bisphosphatase Enhances Photosynthesis in and Has No Effect on the Abundance of Other Calvin-Benson Cycle Enzymes.景天庚酮糖-1,7-二磷酸酶的过表达增强了光合作用且对卡尔文-本森循环中其他酶的丰度没有影响。
Front Plant Sci. 2020 Jun 23;11:868. doi: 10.3389/fpls.2020.00868. eCollection 2020.
8
Metabolic Insights Into Infochemicals Induced Colony Formation and Flocculation in Unraveled by Quantitative Proteomics.通过定量蛋白质组学揭示信息化学物质诱导菌落形成和絮凝的代谢机制。
Front Microbiol. 2020 May 7;11:792. doi: 10.3389/fmicb.2020.00792. eCollection 2020.
9
The Mutant Accumulates Proteins Involved in High Light Acclimation.突变体积累参与高光适应的蛋白质。
Plant Physiol. 2019 Dec;181(4):1480-1497. doi: 10.1104/pp.19.01052. Epub 2019 Oct 11.
10
Subcellular Energetics and Carbon Storage in .在 中细胞内能量学和碳储存。
Cells. 2019 Sep 26;8(10):1154. doi: 10.3390/cells8101154.
Plant Cell. 2010 Jan;22(1):234-48. doi: 10.1105/tpc.109.066266. Epub 2010 Jan 22.
4
A new setup for in vivo fluorescence imaging of photosynthetic activity.一种用于活体荧光成像的新设置。
Photosynth Res. 2009 Oct;102(1):85-93. doi: 10.1007/s11120-009-9487-2. Epub 2009 Aug 21.
5
Redox and ATP control of photosynthetic cyclic electron flow in Chlamydomonas reinhardtii (I) aerobic conditions.莱茵衣藻光合循环电子流的氧化还原与ATP调控(I)需氧条件
Biochim Biophys Acta. 2010 Jan;1797(1):44-51. doi: 10.1016/j.bbabio.2009.07.009. Epub 2009 Aug 3.
6
Chloroplast protein targeting involves localized translation in Chlamydomonas.叶绿体蛋白靶向涉及衣藻中的局部翻译。
Proc Natl Acad Sci U S A. 2009 Feb 3;106(5):1439-44. doi: 10.1073/pnas.0811268106. Epub 2009 Jan 21.
7
Strategies to facilitate transgene expression in Chlamydomonas reinhardtii.促进莱茵衣藻中转基因表达的策略。
Planta. 2009 Mar;229(4):873-83. doi: 10.1007/s00425-008-0879-x. Epub 2009 Jan 7.
8
Molecular identification and function of cis- and trans-acting determinants for petA transcript stability in Chlamydomonas reinhardtii chloroplasts.莱茵衣藻叶绿体中petA转录本稳定性的顺式和反式作用决定因素的分子鉴定及功能
Mol Cell Biol. 2008 Sep;28(17):5529-42. doi: 10.1128/MCB.02056-07. Epub 2008 Jun 23.
9
Translational control of photosynthetic gene expression in phototrophic eukaryotes.光合自养真核生物中光合基因表达的翻译控制
Physiol Plant. 2008 Jul;133(3):507-15. doi: 10.1111/j.1399-3054.2008.01091.x. Epub 2008 Jul 1.
10
Synthesis of the D2 protein of photosystem II in Chlamydomonas is controlled by a high molecular mass complex containing the RNA stabilization factor Nac2 and the translational activator RBP40.衣藻光系统II的D2蛋白的合成受一种高分子量复合物控制,该复合物包含RNA稳定因子Nac2和翻译激活因子RBP40。
Plant Cell. 2007 Nov;19(11):3627-39. doi: 10.1105/tpc.107.051722. Epub 2007 Nov 30.