scholarly journals γ-Aminobutyric Acid Pathway and Modified Tricarboxylic Acid Cycle Activity During Growth and Sporulation of Bacillus thuringiensis

1975 ◽  
Vol 30 (3) ◽  
pp. 489-492 ◽  
Author(s):  
John N. Aronson ◽  
David P. Borris ◽  
Jeffrey F. Doerner ◽  
Evelyn Akers
1967 ◽  
Vol 13 (5) ◽  
pp. 521-531 ◽  
Author(s):  
T. P. T. Evelyn

Three mycobacterial strains isolated from fish degraded putrescine by a pathway in which γ-aminobutyraldehyde (Δ′-pyrroline), γ-aminobutyric acid, succinic semialdehyde, and succinic acid were intermediates. These results agree substantially with those of other workers using different microorganisms. Intact cells utilized γ-aminobutyric acid in a transaminase reaction with endogenously supplied α-ketoglutarate to produce succinic semialdehyde and glutamate. Studies with arsenite-poisoned cells showed that a significant proportion of putrescine was metabolized via pyruvate and alanine. When putrescine-1,4-14C was substrate, HCl extracts of cells contained radioactive aspartate and glutamate in addition to alanine. The further metabolism of succinate therefore proceeded in two directions: one yielding oxalacetate and α-ketoglutarate by way of the tricarboxylic acid cycle, and the other branching off the cycle to yield pyruvate. Studies with cell-free extracts suggested that putrescine nitrogen was assimilated via glutamate, which served as the amino-group donor to yield alanine and aspartate.


1977 ◽  
Vol 23 (7) ◽  
pp. 916-921 ◽  
Author(s):  
A. J. Lewis ◽  
J. D. A. Miller

Strains of two species of Desulfovibrio were examined for enzymes of the tricarboxylic acid cycle and related pathways. Pyruvate carboxylase (EC 6.4.1.1) is present, and α-ketoglutarate is formed via the tricarboxylic acids. Glutamate, but not succinyl-CoA, arises from α-ketoglutarate. A pathway exists from pyruvate by malic enzyme (EC 1.1.1.39) activity to malate, then fumarate and succinate, again with no evidence of succinyl-CoA formation. The enzymes concerned with metabolism of these dicarboxylic acids show greater activity in the strains that can grow by fumarate dismutation. Glutamate (or glutamine), α-ketoglutarate, and yeast extract repress the enzymes that metabolize the tricarboxylic acids. There appears to be no glyoxylate cycle in Desulfovibrio vulgaris or D. desulfuricans.


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