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. 2020 Dec 14;10:21861. doi: 10.1038/s41598-020-78873-3

Table 1.

Summary of highly correlated metabolites in different biosynthetic pathways.

Biosynthetic pathways p-value Metabolites
Phenylpropanoid derivatives biosynthesisa 2.56e−05 Quercetina,b,c,d,e,f,g,j,q
Superpathway of flavones and derivatives biosynthesisb 4.65e−04 Luteolina,d,g,j,n
Flavonols biosynthesisc 7.48e−04 Syringina,j,k
Flavonoids biosynthesisd 1.18e−03 Kaempferol-3-glucosidea,b,c,d,j
Rutin biosynthesise 2.95e−03 Rutina,b,c,d,e,j
Quercetin glycoside biosynthesis (Arabidopsis)f 5.07E−03 Benzoatea,j,m,p
Flavonoid biosynthesis (In Equisetum)g 7.72e−03 Coniferina,j,k,p,r
Proteinogenic amino acids biosynthesish 2.26e−03 Quercetin 3-O-rhamnosidea,b,c,d,f,j
Amino acids biosynthesish 6.54e−03 l-Arginineh,i,p,s
Proteinogenic amino acids degradationi 8.72e−03 l-Tryptophanh,i,j,p
Amino acids degradationi 1.07e−02 Adenineh,l,p,t
Secondary metabolites biosynthesisj 1.29e−02 l-Isoleucineh,i
Lignins biosynthesisk 2.31e−02 Adenosineh,i,o,p,t
S-methyl-5′-thioadenosine degradation iil 2.59E−02 l-Isoleucinep
Benzoyl-β-d-glucopyranose biosynthesism 2.59E−02
Benzoate degradationm 3.86e−02
Benzoate degradation II (aerobic and anaerobic)m 3.86E−02
Chrysoeriol biosynthesisn 3.23e−02
Adenine and adenosine salvage VIo 3.23E−02
Degradation/utilization/assimilationp 3.35e−02
Methylquercetin biosynthesisq 3.86e−02
Phenylpropanoid derivatives degradationr 4.49e−02
Coniferin metabolismr 4.49e−02
Putrescine biosynthesis Is 4.49E−02
Adenine and adenosine salvage IIt 8.13E−04
Adenine and adenosine salvaget 1.72E−03
Purine Nucleosides Salvage II (Plant)t 2.95E−03
Cytokinins degradationt 3.43e−03
Purine nucleotide salvaget 7.72e−03
l-methionine salvaget 2.19E−02
l-methionine biosynthesist 3.06E−02
Purine nucleotide biosynthesist 4.04e−02

Letter(s) after the pathways and metabolites indicate the involved metabolites in the same pathway. Enrichment analysis was carried out using the Fisher Exact statistical test.