Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1976 Jun;126(3):1075–1081. doi: 10.1128/jb.126.3.1075-1081.1976

Variation in levels of enzymes related to energy metabolism in alternative developmental pathways of Blastocladiella emersonii.

O C Ingebretsen, T Sanner
PMCID: PMC233127  PMID: 181360

Abstract

The activities of phosphofructokinase (PFK), fructose diphosphatase (FDP), nicotinamide adenine dinucleotide (NAD) and NAD phosphate (NADP)-linked isocitrate dehydrogenases (IDHNAD, IDHNADP), two NAD-linked glutamate dehydrogenases (GDH1, GDH2), and isocitrate lyase were studied during the development of the two phenotypes, ordinary colorless and resistant sporangia (OC and RS plants), of water mold Blastocladiella emersonii in synchronized liquid cultures. The OC plants had a generation time of about 12 h, whereas the RS plants required 3.5 days to reach maturity. All the enzymes were present throughout the development of both phenotypes. In zoospores, PFK, FDP, and GDH2 were localized in the cytosol. The IDHNADP activity was distributed with two-thirds in the soluble and one-third in the particulate fraction. GDH1 and IDHNAD showed the same distribution and were predominantly present in the particulate fraction, presumably in the mitochondria. Isocitrate lyase was found in the particulate fraction. The enzyme levels changed considerably during development. FDP and IDHNADP varied in a parallel manner. Similarly, the three enzymes PFK, IDHNAD and GDH1 showed parallel variations. The activity patterns for all enzymes were different for the OC and RS pathways. Isocitrate lyase exhibited the largest changes in activity during development. Thus, during OC plant formation, its activity decreased by a factor of 20. GDH2 varied similarly to PFK and IDHNADP during OC plant development, whereas it behaved like isocitrate lyase during RS plant development. The ratios between anabolic and catabolic enzymes were higher in mature plants than in zoospores and higher in RS plants than in OC plants. The results indicate that the variations in the enzyme levels are secondary to the critical changes involved in the transition from one developmental pathway to the other.

Full text

PDF
1075

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. CANTINO E. C., GOLDSTEIN A. Bicarbonate-induced synthesis of polysaccharide during morphogenesis by synchronous, single-generations of blastocladiella emersonii. Arch Mikrobiol. 1961;39:43–52. doi: 10.1007/BF00406526. [DOI] [PubMed] [Google Scholar]
  2. CANTINO E. C., LOVETT J. S. NON-FILAMENTOUS AQUATIC FUNGI: MODEL SYSTEMS FOR BIOCHEMICAL STUDIES OF MORPHOLOGICAL DIFFERENTIATION. Adv Morphog. 1964;4:33–93. doi: 10.1016/b978-1-4831-9950-4.50005-9. [DOI] [PubMed] [Google Scholar]
  3. Griffin D. H. The interaction of hydrogen ion, carbon dioxide and potassium ion in controlling the formation of resistant sporangia in Blastocladiella emersonii. J Gen Microbiol. 1965 Jul;40(1):13–28. doi: 10.1099/00221287-40-1-13. [DOI] [PubMed] [Google Scholar]
  4. Ingebretsen O. C. Properties of the nicotinamide adenine dinucleotide phosphate-specific isocitrate dehydrogenase from Blastocladiella emersonii. J Bacteriol. 1975 Oct;124(1):65–72. doi: 10.1128/jb.124.1.65-72.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Ingebretsen O. C., Sanner T. Inhibitory effects of salts on the nicotinamide adenine dinucleotide specific isocitrate dehydrogenase from Blastocladiella emersonii. Arch Biochem Biophys. 1975 Feb;166(2):501–506. doi: 10.1016/0003-9861(75)90413-0. [DOI] [PubMed] [Google Scholar]
  6. Ingebretsen O. C., Sanner T. Properties of the nicotinamide adenine dinucleotide-specific isocitrate dehydrogenase from Blastocladiella emersonii. Biochim Biophys Acta. 1974 Jul 17;358(1):25–32. doi: 10.1016/0005-2744(74)90254-x. [DOI] [PubMed] [Google Scholar]
  7. Khouw B. T., McCurdy H. D. Tricarboxylic acid cycle enzymes and morphogenesis in Blastocladiella emersonii. J Bacteriol. 1969 Jul;99(1):197–205. doi: 10.1128/jb.99.1.197-205.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. LOVETT J. S., CANTINO E. C. Reversible bicarbonate-induced enzyme activity and the point of no return during morphogenesis in Blastocladiella. J Gen Microbiol. 1961 Jan;24:87–93. doi: 10.1099/00221287-24-1-87. [DOI] [PubMed] [Google Scholar]
  9. LOVETT J. S. CHEMICAL AND PHYSICAL CHARACTERIZATION OF "NUCLEAR CAPS" ISOLATED FROM BLASTOCLADIELLA ZOOSPORES. J Bacteriol. 1963 Jun;85:1235–1246. doi: 10.1128/jb.85.6.1235-1246.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  11. McCurdy H. D., Cantino E. C. Isocitritase, Glycine-Alanine Transaminase, and Development in Blastocladiella Emersonii. Plant Physiol. 1960 Jul;35(4):463–476. doi: 10.1104/pp.35.4.463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Mills G. L., Cantino E. C. Isolation and characterization of microbodies and symphyomicrobodies with different buoyant densities from the fungus Blastocladiella emersonii. Biochem Biophys Res Commun. 1975 Dec 1;67(3):1256–1263. doi: 10.1016/0006-291x(75)90808-6. [DOI] [PubMed] [Google Scholar]
  13. Myers R. B., Cantino E. C. DNA profile of the spore of Blastocladiella emersonii: evidence for -particle DNA. Arch Mikrobiol. 1971;78(3):252–267. doi: 10.1007/BF00424898. [DOI] [PubMed] [Google Scholar]
  14. Sanner T. Activation of glutamate dehydrogenase from Blastocladiella emersonii by AMP. Biochim Biophys Acta. 1971 Nov 13;250(2):297–305. doi: 10.1016/0005-2744(71)90186-0. [DOI] [PubMed] [Google Scholar]
  15. Sanner T., Ingebretsen O. C. Role of NADPH in the regulation of NADP-specific isocitrate dehydrogenase from pig heart. Arch Biochem Biophys. 1976 Jan;172(1):59–63. doi: 10.1016/0003-9861(76)90047-3. [DOI] [PubMed] [Google Scholar]
  16. Sanner T. The unidirectional inhibition of glutamate dehydrogenase from Blastocladiella emersonii. Biochim Biophys Acta. 1972 Mar 8;258(3):689–700. doi: 10.1016/0005-2744(72)90170-2. [DOI] [PubMed] [Google Scholar]
  17. Smith J. E., Galbraith J. C. Biochemical and physiological aspects of differentiation in the fungi. Adv Microb Physiol. 1971;5:45–134. doi: 10.1016/s0065-2911(08)60405-1. [DOI] [PubMed] [Google Scholar]
  18. Soll D. R., Sonneborn D. R. Zoospore germination in Blastocladiella emersonii: cell differentiation without protein synthesis? Proc Natl Acad Sci U S A. 1971 Feb;68(2):459–463. doi: 10.1073/pnas.68.2.459. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Truesdell L. C., Cantino E. C. The induction and early events of germination in the zoospore of Blastocladiella emersonii. Curr Top Dev Biol. 1971;6(6):1–44. doi: 10.1016/s0070-2153(08)60636-5. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES