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Table 2 The secondary metabolites from the selected isolate SYP-A7257 analyzed by LC-MS

From: Insights into Streptomyces spp. isolated from the rhizospheric soil of Panax notoginseng: isolation, antimicrobial activity and biosynthetic potential for polyketides and non-ribosomal peptides

No.

Retention time (min)

Molecular formula

Ion molecular formula

m/z

m/z (Calc)

Deviation (ppm)

Compound

UV (CH3CN-H2O) (nm)

Structural class

Reference (s)

Activity

F5

25.688

C33H53O12

C33H54NaO12

665.3505

665.3507

0.37

1′, 14-Dihydroxyisochainin

325, 340, 360

polyene macrolides

[31]

antifungal

F6

28.963

C35H57O13

C35H58NaO13

709.3771

709.377

−0.19

hydrofungichromin

325, 340, 360

polyene macrolides

New compound

ND

F2

31.555

C35H57O12

C35H58NaO12

693.3818

693.382

0.36

fungichromin

325, 340, 360

polyene macrolides

[32]

antifungal

F3

40.872

C62H85N12O17

C62H86N12NaO17

1293.6149

1293.6126

−1.77

Actinomycin X0β

241, 446

PKS-NRPS hybrid

[33]

antibacteria

F1

42.672

C62H84N12O17

C62H85N12O17

1269.6146

1269.615

0.33

Actinomycin X2

241, 446

PKS-NRPS hybrid

[33]

antibacteria

F4

43.398

C62H85N12O16

C62H86N12NaO16

1277.6161

1277.6177

−4.39

Actinomycin D

241, 446

PKS-NRPS hybrid

[33]

antibacteria

  1. ND, not determined because of insufficient amounts of compounds