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. 2017 Jan 23;22(1):176. doi: 10.3390/molecules22010176

Table 2.

Microbial producers of AChEIs.

Strain Classification Structure of Active Ingredient(s) Compound Type IC50 Method Used Ref.
Aspergillus terreus Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Moniliaceae,
Aspergillus
graphic file with name molecules-22-00176-i001.jpg Territrem B 7.6 μM Ellman’s method Ling et al. [25]
Aspergillus terreus
(No. GX7-3B)
Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Moniliaceae,
Aspergillus
graphic file with name molecules-22-00176-i002.jpg Anhydrojavanicin 2.01 μM Modified Ellman’s method Deng et al. [26]
graphic file with name molecules-22-00176-i003.jpg 8-O-Methylbostrycoidin 6.71 μM
graphic file with name molecules-22-00176-i004.jpg NGA0187 (Terpenoid) 1.89 μM
graphic file with name molecules-22-00176-i005.jpg Beauvericin 3.09 μM
Aspergillus flavus LF40 Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Moniliaceae,
Aspergillus
graphic file with name molecules-22-00176-i006.jpg Huperzine A 0.6 μM Modified Ellman’s method Wang et al. [27]
Aspergillus flavus Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Moniliaceae,
Aspergillus
graphic file with name molecules-22-00176-i007.jpg (8E,12Z)-10,11-Dihydroxyoctadeca-8,12-dienoic acid No report Modified Ellman’s method Qiao et al. [28]
graphic file with name molecules-22-00176-i008.jpg 3β,4α-Dihydroxy-26-methoxyergosta-7,24(28)-dien-6-one
Aspergillus versicolor
Y10
Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Moniliaceae,
Aspergillus
graphic file with name molecules-22-00176-i009.jpg Avertoxin B 14.9 μM Modified Ellman’s method Wang et al. [29]
Penicillium citrinum Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Moniliaceae,
Penicillium
graphic file with name molecules-22-00176-i010.jpg Quinolactacins A1 280 μM Modified Ellman’s method Kim et al. [30]
graphic file with name molecules-22-00176-i011.jpg Quinolactacins A2 19.8 μM
Penicillium sp.
EPF-6
Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Moniliaceae,
Penicillium
graphic file with name molecules-22-00176-i012.jpg Quinolactacins A, B, and C No report Ellman’s method Kakinuma et al. [31]
Penicillium sp.
FO-4259
Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Moniliaceae,
Penicillium
graphic file with name molecules-22-00176-i013.jpg Arigsugacin I 0.64 μM Modified Ellman’s method Omura et al.; Huang et al. [32,33]
Penicillium sp.
sk5GW1L
Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Moniliaceae,
Penicillium
Arigsugacins F 0.37 μM
Territrem B 7.03 μM
Penicillium chermesinum
(ZH4-E2)
Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Moniliaceae,
Penicillium
graphic file with name molecules-22-00176-i014.jpg Terphenyls 7.8 μM
5.2 μM
Modified Ellman’s method Huang et al. [34]
Penicillium griseofulvum
LF146
Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Moniliaceae,
Penicillium
graphic file with name molecules-22-00176-i015.jpg Huperzine A 0.6 μM Modified Ellman’s method Wang et al. [35]
Paecilomyces tenuis
YS-13
Eumycota,
Deuteromycotina,
Hyphomycetes,
Paecilomyces Paecilomyces
graphic file with name molecules-22-00176-i016.jpg Huperzine A 0.6 μM Modified Ellman’s method Su and Yang [36]
Acremonium implicatum
LF30
Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Moniliaceae,
Acremonium
No clear products Modified Ellman’s method Wang et al. [35]
Acremonium sp.
2F09P03B
Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Moniliaceae,
Acremonium
graphic file with name molecules-22-00176-i017.jpg Huperzine A 0.6 μM No report Li et al. [37]
Botrytis sp.
HA23
Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Moniliaceae,
Botrytis
graphic file with name molecules-22-00176-i018.jpg Huperzine A 0.6 μM No report Ju et al. [38]
Trichoderma sp. Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Moniliaceae,
Trichoderma
No clear products Modified Ellman’s method Dong et al. [39]
Colletotrichum gloeosporioides
ES026
Eumycota,
Deuteromycotina,
Coelomycetes,
Melanconiales,
Melanconiaceae Colletotrichum
graphic file with name molecules-22-00176-i019.jpg Huperzine A 0.6 μM Modified Ellman’s method Zhao et al. [40]
Alternaria sp.
YD-01
Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Dematiaceae Alternaria
graphic file with name molecules-22-00176-i020.jpg Huperzine A 0.6 μM TLC bioautography Yang et al. [41]
Cladosporium cladosporioides
LF70
Eumycota,
Deuteromycotina,
Hyphomycetes,
Moniliales,
Dermateaceae,
Cladosporium
graphic file with name molecules-22-00176-i021.jpg Huperzine A 0.6 μM
Phomopsis sp. Eumycota,
Deuteromycotina,
Coelamycetes,
Sphaeropsidales,
Sphaeropsidaceae,
Phomopsis
graphic file with name molecules-22-00176-i022.jpg Cytochalasin H No report TLC bioautography Chapla et al. [42]
Chrysosporium sp. Eumycota,
Ascomycotina,
Ascomycetes,
Onygenales,
Onygenaceae, Chrysosporium
graphic file with name molecules-22-00176-i023.jpg 14-(2′,3′,5′-Trihydroxyphenyl)tetradecan-2-ol 197 μM Modified Ellman’s method Sekhar Rao et al. [43]
Shiraia sp.
Slf14
Eumycota,
Ascomycotina,
Pyrenomycetes,
Sphaeriales,
Hypocreaceae,
Shiraia
graphic file with name molecules-22-00176-i024.jpg Huperzine A 0.6 μM Modified Ellman’s method Zhu et al. [44]
Xylaria sp.
YS-02
Eumycota,
Ascomycota,
pyrenomycetes,
Sphaeriales,
Xylariaceae,
Xylaria
graphic file with name molecules-22-00176-i025.jpg Huperzine A 0.6 μM Modified Ellman’s method Su et al. [45]
Xylaria sp. Eumycota,
Ascomycota,
pyrenomycetes,
Sphaeriales,
Xylariaceae,
Xylaria
graphic file with name molecules-22-00176-i026.jpg Xyloketal A 29.9 μM Modified Ellman’s method Lin et al. [46]
graphic file with name molecules-22-00176-i027.jpg Xyloketal B 109.3 μM
graphic file with name molecules-22-00176-i028.jpg Xyloketal C 109.3 μM
graphic file with name molecules-22-00176-i029.jpg Xyloketal D 425.6 μM
Hyalodendriella sp.
Ponipodef12
Eumycota,
Ascomycotina,
Discomycetes,
Leotiales,
Leotiaceae,
Hyalodendriella
graphic file with name molecules-22-00176-i030.jpg Palmariol B (1) 115.31 µg/mL Modified Ellman’s method Meng et al. [47], Mao et al. [48]
graphic file with name molecules-22-00176-i031.jpg 4-Hydroxymellein (2) 116.05 µg/mL
graphic file with name molecules-22-00176-i032.jpg Alternariol 9-methyl ether (3) 135.52 µg/mL
graphic file with name molecules-22-00176-i033.jpg Botrallin (4) 83.70 µg/mL
Blastomyces sp. Eumycota,
Ascomycotina,
Hemiascomycetes,
Endomycetalcs,
Endomycetaccae,
Blastomyces
graphic file with name molecules-22-00176-i034.jpg Huperzine A 0.6 μM No report Ju et al. [38]
Haddowia longipes Eumycota,
Basidiomycotina,
Hymenomycetes,
Aphyllophorales,
Ganodermataceae,
Haddowia
graphic file with name molecules-22-00176-i035.jpg 11-Oxo-ganoderiol D (1)
Lanosta-8-en-7,11-dioxo-3b-acetyloxy-24,25,26-trihydroxy (2)
Lanosta-8-en-7-oxo-3b-acetyloxy-11b,24,25,26-tetrahydroxy (3)
Ganoderiol D (10)
Lanosta-8-en-7-one-3b-acetyloxy-24,25,26-trihydroxy (11)
No report Modified Ellman’s method Zhang et al. [49]
graphic file with name molecules-22-00176-i036.jpg Lanosta-7,9(11)-dien-3b-acetyloxy-24,25,26-trihydroxy (4)
Ganodermanondiol (12)
Lucidumol B (13)
graphic file with name molecules-22-00176-i037.jpg 11β-Hydroxy-lucidadiol (7)
Lucidadiol (15)
graphic file with name molecules-22-00176-i038.jpg Lucidone H (8)
lucidadone A (17)
Bacillus subtilis Bacteria,
Firmicutes,
Bacilli,
Bacillales, Bacillaceae,
Bacillus
No clear product TLC bioautography and Modified Ellman’s method Pandey et al.; Wang et al. [50,51]
Streptomyces sp.
AH-14
Phylum Actinobacteria,
Actinomycetales,
Streptomycetaceae,
Streptomyces
graphic file with name molecules-22-00176-i039.jpg Physostigmine 41 μM Modified Ellman’s method Murao and Hayashi [52]
Streptomyces sp.
LB173
Phylum Actinobacteria,
Actinomycetales,
Streptomycetaceae,
Streptomyces
graphic file with name molecules-22-00176-i040.jpg Geranylphenazinediol 2.62 μM Modified Ellman’s method Ohlendorf et al. [53]
Streptomyces lavendulae Phylum Actinobacteria,
Actinomycetales,
Streptomycetaceae,
Streptomyces
graphic file with name molecules-22-00176-i041.jpg Oxygen heterocyclic compound 7.6 μM Modified Ellman’s method Kurokawa et al. [54]
Rubrobacter radiotolerans Phylum Actinobacteria,
Rubrobacteridae,
Rubrobacterales,
Rubrobacteraceae, Rubrobacter
graphic file with name molecules-22-00176-i042.jpg 2-(2-(3-Hydroxy-1-(1H-indol-3-yl)-2-methoxypropyl)-1H-indol-3-yl)acetic acid 11.8 μM Modified Ellman’s method Li et al. [55]
graphic file with name molecules-22-00176-i043.jpg 3-(3-(2-Hydroxyethyl)-1H-indol-2-yl)-3-(1Hindol-3-yl)propane-1,2-diol 13.5 μM
N98-1021 Phylum Actinobacteria,
Actinomycetales
graphic file with name molecules-22-00176-i044.jpg Same structure as terferol 20 μM Modified Ellman’s method Dong et al. [56]
Streptosporangium sp. Phylum Actinobacteria,
Actinomycetales,
Streptomycetaceae,
Streptosporangium
graphic file with name molecules-22-00176-i045.jpg YXJ-E1
Novel compound extracted from secondary metabolites of Actinobacteria for the first time
No report Modified Ellman’s method Yang et al. [57]
graphic file with name molecules-22-00176-i046.jpg 7,4′-Dihydroxy flavone No report
Talaromyces sp. LF458 Phylum Actinobacteria,
Actinomycetales,
Arthrobacter Talaromyces
graphic file with name molecules-22-00176-i047.jpg Talaromycesone A 7.49 μM Modified Ellman’s method Wu et al. [58]
Cladonia macilenta Hoffm. Lichenes, Ascolichens,
Cladoniaceae,
Cladonia
graphic file with name molecules-22-00176-i048.jpg Biruloquinone
9,10-Phenanthrene quinone, a rare natural quinone compound
27.1 μg/mL Modified Ellman’s method Luo et al. [59]
Nostoc 78-12A Cyanophyta, Nostocales,
Nostocaceae,
Nostoc
graphic file with name molecules-22-00176-i049.jpg Nostocarboline 5.3 μM Modified Ellman’s method Becher et al. [60]