KEGG   ENZYME: 4.3.3.9
Entry
EC 4.3.3.9                  Enzyme                                 
Name
indigoidine synthase;
bspA (gene name)
Class
Lyases;
Carbon-nitrogen lyases;
Amine-lyases
Sysname
L-glutamine oxidoreductase/cyclase (3-amino-1,5-dihydropyridine-2,6-dione-forming)
Reaction(IUBMB)
2 ATP + 2 L-glutamine + O2 + 2 FMN = 2 AMP + 2 diphosphate + indigoidine + 2 H2O + 2 FMNH2 (overall reaction) [RN:R13355];
(1a) 2 ATP + 2 L-glutamine + 2 FMN = 2 AMP + 2 diphosphate + 2 3-amino-1,5-dihydropyridine-2,6-dione + FMNH2 [RN:R13353];
(1b) 2 3-amino-1,5-dihydropyridine-2,6-dione + O2 = indigoidine + 2 H2O (spontaneous) [RN:R13354]
Reaction(KEGG)
Substrate
ATP [CPD:C00002];
L-glutamine [CPD:C00064];
O2 [CPD:C00007];
FMN [CPD:C00061];
3-amino-1,5-dihydropyridine-2,6-dione [CPD:C22943]
Product
AMP [CPD:C00020];
diphosphate [CPD:C00013];
indigoidine [CPD:C22944];
H2O [CPD:C00001];
FMNH2 [CPD:C01847];
3-amino-1,5-dihydropyridine-2,6-dione [CPD:C22943]
Comment
The enzyme, found in a number of bacterial strains, is a non-ribosomal peptide synthase (NRPS). The enzyme forms 3-amino-1,5-dihydropyridine-2,6-dione, which undergoes spontaneous oxidation to form the blue pigment indigoidine.
History
EC 4.3.3.9 created 2024
Orthology
K27871  indigoidine synthase
Genes
SPESpro_1698
SQUE4343_07645
DDDDda3937_00972(indC)
DZEDd1591_0073
DDCDd586_0084
DZCW909_00340
DSOA4U42_09535
CEDLH89_11810
DFNCVE23_00465
DDQDDI_4393
DAQDAQ1742_04343(indC)
DICDpoa569_0003841
ETPLU633_16190
PLUplu2186
PLUMA4R40_10965
PAYPAU_02362
PTTVY86_20065
XPOXPG1_0720
VNIVIBNI_B0265(bpsA)
VSRVspart_04306(tycC_7)
VRURND59_00295
ACVAMD27_12430
PBWD172_001470
PRRAT705_17200
PNGPNIG_a0231(ofaC)
PAEWKIH87_06045
MMAAFR932_08020
BGDbgla_2g17770
PBHAAW51_5194
RJGCCGE525_37390
RTUPR017_21845
ARAArad_12458
LEJETW24_21400
LAQUR2C4_02970
LCAEK3721_19825
AVMJQX13_29175
PIJQEJ31_09450
CARCAQ58242.1
CGVCGLAU_10015(tycC)
CSTRCBE89_13190
WHROG579_02790
SALBXNR_5634
SFISFUL_2479 SFUL_5936
SCYER2B67_31530
SVESVEN_4086
SDVBN159_7970(indC)
SVTSVTN_21155
STREGZL_01654
SCZABE83_23580
SRNA4G23_04733(ppsD)
SNRSNOUR_41230
SPLULK06_027050
SLAUSLA_4174
SLXSLAV_40115(tycC5)
SGDELQ87_09885
SSPODDQ41_19505
SCAVCVT27_10965
SGXH4W23_22610
SBROGQF42_31590
SHARHUT13_01155
SFBCP974_25355
SROIIAG44_11750
SMAOCAG99_14340
SGOBtest1122_13725
STAALDH80_18160
SYUNMOV08_06930
SHAUK9S39_05015
SCOAQU709_03980
SCAYPYS65_05785
KBUQ4V64_07135
KABB7C62_03605
CMHVO01_05770
CUYI8920_00995
RSARSal33209_1837
SATKSA2016_3652
BLUTEW640_11710
AERAERYTH_13670
NOABKM31_11375
MHAIOHB01_07065
AOIAORI_6000
AJAAJAP_09435
AMYBBKN51_23530
AORISD37_29415
ACYNORV05_18235
AMYEMJQ72_29340
LEDBBK82_06850
UMERM788_06215
MICHFJK98_13995
PSUUPsuf_005290
DROSDrose_28380
NAVJQS30_13885
NOSUJYQ62_14450
 » show all
Reference
1  [PMID:11790734]
  Authors
Reverchon S, Rouanet C, Expert D, Nasser W.
  Title
Characterization of indigoidine biosynthetic genes in Erwinia chrysanthemi and role of this blue pigment in pathogenicity.
  Journal
J Bacteriol 184:654-65 (2002)
DOI:10.1128/JB.184.3.654-665.2002
  Sequence
Reference
2  [PMID:17237222]
  Authors
Takahashi H, Kumagai T, Kitani K, Mori M, Matoba Y, Sugiyama M.
  Title
Cloning and characterization of a Streptomyces single module type non-ribosomal peptide synthetase catalyzing a blue pigment synthesis.
  Journal
J Biol Chem 282:9073-81 (2007)
DOI:10.1074/jbc.M611319200
  Sequence
Reference
3  [PMID:23051833]
  Authors
Walsh CT, Wencewicz TA.
  Title
Flavoenzymes: versatile catalysts in biosynthetic pathways.
  Journal
Nat Prod Rep 30:175-200 (2013)
DOI:10.1039/c2np20069d
Other DBs
ExplorEnz - The Enzyme Database: 4.3.3.9
IUBMB Enzyme Nomenclature: 4.3.3.9
ExPASy - ENZYME nomenclature database: 4.3.3.9
BRENDA, the Enzyme Database: 4.3.3.9
LinkDB

DBGET integrated database retrieval system