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A Complement Inhibitor Produced by Stachybotrys complementi, nov. sp. K‐76, a New Species of Fungi Imperfecti

Miyazaki W, Tamaoka H, Shinohara M +6 more1980Microbiology and ImmunologyJournal Article
10.1111/j.1348-0421.1980.tb02914.xPubMed
Immune/Innate
Indoor Mold (Stachybotrys, Aspergillus, etc.)

Abstract

AbstractA complement inhibitor, K‐76, was isolated and purified from the culture supernatant of a fungus, Stachybotrys complementi, nov. sp. K‐76, isolated from soil of Ishigaki Island, Okinawa. K‐76 is a sesquiterpene compound and it can be oxidized to a monocarboxylic derivative (K‐76 COOH), the sodium salt of which is very soluble and much less toxic than K‐76. K‐76 and K‐76 COOH both inhibited complement activation by either the classical or alternative pathway. They inhibited generation of the factor chemotactic to human polymorphonuclear leukocytes from human serum by aggregated immunoglobulin. When sensitized erythrocytes were treated with complement in the presence of K‐76 COOH, the resulting unlysed cells were found to be in the state of EAC1, 4b, 2a, 3b. Thus K‐76 COOH is considered to block mainly the C5 intermediate step. K‐76 COOH did not inhibit any proteases or esterases tested, except when tested at high concentration.

Cited By (8)

  • Detection of AirborneStachybotrys chartarumMacrocyclic Trichothecene Mycotoxins on Particulates Smaller than ConidiaApplied and Environmental Microbiology · 2005
  • Effects of Intranasal Exposure to Spores of Stachybotrys atra in MiceToxicological Sciences · 1997
  • Indoor Mold, Toxigenic Fungi, andStachybotrys chartarum: Infectious Disease PerspectiveClinical Microbiology Reviews · 2003
  • Overview of investigations into pulmonary hemorrhage among infants in Cleveland, OhioEnvironmental Health Perspectives · 1999
  • A Chemically Defined Medium That Supports Mycotoxin Production by Stachybotrys chartarum Enabled Analysis of the Impact of Nitrogen and Carbon Sources on the Biosynthesis of Macrocyclic Trichothecenes and StachybotrylactamApplied and Environmental Microbiology · 2023
  • Synthesis and complement inhibitory activity of B/C/D-ring analogues of the fungal metabolite 6,7-diformyl- 3’,4’,4a’,5’,6’,7’,8’,8a’-octahydro-4,6’,7’-trihydroxy-2’,5’,5’,8a’- tetramethylspiro[1’(2’H)-naphthalene-2(3H)-benzofuran]Journal of Medicinal Chemistry · 2003

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  • References (1)

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