Literature DB >> 5802605

Tricarboxylic acid cycle enzymes and morphogenesis in Blastocladiella emersonii.

B T Khouw, H D McCurdy.   

Abstract

During exponential growth, ordinary colorless (OC) plants of Blastocladiella emersonii consumed little glucose and produced no lactic acid. Similarly, resistant sporangial (RS) plants did not utilize glucose or produce lactic acid during the first 24 hr of exponential growth. During the next 24 hr of RS development, glucose was consumed with the concomitant production of lactic acid which was then reutilized. Lactic acid gradually accumulated again at maturity. Enzyme studies on cell-free extracts indicated the presence of all tricarboxylic cycle enzymes except alpha-ketoglutarate dehydrogenase at all stages of development of both RS and OC plants. Included among the enzymes detected were an adenosine monophosphate-stimulated, nicotinamide adenine dinucleotide-isocitric dehydrogenase, and citrate-condensing enzyme. When measured on a per plant basis, tricarboxylic cycle enzyme levels increased during the exponential growth of both kinds of plants. Only after the bicarbonate ceased to have effect on RS plant morphogenesis was there a decrease in the levels of the tricarboxylic cycle enzymes when measured on a per plant basis. Specific activity measurements indicated some differences in the differential rates of synthesis among the enzymes studied previous to 36 hr. Preliminary studies utilizing short periods of (14)C-bicarbonate fixation in young RS plants indicated that during the first 4 min most of the label was located in aspartic acid. These results are discussed in terms of previous results and particularly Cantino's hypothesis concerning the relationship between bicarbonate induction and tricarboxylic-cycle enzymes in the morphogenesis of B. emersonii.

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Year:  1969        PMID: 5802605      PMCID: PMC249987          DOI: 10.1128/jb.99.1.197-205.1969

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  15 in total

1.  A role for glycine in light stimulated nucleic acid synthesis by Blastocladiella emersonii.

Authors:  E C CANTINO; G TURIAN
Journal:  Arch Mikrobiol       Date:  1961

2.  On the mechanism of alpha-oxoglutarate oxidation in Escherichia coli.

Authors:  L P HAGER; H L KORNBERG
Journal:  Biochem J       Date:  1961-01       Impact factor: 3.857

3.  Reversible bicarbonate-induced enzyme activity and the point of no return during morphogenesis in Blastocladiella.

Authors:  J S LOVETT; E C CANTINO
Journal:  J Gen Microbiol       Date:  1961-01

4.  A colorimetric method for the assay of soluble succinic dehydrogenase and pyridinenucleotide-linked dehydrogenases.

Authors:  H A ELLS
Journal:  Arch Biochem Biophys       Date:  1959-12       Impact factor: 4.013

5.  Further evidence for the role of the tricarboxylic acid cycle in morphogenesis in Blastocladiella emersonii.

Authors:  E C CANTINO; M T HYATT
Journal:  J Bacteriol       Date:  1953-12       Impact factor: 3.490

6.  Isocitritase, Glycine-Alanine Transaminase, and Development in Blastocladiella Emersonii.

Authors:  H D McCurdy; E C Cantino
Journal:  Plant Physiol       Date:  1960-07       Impact factor: 8.340

7.  Studies on alpha-ketoglutaric oxidase. I. Formation of "active" succinate.

Authors:  D R SANADI; J W LITTLEFIELD
Journal:  J Biol Chem       Date:  1951-12       Impact factor: 5.157

Review 8.  The role of CO2 fixation in metabolism.

Authors:  H G Wood; M F Utter
Journal:  Essays Biochem       Date:  1965       Impact factor: 8.000

9.  The accumulation of alpha-ketoglutarate by suspensions of Pseudomonas aeruginosa.

Authors:  M Von Tigerstrom; J J Campbell
Journal:  Can J Microbiol       Date:  1966-10       Impact factor: 2.419

10.  CO(2) Fixation, Glutamate Labeling, and the Krebs Cycle in Ribose-grown Hydrogenomonas facilis.

Authors:  B A McFadden; G D Kuehn; H R Homann
Journal:  J Bacteriol       Date:  1967-03       Impact factor: 3.490

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  11 in total

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

Authors:  O C Ingebretsen; T Sanner
Journal:  J Bacteriol       Date:  1976-06       Impact factor: 3.490

2.  Enzymatic basis for differentiation of Rhizobium into fast- and slow-growing groups.

Authors:  G Martínez-De Drets; A Arias
Journal:  J Bacteriol       Date:  1972-01       Impact factor: 3.490

3.  Succinate dehydrogenase mutant of Rhizobium meliloti.

Authors:  A Gardiol; A Arias; C Cerveñansky; G Martínez-Drets
Journal:  J Bacteriol       Date:  1982-09       Impact factor: 3.490

4.  Organic acid metabolism in Sclerotinia sclerotiorum.

Authors:  D L Corsini; D Le Tourneau
Journal:  Arch Mikrobiol       Date:  1973-03-02

5.  Sequential metabolic events during encystment of Azobacter vinelandii.

Authors:  V M Hitchins; H L Sadoff
Journal:  J Bacteriol       Date:  1973-03       Impact factor: 3.490

6.  Lipid composition of the zoospores of Blastocladiella amersonii.

Authors:  G L Mills; E C Cantino
Journal:  J Bacteriol       Date:  1974-04       Impact factor: 3.490

7.  Morphological examination of the glycocalyces of Staphylococcus aureus strains Wiley and Smith.

Authors:  G G Caputy; J W Costerton
Journal:  Infect Immun       Date:  1982-05       Impact factor: 3.441

8.  Catabolism of carbohydrates and organic acids and expression of nitrogenase by azospirilla.

Authors:  G Martinez-Drets; M Del Gallo; C Burpee; R H Burris
Journal:  J Bacteriol       Date:  1984-07       Impact factor: 3.490

9.  Citrate-tris(hydroxymethyl)aminomethane-mediated release of outer membrane sections from the cell envelope of a deep-rough (heptose-deficient lipopolysaccharide) strain of Escherichia coli O8.

Authors:  R T Irvin; T J MacAlister; R Chan; J W Costerton
Journal:  J Bacteriol       Date:  1981-03       Impact factor: 3.490

10.  Effect of fungicides and insecticides on growth and enzyme activity of four cyanobacteria.

Authors:  Manojit Debnath; Narayan C Mandal; Samit Ray
Journal:  Indian J Microbiol       Date:  2011-08-13       Impact factor: 2.461

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