3-Hydroxypropanal (BioDeep_00001868711)

Main id: BioDeep_00000004528

 

PANOMIX_OTCML-2023


代谢物信息卡片


3-Hydroxypropanal

化学式: C3H6O2 (74.0368)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C(C=O)CO
InChI: InChI=1S/C3H6O2/c4-2-1-3-5/h2,5H,1,3H2

描述信息

Reuterin is a broad-spectrum antimicrobial agent active against Gram positive and Gram negative bacteria, as well as yeasts, moulds and protozoa. Reuterin is produced by specific strains of Lactobacillus reuteri during anaerobic metabolism of glycerol. Reuterin also demonstrates potent antimicrobial activity against a broad panel of human and poultry meat campylobacter spp. Isolates[1][2].

同义名列表

4 个代谢物同义名

3-Hydroxypropanal; 3-Hydroxypropionaldehyde; Reuterin; 3-Hydroxypropanal



数据库引用编号

11 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(3)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

0 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 5 DERA, GAPDH, GK, GPD1, LPO
Peripheral membrane protein 2 CYP1B1, HSD17B6
Endoplasmic reticulum membrane 1 CYP1B1
Nucleus 6 DERA, EBF1, EMX2, GAPDH, GK, SP4
cytosol 9 ADH6, ADH7, AKR1A1, DERA, GAPDH, GK, GPD1, NAPRT, SP4
nucleoplasm 3 DERA, GLDC, SP4
Cell membrane 1 TNF
Cell projection, axon 1 EMX2
Cytoplasmic granule 1 DERA
Early endosome membrane 1 HSD17B6
Synapse 1 AKR1A1
cell surface 1 TNF
neuronal cell body 1 TNF
Cytoplasm, cytosol 4 AKR1A1, GAPDH, GK, NAPRT
plasma membrane 4 ADH7, GAPDH, GLDC, TNF
Membrane 2 CYP1B1, GAPDH
apical plasma membrane 1 AKR1A1
axon 1 EMX2
basolateral plasma membrane 1 LPO
extracellular exosome 8 ADH6, AKR1A1, BMP3, GAPDH, GK, GPD1, LPO, NAPRT
Lumenal side 1 HSD17B6
endoplasmic reticulum 1 HSD17B6
extracellular space 7 AKR1A1, BMP3, CXCL8, DEFB4B, IL10, LPO, TNF
perinuclear region of cytoplasm 1 GAPDH
mitochondrion 3 CYP1B1, GK, GLDC
intracellular membrane-bounded organelle 3 CYP1B1, GAPDH, HSD17B6
Microsome membrane 2 CYP1B1, HSD17B6
Secreted 5 BMP3, CXCL8, DEFB4B, IL10, LPO
extracellular region 8 BMP3, CXCL8, DEFB4B, DERA, IL10, LPO, NAPRT, TNF
Mitochondrion outer membrane 1 GK
Single-pass membrane protein 1 GK
mitochondrial outer membrane 1 GK
mitochondrial matrix 1 GLDC
nuclear membrane 1 GAPDH
external side of plasma membrane 1 TNF
microtubule cytoskeleton 1 GAPDH
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
vesicle 1 GAPDH
Apical cell membrane 1 AKR1A1
Cytoplasm, perinuclear region 1 GAPDH
Membrane raft 1 TNF
Cytoplasm, cytoskeleton 1 GAPDH
chromatin 3 EBF1, EMX2, SP4
phagocytic cup 1 TNF
cytoskeleton 1 GAPDH
Lipid droplet 1 GAPDH
[Isoform 4]: Cytoplasm, cytosol 1 GK
ficolin-1-rich granule lumen 1 DERA
secretory granule lumen 1 DERA
Golgi lumen 1 DEFB4B
azurophil granule lumen 1 NAPRT
ribonucleoprotein complex 1 GAPDH
GAIT complex 1 GAPDH
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
glycine cleavage complex 1 GLDC
[Isoform 3]: Mitochondrion outer membrane 1 GK
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Nupur K Das, Andrew J Schwartz, Gabrielle Barthel, Naohiro Inohara, Qing Liu, Amanda Sankar, David R Hill, Xiaoya Ma, Olivia Lamberg, Matthew K Schnizlein, Juan L Arqués, Jason R Spence, Gabriel Nunez, Andrew D Patterson, Duxin Sun, Vincent B Young, Yatrik M Shah. Microbial Metabolite Signaling Is Required for Systemic Iron Homeostasis. Cell metabolism. 2020 01; 31(1):115-130.e6. doi: 10.1016/j.cmet.2019.10.005. [PMID: 31708445]
  • Falco Beer, Felix Urbat, Charles M A P Franz, Melanie Huch, Sabine E Kulling, Mirko Bunzel, Diana Bunzel. The Human Fecal Microbiota Metabolizes Foodborne Heterocyclic Aromatic Amines by Reuterin Conjugation and Further Transformations. Molecular nutrition & food research. 2019 05; 63(10):e1801177. doi: 10.1002/mnfr.201801177. [PMID: 30815965]
  • Jennifer K Spinler, Jennifer Auchtung, Aaron Brown, Prapaporn Boonma, Numan Oezguen, Caná L Ross, Ruth Ann Luna, Jessica Runge, James Versalovic, Alex Peniche, Sara M Dann, Robert A Britton, Anthony Haag, Tor C Savidge. Next-Generation Probiotics Targeting Clostridium difficile through Precursor-Directed Antimicrobial Biosynthesis. Infection and immunity. 2017 10; 85(10):. doi: 10.1128/iai.00303-17. [PMID: 28760934]
  • Juntana Chimchang, Talent Theparee, Boonyarut Ladda, Somboon Tanasupawat, Benjamas Thanomsub Wongsatayanon, Malai Taweechotipatr. Antimicrobial Properties of a Potential Probiotic Lactobacillus from Thai Newborn Feces. Journal of the Medical Association of Thailand = Chotmaihet thangphaet. 2015 Oct; 98 Suppl 9(?):S116-22. doi: . [PMID: 26817219]
  • Laura R Jarboe. YqhD: a broad-substrate range aldehyde reductase with various applications in production of biorenewable fuels and chemicals. Applied microbiology and biotechnology. 2011 Jan; 89(2):249-57. doi: 10.1007/s00253-010-2912-9. [PMID: 20924577]
  • Le-Le Hu, Chen Chen, Tao Huang, Yu-Dong Cai, Kuo-Chen Chou. Predicting biological functions of compounds based on chemical-chemical interactions. PloS one. 2011; 6(12):e29491. doi: 10.1371/journal.pone.0029491. [PMID: 22220213]
  • Rosemarie De Weirdt, Sam Possemiers, Griet Vermeulen, Tanja C W Moerdijk-Poortvliet, Henricus T S Boschker, Willy Verstraete, Tom Van de Wiele. Human faecal microbiota display variable patterns of glycerol metabolism. FEMS microbiology ecology. 2010 Dec; 74(3):601-11. doi: 10.1111/j.1574-6941.2010.00974.x. [PMID: 20946352]
  • Rolene Bauer, Maret du Toit, Jens Kossmann. Influence of environmental parameters on production of the acrolein precursor 3-hydroxypropionaldehyde by Lactobacillus reuteri DSMZ 20016 and its accumulation by wine lactobacilli. International journal of food microbiology. 2010 Jan; 137(1):28-31. doi: 10.1016/j.ijfoodmicro.2009.10.012. [PMID: 19897270]
  • Ronit Reich-Slotky, Christina A Kabbash, Phyllis Della-Latta, John S Blanchard, Steven J Feinmark, Sherry Freeman, Gilla Kaplan, Howard A Shuman, Samuel C Silverstein. Gemfibrozil inhibits Legionella pneumophila and Mycobacterium tuberculosis enoyl coenzyme A reductases and blocks intracellular growth of these bacteria in macrophages. Journal of bacteriology. 2009 Aug; 191(16):5262-71. doi: 10.1128/jb.00175-09. [PMID: 19429621]
  • Hidetoshi Morita, Hidehiro Toh, Shinji Fukuda, Hiroshi Horikawa, Kenshiro Oshima, Takehito Suzuki, Masaru Murakami, Shin Hisamatsu, Yukio Kato, Tatsuya Takizawa, Hideo Fukuoka, Tetsuhiko Yoshimura, Kikuji Itoh, Daniel J O'Sullivan, Larry L McKay, Hiroshi Ohno, Jun Kikuchi, Toshio Masaoka, Masahira Hattori. Comparative genome analysis of Lactobacillus reuteri and Lactobacillus fermentum reveal a genomic island for reuterin and cobalamin production. DNA research : an international journal for rapid publication of reports on genes and genomes. 2008 Jun; 15(3):151-61. doi: 10.1093/dnares/dsn009. [PMID: 18487258]
  • Valentine Cleusix, Christophe Lacroix, Sabine Vollenweider, Gwenaëlle Le Blay. Glycerol induces reuterin production and decreases Escherichia coli population in an in vitro model of colonic fermentation with immobilized human feces. FEMS microbiology ecology. 2008 Jan; 63(1):56-64. doi: 10.1111/j.1574-6941.2007.00412.x. [PMID: 18028400]
  • S McCoy, S E Gilliland. Isolation and characterization of Lactobacillus species having potential for use as probiotic cultures for dogs. Journal of food science. 2007 Apr; 72(3):M94-7. doi: 10.1111/j.1750-3841.2007.00310.x. [PMID: 17995807]
  • E Rodríguez, J L Arqués, R Rodríguez, M Nuñez, M Medina. Reuterin production by lactobacilli isolated from pig faeces and evaluation of probiotic traits. Letters in applied microbiology. 2003; 37(3):259-63. doi: 10.1046/j.1472-765x.2003.01390.x. [PMID: 12904230]