Penicillium jensenii

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Penicillium jensenii
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Fungi
Division: Ascomycota
Class: Eurotiomycetes
Order: Eurotiales
Family: Aspergillaceae
Genus: Penicillium
Species:
P. jensenii
Binomial name
Penicillium jensenii
Zalessky, K.M. 1927 [1]
Type strain
ATCC 10456, ATCC 18317, CBS 216.28, CBS 327.59, CECT 20381, DSM 2741, FAT 605, FRR 0909, FRR 3431, IFO 5747, IFO 5764, IMI 039768, IMI 068233, LCP 89.1389, MUCL 38773, NBRC 5747, NBRC 5764, NRRL 3431, NRRL 909, QM 7298, QM , Thom 5010-10, VKM F-1147 [2]
Synonyms

Penicillium rivolii,
Penicillium siemaszki,
Penicillium siemaszkoi [1]

Penicillium jensenii is an anamorph species of the genus of Penicillium which produces citrinin, griseofulvin and fumagillin. [1] [3] [4] [5] [6] [7]

Further reading

Related Research Articles

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<span class="mw-page-title-main">Terphenylquinones</span>

Terphenylquinones are fungal dyes from the group of phenyl-substituted p-benzoquinones having the following general structure.

General chemical structure of terphenylquinones

<span class="mw-page-title-main">Rugulosin</span> Chemical compound

Rugulosin is an anthraquinoid mycotoxin with the molecular formula C30H22O10 which is produced by Penicillium species. Rugulosin is hepatotoxic and is cancerogenic.

<span class="mw-page-title-main">Luteoskyrin</span> Chemical compound

Luteoskyrin is a carcinogenic mycotoxin with the molecular formula C30H22O12 which is produced by the mold Penicillium islandicum. Luteoskyrin has strong cytotoxic effects. Luteoskyrin can cause the yellow rice disease.

<span class="mw-page-title-main">Zeorin</span> Chemical compound

Zeorin is a triterpene with the molecular formula C30H52O2 which occurs in many lichens.

<span class="mw-page-title-main">Salbostatin</span> Chemical compound

Salbostatin is an antibiotic and trehalase inhibitor with the molecular formula C13H23O8. Salbostatin is produced by the bacterium Streptomyces albus.

References

  1. 1 2 3 MycoBank
  2. Straininfo of Penicillium jensenii
  3. UniProt
  4. ATCC
  5. Gerhard Eisenbrand; Peter Schreier; Alfred Hagen Meyer (2014). RÖMPP Lexikon Lebensmittelchemie (2 ed.). Georg Thieme Verlag. ISBN   3-13-179282-5.
  6. Karl Esser; Paul A. Lemke; J. W. Bennett; Heinz D. Osiewacz (2001). Stoffwechselphysiologie Industrial Applications. Springer Science & Business Media. ISBN   3-540-41583-1.
  7. V. Betina (1993). Chromatography of Mycotoxins: Techniques and Applications. Elsevier. ISBN   0-08-085862-7.