KEGG PATHWAY: ec00907

PATHWAY: ec00907

Entry

ec00907                     Pathway

Name

Pinene, camphor and geraniol degradation

Class

Metabolism; Metabolism of terpenoids and polyketides

Pathway map

ec00907

Pinene, camphor and geraniol degradation

Other DBs

GO:	0033074 0019383 1903447

Enzyme

1.1.1.183

1.1.1.327

1.1.1.347

1.1.1.35

1.14.13.160

1.14.13.161

1.14.14.108

1.14.14.155

1.14.15.1

1.14.15.10

1.2.1.86

2.3.1.16

3.7.1.18

4.1.3.26

4.1.3.4

4.2.1.17

4.2.1.57

5.5.1.10

6.2.1.38

6.4.1.5

Compound

C00024

Acetyl-CoA

C00630

2-Methylpropanoyl-CoA

C00808

(+)-Camphor

C00809

(-)-Camphor

C01291

3-(4-Methylpent-3-en-1-yl)pent-2-enedioyl-CoA

C01499

Geranial

C01500

Geraniol

C01920

Geranoyl-CoA

C02759

alpha-Pinene-oxide

C02952

5-Oxo-1,2-campholide

C03037

(+)-Bornane-2,5-dione

C03069

3-Methylcrotonyl-CoA

C03448

(+)-exo-5-Hydroxycamphor

C04435

(Z)-2-Methyl-5-isopropylhexa-2,5-dienal

C04675

3-Hydroxy-3-(4-methylpent-3-en-1-yl)glutaryl-CoA

C07160

[(1R)-2,2,3-Trimethyl-5-oxocyclopent-3-enyl]acetyl-CoA

C09847

cis-Citral

C09848

(R)-(+)-Citronellal

C09849

beta-Citronellol

C09871

Nerol

C09880

alpha-Pinene

C09884

Pinocarvone

C11384

(S)-(-)-Citronellal

C11386

(-)-Citronellol

C11938

Myrtenol

C11939

Myrtenal

C11940

Myrtenic acid

C11941

Pinocarveol

C11942

trans-2-Methyl-5-isopropylhexa-2,5-dienal

C11943

trans-2-Methyl-5-isopropylhexa-2,5-dienoic acid

C11944

cis-2-Methyl-5-isopropylhexa-2,5-dienoic acid

C11945

trans-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA

C11946

cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA

C11947

3-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-CoA

C11948

2,6-Dimethyl-5-methylene-3-oxo-heptanoyl-CoA

C11949

3-Isopropylbut-3-enoyl-CoA

C11950

3-Isopropyl-3-butenoic acid

C16461

Geranic acid

C16462

Citronellate

C16464

Citronellyl-CoA

C16465

trans-Geranyl-CoA

C16466

7-Methyl-3-oxo-6-octenoyl-CoA

C16468

(2E)-5-Methylhexa-2,4-dienoyl-CoA

C16469

3-Hydroxy-5-methylhex-4-enoyl-CoA

C16470

5-Methylhex-4-enoyl-CoA

C16471

5-Methyl-3-oxo-4-hexenoyl-CoA

C20271

[(1R)-2,2,3-Trimethyl-5-oxocyclopent-3-enyl]acetate

C20320

Bornane-2,6-dione

C20321

[(2R)-3,3,4-Trimethyl-6-oxo-3,6-dihydro-1H-pyran-2-yl]acetyl-CoA

C20322

(+)-6-exo-Hydroxycamphor

C20323

(+)-6-endo-Hydroxycamphor

C20324

[(1S)-4-Hydroxy-2,2,3-trimethylcyclopent-3-enyl]acetate

C21929

(-)-Bornane-2,5-dione

C21930

(-)-5-Oxo-1,2-campholide

C22610

(-)-3-exo-Hydroxycamphor

Reference

PMID:11778886

Authors

Wolken WA, van der Werf MJ.

Title

Geraniol biotransformation-pathway in spores of Penicillium digitatum.

Journal

Appl Microbiol Biotechnol 57:731-7 (2001)
DOI:10.1007/s002530100821

Reference

PMID:16272386

Authors

Hoschle B, Gnau V, Jendrossek D.

Title

Methylcrotonyl-CoA and geranyl-CoA carboxylases are involved in leucine/isovalerate utilization (Liu) and acyclic terpene utilization (Atu), and are encoded by liuB/liuD and atuC/atuF, in Pseudomonas aeruginosa.

Journal

Microbiology 151:3649-56 (2005)
DOI:10.1099/mic.0.28260-0

Reference

PMID:16820476

Authors

Forster-Fromme K, Hoschle B, Mack C, Bott M, Armbruster W, Jendrossek D

Title

Identification of genes and proteins necessary for catabolism of acyclic terpenes and leucine/isovalerate in Pseudomonas aeruginosa.

Journal

Appl Environ Microbiol 72:4819-28 (2006)
DOI:10.1128/AEM.00853-06

Reference

PMID:16000717

Authors

Hoschle B, Jendrossek D.

Title

Utilization of geraniol is dependent on molybdenum in Pseudomonas aeruginosa: evidence for different metabolic routes for oxidation of geraniol and citronellol.

Journal

Microbiology 151:2277-83 (2005)
DOI:10.1099/mic.0.27957-0

Reference

PMID:681275

Authors

Cantwell SG, Lau EP, Watt DS, Fall RR.

Title

Biodegradation of acyclic isoprenoids by Pseudomonas species.

Journal

J Bacteriol 135:324-33 (1978)
DOI:10.1128/JB.135.2.324-333.1978

Reference

PMID:19597963