Entry
Name
(3S,6E)-nerolidol synthase;
(E)-nerolidol synthase;
nerolidol synthase;
(3S)-(E)-nerolidol synthase;
FaNES1
Class
Lyases;
Carbon-oxygen lyases;
Acting on phosphates
BRITE hierarchy
Sysname
(2E,6E)-farnesyl-diphosphate diphosphate-lyase [(3S,6E)-nerolidol-forming]
Reaction(IUBMB)
(2E,6E)-farnesyl diphosphate + H2O = (3S,6E)-nerolidol + diphosphate [RN:
R08374 ]
Reaction(KEGG)
Substrate
Product
Comment
The enzyme catalyses a step in the formation of (3E)-4,8-dimethylnona-1,3,7-triene, a key signal molecule in induced plant defense mediated by the attraction of enemies of herbivores [2]. Nerolidol is a naturally occurring sesquiterpene found in the essential oils of many types of plants.
History
EC 4.2.3.48 created 2010
Pathway
ec00909 Sesquiterpenoid and triterpenoid biosynthesis
Orthology
K14175 (3S,6E)-nerolidol synthase
Genes
CIT : 102617431 102617651 102617908 102620886
CIC : CICLE_v10004558mg CICLE_v10014632mg CICLE_v10014707mg
PVY : 116111381 116121150 116145960
MINC : 123192358 123192360 123192601 123192665 123192702
TCC : 108662607 18597023 18597024
EGR : 104445481 104447370 104447372 104447373 104447374 104447375 104447392 104447394 104447396 104447399
GMX : 100782471(TPS4) 100783015(TPS5) 100814957(TPS6)
PVU : PHAVU_002G219100g PHAVU_002G219300g
VRA : 106765590 106766355 106766356 106766374
VAR : 108326386 108338184 108338349
VUN : 114177509 114178712 114178713 114179677
CCAJ : 109814060 109817871 109817878
MTR : MTR_4g092010 MTR_4g092020
CAM : 101494917 101495572 101503644
LJA : Lj0g3v0198989.1(Lj0g3v0198989.1) Lj0g3v0198989.2(Lj0g3v0198989.2)
AHF : 112714726 112728647 112784898 112791359
RCN : 112165597 112166460 112202907
PMUM : 103324596 103343969
PAVI : 110752892 110768753
PDUL : 117625092 117626312
MDM : 103434640 103446596 103446597 103446598(LIS) 114827793
PXB : 103941370 103941371 103958297
MNT : 21385024 21408693 21408694
CMO : 103485748 103485753 103485759 103489227
BHJ : 120080989 120082587 120082664 120082764 120083563
MCHA : 111010706 111010875 111010876 111010887
CMAX : 111484385 111490118
CMOS : 111434067 111434068 111447175 111456834
CPEP : 111783518 111802148
JCU : 105629808 105629819 105629820 105649410
HBR : 110635396 110644414 110654947 110661963
MESC : 110603115 110604308 110604309 110605593
POP : 18102943 7490762 7490764
PALZ : 118031658 118031660 118031663 118042815
JRE : 108979322 108979323 108989344 109004686 109004723 109007398 109013445
QSU : 111988830 111989102 111989152
QLO : 115988645 115991201 115992647 115992733
VVI : 100248531 100266449(LinNer) 100267150 100852561 100852596 100852776 100853562 100853639 100853679 100854717 100854809
VRI : 117910457 117910459 117910461 117910462 117918890 117923388 117924000 117924001 117924133
SLY : 101244812(TPS37) 101245403(TPS39)
SPEN : 107019618 107032586
INI : 109163834 109167275 109167276 109167277 109167278 109167279
ITR : 116029121 116029228 116029229 116029230 116029231 116029232 116029233 116030387 116030506 116030578
SIND : 105156792 105175396 105175430 105175469 105175470
OEU : 111395219 111396005 111396006 111396009 111396013 111396015 111396016
SSPL : 121759727 121783505 121787949 121794424
HAN : 110884314 110889629 110915780 110916766 110919641
ECAD : 122597840 122599361 122608148
LSV : 111884934 111897116 111897141 111897149
CCAV : 112527638 112527948
DCR : 108194757 108195481 108195714 108195795 108195952
CSIN : 114261430 114266222 114282497 114288835 114290333
BVG : 104883052 104901069 104901071
CQI : 110687149 110687263 110693359 110693461 110693462
MING : 122059466 122059660 122061859 122072008 122072223 122092317 122092318
TSS : 122638603 122639517 122667458 122667459 122668202
NCOL : 116246448 116246454 116247351
ATR : 18431529 18440985 18440990
» show all
Taxonomy
Reference
Authors
Aharoni A, Giri AP, Verstappen FW, Bertea CM, Sevenier R, Sun Z, Jongsma MA, Schwab W, Bouwmeester HJ
Title
Gain and loss of fruit flavor compounds produced by wild and cultivated strawberry species.
Journal
Reference
Authors
Bouwmeester HJ, Verstappen FW, Posthumus MA, Dicke M
Title
Spider mite-induced (3S)-(E)-nerolidol synthase activity in cucumber and lima bean. The first dedicated step in acyclic C11-homoterpene biosynthesis.
Journal
Reference
Authors
Degenhardt J, Gershenzon J
Title
Demonstration and characterization of (E)-nerolidol synthase from maize: a herbivore-inducible terpene synthase participating in (3E)-4,8-dimethyl-1,3,7-nonatriene biosynthesis.
Journal
Reference
Authors
Arimura G, Garms S, Maffei M, Bossi S, Schulze B, Leitner M, Mithofer A, Boland W
Title
Herbivore-induced terpenoid emission in Medicago truncatula: concerted action of jasmonate, ethylene and calcium signaling.
Journal
Sequence
Other DBs
ExplorEnz - The Enzyme Database: 4.2.3.48
ExPASy - ENZYME nomenclature database: 4.2.3.48
LinkDB
All DBs