• 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

无光光生物化学

Photobiochemistry without light.

作者信息

Cilento G

机构信息

Department of Biochemistry, Universidade de São Paulo, Brazil.

出版信息

Experientia. 1988 Jul 15;44(7):572-6. doi: 10.1007/BF01953304.

DOI:10.1007/BF01953304
PMID:3294032
Abstract

Efficient excited state formation - much higher than that hitherto expected - may occur in organelles and in intact cells. Excited triplet states can be enzymatically generated in high yields by different routes. An example is the oxidation of isobutanal to acetone and formic acid, catalyzed by horseradish peroxidase. Other enzymatic systems that generate triplet carbonyls are linear aliphatic aldehydes when oxidized by peroxidase/O2, or the indole-3-acetic acid/peroxidase/O2-reaction. The latter is widespread in plants. This new field - photobiochemistry without light - has led to a growing awareness of the idea that cells may utilize excited states to trigger photochemical processes even in the dark. Such phenomena are of considerable importance, also for the understanding of weak photon emission from biological systems.

摘要

在细胞器和完整细胞中可能会发生高效的激发态形成,其效率比迄今预期的要高得多。激发三重态可以通过不同途径以高产率酶促生成。一个例子是辣根过氧化物酶催化异丁醛氧化为丙酮和甲酸。其他产生三重态羰基的酶促系统包括过氧化物酶/氧气氧化线性脂肪醛,或吲哚 - 3 - 乙酸/过氧化物酶/氧气反应。后者在植物中广泛存在。这个新领域——无光光生物化学——已使人们越来越意识到,细胞甚至在黑暗中也可能利用激发态来触发光化学过程。此类现象对于理解生物系统的微弱光子发射也具有相当重要的意义。

相似文献

1
Photobiochemistry without light.无光光生物化学
Experientia. 1988 Jul 15;44(7):572-6. doi: 10.1007/BF01953304.
2
Excited singlet molecular O₂(¹Δg) is generated enzymatically from excited carbonyls in the dark.在黑暗中,激发态单线态分子氧(¹Δg)由激发态羰基通过酶促反应生成。
Sci Rep. 2014 Aug 4;4:5938. doi: 10.1038/srep05938.
3
Quenching of enzyme-generated acetone phosphorescence by indole compounds: stereospecific effects of D- and L-tryptophan. Photochemical-like effects.
Biochemistry. 1981 Dec 22;20(26):7329-33. doi: 10.1021/bi00529a001.
4
Singlet oxygen production from the peroxidase-catalyzed oxidation of indole-3-acetic acid.过氧化物酶催化吲哚 - 3 - 乙酸氧化产生单线态氧。
J Biol Chem. 1988 Oct 5;263(28):14171-5.
5
Enols of aldehydes in the peroxidase/oxidase-promoted generation of excited triplet species.
Biochim Biophys Acta. 1986 May 2;881(3):330-6. doi: 10.1016/0304-4165(86)90023-1.
6
Enzyme-generated electronically excited carbonyl compounds, Acetone phosphorescence during the peroxidase-catalyzed aerobic oxidation of isobutanal.
J Biol Chem. 1978 Jul 10;253(13):4707-12.
7
Hemin-catalyzed generation of triplet acetone.
Biochim Biophys Acta. 1980 Aug 1;631(1):203-9. doi: 10.1016/0304-4165(80)90068-9.
8
Excited indole-3-aldehyde from the peroxidase-catalyzed aerobic oxidation of indole-3-acetic acid. Reaction with and energy transfer to transfer ribonucleic acid.吲哚 - 3 - 乙酸经过氧化物酶催化的需氧氧化生成的激发态吲哚 - 3 - 醛。与转移核糖核酸的反应及能量转移。
Biochemistry. 1980 Nov 11;19(23):5270-5. doi: 10.1021/bi00564a019.
9
How Tryptophan Oxidation Arises by "Dark" Photoreactions from Chemiexcited Triplet Acetone.色氨酸氧化如何通过化学激发三重态丙酮的“暗”光反应产生。
Photochem Photobiol. 2021 Mar;97(2):456-459. doi: 10.1111/php.13375. Epub 2021 Jan 21.
10
1,3-diene probes for detection of triplet carbonyls in biological systems.用于检测生物系统中三重态羰基的1,3 - 二烯探针。
Chem Res Toxicol. 2007 Aug;20(8):1162-9. doi: 10.1021/tx700074n. Epub 2007 Jul 13.

引用本文的文献

1
Unexpected Reaction Pathway of the Alpha-Aminoalkyl Radical Derived from One-Electron Oxidation of -Alkylglutathiones.- 烷基谷胱甘肽的单电子氧化生成的α-氨基酸烷基自由基的意外反应途径。
Molecules. 2020 Feb 17;25(4):877. doi: 10.3390/molecules25040877.
2
Detection of Ultraweak Photon Emission (UPE) from Cells as a Tool for Pathological Studies.检测细胞的超微弱光子发射(UPE)作为病理研究的一种工具。
J Biomed Phys Eng. 2017 Dec 1;7(4):389-396. eCollection 2017 Dec.
3
Enhancement of biophoton emission of prostate cancer cells by Ag nanoparticles.

本文引用的文献

1
The oxidation of phenyl-acetaldehyde by plant saps.植物汁液对苯乙醛的氧化作用。
Biochem J. 1953 Sep;55(2):350-60. doi: 10.1042/bj0550350.
2
Much of spontaneous mutagenesis in Escherichia coli is due to error-prone DNA repair: implications for spontaneous carcinogenesis.大肠杆菌中许多自发突变是由于易错DNA修复:对自发致癌作用的影响。
Carcinogenesis. 1981;2(9):863-72. doi: 10.1093/carcin/2.9.863.
3
Biological chemiluminescence.生物化学发光
银纳米颗粒增强前列腺癌细胞的生物光子发射
Cancer Nanotechnol. 2013;4(1-3):21-26. doi: 10.1007/s12645-013-0034-7. Epub 2013 Mar 28.
4
Imaging of ultra-weak photon emission in a rheumatoid arthritis mouse model.类风湿性关节炎小鼠模型中超弱光子发射的成像
PLoS One. 2013 Dec 30;8(12):e84579. doi: 10.1371/journal.pone.0084579. eCollection 2013.
5
Secondary Ultraweak Luminescence from Humic Acids Induced by gamma-Radiation.γ辐射诱导腐殖酸产生的次级超微弱发光
Nonlinearity Biol Toxicol Med. 2004 Jul;2(3):245-58. doi: 10.1080/15401420490507468.
6
Nonlinear response of biophoton emission to external perturbations.生物光子发射对外界扰动的非线性响应。
Experientia. 1992 Dec 1;48(11-12):1069-82. doi: 10.1007/BF01947994.
Photochem Photobiol. 1984 Dec;40(6):823-30. doi: 10.1111/j.1751-1097.1984.tb04657.x.
4
Peroxidase-catalyzed formation of triplet acetone and chemiluminescence from isobutyraldehyde and molecular oxygen.过氧化物酶催化生成三重态丙酮以及异丁醛与分子氧发生化学发光反应。
J Biol Chem. 1985 Aug 25;260(18):10217-25.
5
Metabolically-produced 'UV-like' DNA damage and its role in spontaneous mutagenesis.
Photochem Photobiol. 1985 Dec;42(6):801-3. doi: 10.1111/j.1751-1097.1985.tb01652.x.
6
Intracellular generation of electronically excited states. Polymorphonuclear leukocytes challenged with a precursor of triplet acetone.
Biochim Biophys Acta. 1986 May 2;881(3):337-42. doi: 10.1016/0304-4165(86)90024-3.
7
Enols of aldehydes in the peroxidase/oxidase-promoted generation of excited triplet species.
Biochim Biophys Acta. 1986 May 2;881(3):330-6. doi: 10.1016/0304-4165(86)90023-1.
8
Activation of urocanase from Pseudomonas putida by electronically excited triplet species.
J Biol Chem. 1985 Oct 5;260(22):12190-3.