(L)-(Trimethylsilyl)alanine synthesis exploiting hydroxypinanone-induced diastereoselective alkylation

Amino Acids ◽  
2013 ◽  
Vol 45 (2) ◽  
pp. 301-307 ◽  
Author(s):  
A. René ◽  
N. Vanthuyne ◽  
J. Martinez ◽  
F. Cavelier
Keyword(s):  
1977 ◽  
Vol 252 (14) ◽  
pp. 5010-5018
Author(s):  
H Taegtmeyer ◽  
M B Peterson ◽  
V V Ragavan ◽  
A G Ferguson ◽  
M Lesch

2022 ◽  
Author(s):  
Zheng Zhang ◽  
Penghui He ◽  
Shiying Hu ◽  
Yanqing Yu ◽  
Xiaoting Wang ◽  
...  

Abstract Objective: The production of some bio-chemicals affected by the cell growth. This study aimed at promoting the cell growth by overexpressing the synthesis of peptidoglycans tetrapeptide tail components to improve poly-γ-glutamic acid (γ-PGA) production. Results: L-alanine, D-alanine and D-alanyl-D-alanine are primary precursors for the synthesis of peptidoglycans. The addition of L-alanine and D-alanine significantly increased both the cell growth and production of γ-PGA. Then, several genes encoding key enzymes for L/D-alanine and D-alanyl-D-alanine biosynthesis were overexpressed respectively, including ald (encoding alanine dehydrogenase), dal (encoding alanine racemase) and ddl (encoding D-alanine ligase). The results showed that the overexpression of genes ald , dal and ddl increased the production of γ-PGA by 19.72%, 15.91% and 60.90%, and increased the microbial biomass by 15.58%, 18.34% and 49.85%, respectively. Moreover, we demonstrated that the overexpression of genes ald , dal and ddl increased γ-PGA production mainly by enhancing cell growth rather than providing more precursors. Conclusions: This work illustrated the importance of the L/D-alanine and D-alanyl-D-alanine synthesis to the cell growth and the high yield of γ-PGA, and provided an effective strategy for producing γ-PGA .


Endocrinology ◽  
1947 ◽  
Vol 41 (1) ◽  
pp. 108-109 ◽  
Author(s):  
ATTILIO CANZANELLI ◽  
RUTH GUILD ◽  
DAVID RAPPORT
Keyword(s):  

2012 ◽  
Vol 1 (8) ◽  
pp. 1079-1082 ◽  
Author(s):  
Shaodong Zhang ◽  
Leslie Dias Goncalves ◽  
Hervé Lefebvre ◽  
Martine Tessier ◽  
Brigitte Rousseau ◽  
...  

1991 ◽  
Vol 95 (3) ◽  
pp. 839-845 ◽  
Author(s):  
Estela M. Valle ◽  
Hans W. Heldt

2007 ◽  
Vol 293 (4) ◽  
pp. G838-G849 ◽  
Author(s):  
Jurandir Fernando Comar ◽  
Fumie Suzuki-Kemmelmeier ◽  
Écio Alves Nascimento ◽  
Adelar Bracht

It has been proposed that key enzymes of ureagenesis and the alanine aminotransferase activity predominate in periportal hepatocytes. However, ureagenesis from alanine, when measured in the perfused liver, did not show periportal predominance and even the release of the direct products of alanine transformation, lactate and pyruvate, was higher in perivenous cells. An alternative way of analyzing the functional distributions of alanine aminotransferase and the urea cycle along the hepatic acini would be to measure alanine and urea production from precursors such as lactate or pyruvate plus ammonia. In the present work these aspects were investigated in the bivascularly perfused rat liver. The results of the present study confirm that gluconeogenesis and the associated oxygen uptake tend to predominate in the periportal region. Alanine synthesis from lactate and pyruvate plus ammonia, however, predominated in the perivenous region. Furthermore, no predominance of ureagenesis in the periportal region was found, except for conditions of high ammonia concentrations plus oxidizing conditions induced by pyruvate. These observations corroborate the view that data on enzyme activity or expression alone cannot be extrapolated unconditionally to the living cell. The current view of the hepatic ammonia-detoxifying system proposes that the small perivenous fraction of glutamine synthesizing perivenous cells removes a minor fraction of ammonia that escapes from ureagenesis in periportal cells. However, since urea synthesis occurs at high rates in all hepatocytes with the possible exclusion of those cells not possessing carbamoyl-phosphate synthase, it is probable that ureagenesis is equally important as an ammonia-detoxifying mechanism in the perivenous region.


2010 ◽  
Vol 192 (20) ◽  
pp. 5304-5311 ◽  
Author(s):  
Sok Ho Kim ◽  
Barbara L. Schneider ◽  
Larry Reitzer

ABSTRACT Genetic analysis of alanine synthesis in the model genetic organism Escherichia coli has implicated avtA, the still uncharacterized alaA and alaB genes, and probably other genes. We identified alaA as yfbQ. We then transferred mutations in several transaminase genes into a yfbQ mutant and isolated a mutant that required alanine for optimal growth. For cells grown with carbon sources other than pyruvate, the major alanine-synthesizing transaminases are AvtA, YfbQ (AlaA), and YfdZ (which we designate AlaC). Growth with pyruvate as the carbon source and multicopy suppression suggest that several other transaminases can contribute to alanine synthesis. Expression studies showed that alanine modestly repressed avtA and yfbQ but had no effect on yfdZ. The leucine-responsive regulatory protein (Lrp) mediated control by alanine. We purified YfbQ and YfdZ and showed that both are dimers with Km s for pyruvate within the intracellular range of pyruvate concentration.


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