Literature DB >> 7808511

Possible relationship of succinate dehydrogenase and fatty acid synthetase activities to Aspergillus parasiticus (NRRL 5139) growth and aflatoxin production.

C L Reding1, M A Harrison.   

Abstract

Fatty acid synthetase (FAS) activity measured over time corresponded to aflatoxin B1 biosynthesis by Aspergillus parasiticus grown in minimal salts sucrose medium. Succinate dehydrogenase (SDH) activity, our primary metabolism indicator, decreased as FAS activity increased demonstrating that as primary metabolism slows, secondary metabolism and subsequently aflatoxin production begins. Fungal biomass, as measured by chitin, increased up to day 13 then stabilized. Calcium, potassium, magnesium, manganese, zinc, and a combination of these minerals were tested to determine their effect in culture on FAS and SDH activities. Cultures grown in broth supplemented with zinc had greater FAS activity and produced more aflatoxin B1 when compared to the unsupplemented control. To determine if enzyme activity in a complex substrate is altered due to mineral composition, peanuts were cultivated with gypsum (calcium sulfate) supplementation. The peanuts grown had higher calcium content but less zinc. All peanuts grown in gypsum treated fields had less aflatoxin produced on them when compared to unsupplemented peanuts. Also, FAS activity was lower and chitin content was less when compared to the unsupplemented control peanuts. The FAS activity observed in these experiments indirectly suggests that the FAS complex may be responsible for producing the precursor for aflatoxin synthesis. However, additional information is needed to validate this hypothesis.

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Year:  1994        PMID: 7808511     DOI: 10.1007/bf01102918

Source DB:  PubMed          Journal:  Mycopathologia        ISSN: 0301-486X            Impact factor:   2.574


  12 in total

1.  Intermediary metabolism and antibiotic synthesis.

Authors:  J D BU'LOCK
Journal:  Adv Appl Microbiol       Date:  1961       Impact factor: 5.086

2.  Rapid method for preparing cell-free extracts of Aspergillus ochraceus.

Authors:  G A Sansing; N D Davis; U L Diener
Journal:  Appl Microbiol       Date:  1975-02

3.  Sodium bicarbonate reduces viability and alters aflatoxin distribution of Aspergillus parasiticus in Czapek's agar.

Authors:  T J Montville; P K Goldstein
Journal:  Appl Environ Microbiol       Date:  1987-10       Impact factor: 4.792

Review 4.  Biosynthesis of aflatoxins.

Authors:  K K Maggon; S K Gupta; T A Venkitasubramanian
Journal:  Bacteriol Rev       Date:  1977-12

5.  Interconversion of aflatoxin B1 and aflatoxicol by several fungi.

Authors:  M Nakazato; S Morozumi; K Saito; K Fujinuma; T Nishima; N Kasai
Journal:  Appl Environ Microbiol       Date:  1990-05       Impact factor: 4.792

Review 6.  Enzymes and aflatoxin biosynthesis.

Authors:  M F Dutton
Journal:  Microbiol Rev       Date:  1988-06

7.  Purification and characterization of glucose-6-phosphate dehydrogenase from Aspergillus parasiticus.

Authors:  W G Niehaus; R P Dilts
Journal:  Arch Biochem Biophys       Date:  1984-01       Impact factor: 4.013

8.  Effect of Zinc on tricarboxylic acid cycle intermediates and enzymes in relation to aflatoxin biosynthesis.

Authors:  S K Gupta; K K Maggon; T A Venkitasubramanian
Journal:  J Gen Microbiol       Date:  1977-03

9.  Nitrate induces enzymes of the mannitol cycle and suppresses versicolorin synthesis in Aspergillus parasiticus.

Authors:  W G Niehaus; W P Jiang
Journal:  Mycopathologia       Date:  1989-09       Impact factor: 2.574

10.  Characterization of a succinate dehydrogenase complex solubilized from the cytoplasmic membrane of Bacillus subtilis with the nonionic detergent Triton X-100.

Authors:  L Hederstedt; E Holmgren; L Rutberg
Journal:  J Bacteriol       Date:  1979-05       Impact factor: 3.490

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