• 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

果胶生物合成:拟南芥中的 GALS1 是一种β-1,4-半乳糖基-β-1,4-半乳糖基转移酶。

Pectin biosynthesis: GALS1 in Arabidopsis thaliana is a β-1,4-galactan β-1,4-galactosyltransferase.

机构信息

Feedstocks Division, Joint BioEnergy Institute, Emeryville, California 94608, USA.

出版信息

Plant Cell. 2012 Dec;24(12):5024-36. doi: 10.1105/tpc.112.106625. Epub 2012 Dec 14.

DOI:10.1105/tpc.112.106625
PMID:23243126
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3556973/
Abstract

β-1,4-Galactans are abundant polysaccharides in plant cell walls, which are generally found as side chains of rhamnogalacturonan I. Rhamnogalacturonan I is a major component of pectin with a backbone of alternating rhamnose and galacturonic acid residues and side chains that include α-1,5-arabinans, β-1,4-galactans, and arabinogalactans. Many enzymes are required to synthesize pectin, but few have been identified. Pectin is most abundant in primary walls of expanding cells, but β-1,4-galactan is relatively abundant in secondary walls, especially in tension wood that forms in response to mechanical stress. We investigated enzymes in glycosyltransferase family GT92, which has three members in Arabidopsis thaliana, which we designated GALACTAN SYNTHASE1, (GALS1), GALS2 and GALS3. Loss-of-function mutants in the corresponding genes had a decreased β-1,4-galactan content, and overexpression of GALS1 resulted in plants with 50% higher β-1,4-galactan content. The plants did not have an obvious growth phenotype. Heterologously expressed and affinity-purified GALS1 could transfer Gal residues from UDP-Gal onto β-1,4-galactopentaose. GALS1 specifically formed β-1,4-galactosyl linkages and could add successive β-1,4-galactosyl residues to the acceptor. These observations confirm the identity of the GT92 enzyme as β-1,4-galactan synthase. The identification of this enzyme could provide an important tool for engineering plants with improved bioenergy properties.

摘要

β-1,4-半乳糖聚糖是植物细胞壁中丰富的多糖,通常作为鼠李半乳糖醛酸 I 型果胶的侧链存在。鼠李半乳糖醛酸 I 型果胶是果胶的主要成分,其主链由交替的鼠李糖和半乳糖醛酸残基组成,侧链包括α-1,5-阿拉伯聚糖、β-1,4-半乳糖聚糖和阿拉伯半乳聚糖。合成果胶需要多种酶,但已鉴定出的酶很少。果胶在扩张细胞的初生壁中含量最丰富,但β-1,4-半乳糖聚糖在次生壁中相对丰富,特别是在应对机械压力形成的紧张木中。我们研究了糖基转移酶家族 GT92 中的酶,该家族在拟南芥中有三个成员,我们将其命名为半乳糖聚糖合酶 1(GALS1)、GALS2 和 GALS3。相应基因的功能丧失突变体β-1,4-半乳糖聚糖含量降低,过表达 GALS1 导致β-1,4-半乳糖聚糖含量增加 50%。这些植物没有明显的生长表型。异源表达和亲和纯化的 GALS1 可以将 Gal 残基从 UDP-Gal 转移到β-1,4-半乳糖五糖上。GALS1 特异性形成β-1,4-半乳糖糖苷键,并可以将连续的β-1,4-半乳糖基残基添加到受体上。这些观察结果证实了 GT92 酶作为β-1,4-半乳糖聚糖合酶的身份。该酶的鉴定为工程植物提供了具有改善的生物能源特性的重要工具。

相似文献

1
Pectin biosynthesis: GALS1 in Arabidopsis thaliana is a β-1,4-galactan β-1,4-galactosyltransferase.果胶生物合成:拟南芥中的 GALS1 是一种β-1,4-半乳糖基-β-1,4-半乳糖基转移酶。
Plant Cell. 2012 Dec;24(12):5024-36. doi: 10.1105/tpc.112.106625. Epub 2012 Dec 14.
2
The Three Members of the Arabidopsis Glycosyltransferase Family 92 are Functional β-1,4-Galactan Synthases.拟南芥糖基转移酶家族 92 的三个成员是功能性的β-1,4-半乳糖基转移酶。
Plant Cell Physiol. 2018 Dec 1;59(12):2624-2636. doi: 10.1093/pcp/pcy180.
3
Cell wall β-1,4-galactan regulated by the BPC1/BPC2-GALS1 module aggravates salt sensitivity in Arabidopsis thaliana.BPC1/BPC2-GALS1 模块调控的细胞壁 β-1,4-半乳糖聚糖加剧拟南芥的盐敏感性。
Mol Plant. 2021 Mar 1;14(3):411-425. doi: 10.1016/j.molp.2020.11.023. Epub 2020 Dec 1.
4
Bifunctional glycosyltransferases catalyze both extension and termination of pectic galactan oligosaccharides.双功能糖基转移酶催化果胶半乳糖醛酸寡糖的延伸和终止。
Plant J. 2018 Apr;94(2):340-351. doi: 10.1111/tpj.13860. Epub 2018 Mar 22.
5
A gene stacking approach leads to engineered plants with highly increased galactan levels in Arabidopsis.一种基因叠加方法可培育出拟南芥中半乳聚糖水平大幅提高的工程植物。
BMC Plant Biol. 2014 Dec 10;14:344. doi: 10.1186/s12870-014-0344-x.
6
The salt-activated CBF1/CBF2/CBF3-GALS1 module fine-tunes galactan-induced salt hypersensitivity in Arabidopsis.盐激活的 CBF1/CBF2/CBF3-GALS1 模块精细调控拟南芥中半乳聚糖诱导的耐盐性。
J Integr Plant Biol. 2023 Aug;65(8):1904-1917. doi: 10.1111/jipb.13501. Epub 2023 Jul 4.
7
Structural changes in cell wall pectic polymers contribute to freezing tolerance induced by cold acclimation in plants.细胞壁果胶聚合物的结构变化有助于植物通过冷驯化诱导产生抗冻性。
Curr Biol. 2024 Mar 11;34(5):958-968.e5. doi: 10.1016/j.cub.2024.01.045. Epub 2024 Feb 8.
8
A DUF-246 family glycosyltransferase-like gene affects male fertility and the biosynthesis of pectic arabinogalactans.一个DUF-246家族类糖基转移酶基因影响雄性育性和果胶阿拉伯半乳聚糖的生物合成。
BMC Plant Biol. 2016 Apr 18;16:90. doi: 10.1186/s12870-016-0780-x.
9
Structural and biochemical insight into a modular β-1,4-galactan synthase in plants.植物中模块化 β-1,4-半乳糖基转移酶的结构和生化见解。
Nat Plants. 2023 Mar;9(3):486-500. doi: 10.1038/s41477-023-01358-4. Epub 2023 Feb 27.
10
Galactosyltransferases from Arabidopsis thaliana in the biosynthesis of type II arabinogalactan: molecular interaction enhances enzyme activity.拟南芥中的半乳糖基转移酶在II型阿拉伯半乳聚糖生物合成中的作用:分子相互作用增强酶活性
BMC Plant Biol. 2014 Apr 3;14:90. doi: 10.1186/1471-2229-14-90.

引用本文的文献

1
Cell wall-related glycosyltransferases and wall architecture in the model liverwort Marchantia polymorpha.模式苔藓植物多歧苏铁细胞壁相关糖基转移酶与细胞壁结构
Plant J. 2025 Sep;123(5):e70439. doi: 10.1111/tpj.70439.
2
Galactan mobilization during carbon starvation compromises plant cell wall-mediated resistance to fungal infection.碳饥饿期间半乳聚糖的动员损害了植物细胞壁介导的对真菌感染的抗性。
Plant J. 2025 Aug;123(4):e70438. doi: 10.1111/tpj.70438.
3
CSLD5-mediated cell wall remodelling regulates tissue mechanics and shoot meristem growth.CSLD5介导的细胞壁重塑调节组织力学和茎尖分生组织生长。
Nat Commun. 2025 Aug 6;16(1):7229. doi: 10.1038/s41467-025-62651-8.
4
How it all begins: molecular players of the early graviresponse in the non-elongating part of flax stem.一切如何开始:亚麻茎非伸长部分早期重力反应的分子参与者。
Plant Mol Biol. 2025 Apr 26;115(3):61. doi: 10.1007/s11103-025-01588-4.
5
Synthetic-biology approach for plant lignocellulose engineering.用于植物木质纤维素工程的合成生物学方法。
Plant Biotechnol (Tokyo). 2024 Sep 25;41(3):213-230. doi: 10.5511/plantbiotechnology.24.0630a.
6
A Fresh Look at Celery Collenchyma and Parenchyma Cell Walls Through a Combination of Biochemical, Histochemical, and Transcriptomic Analyses.通过生物化学、组织化学和转录组学分析相结合重新审视芹菜厚角组织和薄壁组织细胞壁
Int J Mol Sci. 2025 Jan 16;26(2):738. doi: 10.3390/ijms26020738.
7
Environmental gradients shape genetic variation in the desert moss, Syntrichia caninervis Mitt. (Pottiaceae).环境梯度塑造了沙漠苔藓犬齿藓(Syntrichia caninervis Mitt.,丛藓科)的遗传变异。
Sci Rep. 2025 Jan 15;15(1):2064. doi: 10.1038/s41598-025-86305-3.
8
Daily glycome and transcriptome profiling reveals polysaccharide structures and correlated glycosyltransferases critical for cotton fiber growth.每日糖组和转录组分析揭示了对棉纤维生长至关重要的多糖结构和相关糖基转移酶。
Plant J. 2024 Dec;120(5):1857-1879. doi: 10.1111/tpj.17084. Epub 2024 Oct 23.
9
Antagonistic functions of CTL1 and SUH1 mediate cell wall assembly in .CTL1和SUH1的拮抗功能介导了……中的细胞壁组装。 (原文中“in”后面缺少具体内容)
Plant Direct. 2024 Mar 23;8(3):e580. doi: 10.1002/pld3.580. eCollection 2024 Mar.
10
The plant cell wall-dynamic, strong, and adaptable-is a natural shapeshifter.植物细胞壁——动态、坚固且适应性强——是一种天然的变形金刚。
Plant Cell. 2024 May 1;36(5):1257-1311. doi: 10.1093/plcell/koad325.

本文引用的文献

1
The polysaccharide structure of potato cell walls: Chemical fractionation.马铃薯细胞壁多糖结构:化学分级分离。
Planta. 1981 Jun;152(2):93-100. doi: 10.1007/BF00391179.
2
Three members of the Arabidopsis glycosyltransferase family 8 are xylan glucuronosyltransferases.拟南芥糖基转移酶家族 8 的三个成员是木聚糖葡萄糖醛酸基转移酶。
Plant Physiol. 2012 Aug;159(4):1408-17. doi: 10.1104/pp.112.200964. Epub 2012 Jun 15.
3
Plant Glycosyltransferases Beyond CAZy: A Perspective on DUF Families.植物糖基转移酶超越 CAZy:DUF 家族的视角。
Front Plant Sci. 2012 Mar 28;3:59. doi: 10.3389/fpls.2012.00059. eCollection 2012.
4
Isolation and proteomic characterization of the Arabidopsis Golgi defines functional and novel components involved in plant cell wall biosynthesis.拟南芥高尔基体的分离和蛋白质组学特性分析鉴定了参与植物细胞壁生物合成的功能和新的组成成分。
Plant Physiol. 2012 May;159(1):12-26. doi: 10.1104/pp.111.193151. Epub 2012 Mar 19.
5
Loss of Cellulose synthase-like F6 function affects mixed-linkage glucan deposition, cell wall mechanical properties, and defense responses in vegetative tissues of rice.纤维素合酶类似物 F6 功能丧失影响水稻营养组织中混合键合葡聚糖的沉积、细胞壁力学特性和防御反应。
Plant Physiol. 2012 May;159(1):56-69. doi: 10.1104/pp.112.195495. Epub 2012 Mar 2.
6
ARAD proteins associated with pectic Arabinan biosynthesis form complexes when transiently overexpressed in planta.ARAD 蛋白与果胶阿拉伯聚糖生物合成有关,在植物体内瞬时过表达时会形成复合物。
Planta. 2012 Jul;236(1):115-28. doi: 10.1007/s00425-012-1592-3. Epub 2012 Jan 21.
7
Tensional stress generation in gelatinous fibres: a review and possible mechanism based on cell-wall structure and composition.凝胶态纤维中张应力的产生:基于细胞壁结构和组成的综述及可能的机制。
J Exp Bot. 2012 Jan;63(2):551-65. doi: 10.1093/jxb/err339. Epub 2011 Nov 16.
8
GABI-Kat SimpleSearch: new features of the Arabidopsis thaliana T-DNA mutant database.GABI-Kat SimpleSearch:拟南芥 T-DNA 突变体数据库的新功能。
Nucleic Acids Res. 2012 Jan;40(Database issue):D1211-5. doi: 10.1093/nar/gkr1047. Epub 2011 Nov 12.
9
Development of cellulosic secondary walls in flax fibers requires beta-galactosidase.亚麻纤维中纤维素次生壁的形成需要β-半乳糖苷酶。
Plant Physiol. 2011 Jul;156(3):1351-63. doi: 10.1104/pp.111.172676. Epub 2011 May 19.
10
MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods.MEGA5:用于最大似然法、进化距离法和最大简约法的分子进化遗传学分析。
Mol Biol Evol. 2011 Oct;28(10):2731-9. doi: 10.1093/molbev/msr121. Epub 2011 May 4.