Rewiring the reductive tricarboxylic acid pathway and L-malate transport pathway of Aspergillus oryzae for overproduction of L-malate

2017 ◽  
Vol 253 ◽  
pp. 1-9 ◽  
Author(s):  
Jingjing Liu ◽  
Zhipeng Xie ◽  
Hyun-dong Shin ◽  
Jianghua Li ◽  
Guocheng Du ◽  
...  
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.


1969 ◽  
Vol 15 (7) ◽  
pp. 731-738 ◽  
Author(s):  
Howard D. McCurdy ◽  
Boen Tie Khouw

Fruiting body formation by Stigmatella brunnea is induced by Ca2+ or Mg2+ containing media deficient in amino acids. The morphology of the fruits is quite variable and the conclusion is reached that Stigmatella brunnea and Podangium erectum may be identical. The resting cells have a definite slime capsule, are heat resistant, and are induced by glycerol and therefore may be considered to be microcysts. Their arrangement in the cysts is random.For liquid culture cultivation S. brunnea requires casitone, 0.5% starch, and magnesium. Although starch and certain sugars stimulate growth, they are not used.Growth was obtained in a medium containing 17 amino acids when thiamine was supplied. On this medium, however, there was a long lag and the yield was only 60% of that on casitone medium.The results of enzyme and respiration studies are consistent with the operation of the tricarboxylic acid cycle with a complete terminal electron-transport pathway.


1996 ◽  
Vol 42 (12) ◽  
pp. 1219-1224 ◽  
Author(s):  
Nancy A. Cornick ◽  
Bin Yan ◽  
Shelton Bank ◽  
Milton J. Allison

The gram-negative anaerobe Oxalobacter formigenes, grows on oxalate as the principal carbon and energy source, but a small amount of acetate is also required for growth. Experiments were conducted to determine the distribution and the position of label in cellular amino acids from cells grown on [13C]oxalate, [13C]acetate (1-13C, 2-13C, and U-13C), and13CCO3. The labeling pattern (determined with NMR spectroscopy) of amino acids was consistent with their formation through common biosynthetic pathways. The majority of the carbons in the amino acids that are usually derived from pyruvate, oxaloacetate, α-ketoglutarate, 3-phosphoglycerate, and carbon in the aromatic amino acids were labeled by oxalate. Carbon from13CO3was assimilated primarily into amino acids expected to be derived from oxaloacetate and α-ketoglutarate. Approximately 60% of the acetate that was assimilated into amino acids was incorporated as a C2unit into proline, arginine, glutamate, and leucine. The pattern of labeling from acetate in glutamate, arginine, and proline was consistent with acetate incorporation via citrate (si)-synthase and subsequent formation of α-ketoglutarate via the first third of the tricarboxylic acid pathway. Acetate was also assimilated into amino acids derived from pyruvate and oxaloacetate, but results indicated that this incorporation was as single carbon atoms. Based on these findings, cell-free extracts were assayed for several key biosynthetic enzymes. Enzymatic activities found included glutamate dehydrogenase, phosphoenolpyruvate carboxylase, and pyruvate carboxylase. These findings are consistent with proposed biosynthetic mechanisms.Key words: oxalate, carbon flow, carbon assimilation.


1968 ◽  
Vol 108 (1) ◽  
pp. 107-119 ◽  
Author(s):  
H. J. Somerville

Cell-free extracts of Peptostreptococcus elsdenii, a strict anaerobe from the rumen, were examined for enzymes catalysing the steps in the biosynthesis from lactate of alanine, serine, aspartate and glutamate. Extracts contain the enzymes necessary for the formation of alanine from lactate via pyruvate. The presence of enzymes catalysing the interconversion of phosphoglycerate and phosphohydroxypyruvate, the transamination of the latter to phosphoserine and the cleavage of phosphoserine to serine and inorganic phosphate was demonstrated, suggesting that serine is formed via these intermediates. ‘Malic’ enzyme, malate dehydrogenase and glutamate–oxaloacetate transaminase are present in extracts and could account for aspartate formation. The extracts catalyse all of the steps of the tricarboxylic acid pathway leading from oxaloacetate plus acetate to glutamate. Together with substantive data from previous radioactive tracer studies the results provide strong evidence that these four amino acids are synthesized in this strict anaerobe by pathways closely similar to those operating in aerobic and facultatively aerobic organisms.


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