Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:3.1.3.1 (alkaline phosphatase)
 47,916 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

L-Malate repressed sporulation in the wild-type strain of Bacillus subtilis. When 75 mM L-malate was added to the growth medium at the time of inoculation, the appearance of heat-resistant spores was delayed 6 to 8 h. The synthesis of extracellular serine protease, alkaline phosphatase, glucose dehydrogenase, and dipicolinic acid was similarly delayed. Sporulation was not repressed when malate was added to the culture at t4 or later. A mutant was selected for ability to sporulate in the presence of malate. This strain could also sporulate in the presence of glucose. The malate-resistant mutant grew poorly with malate as sole carbon source, although it possessed an intact citric acid cycle, and it showed increased levels of malic enzyme. This indicates a defect in the metabolism of malate in the mutant. A mutant lacking malate dehydrogenase activity was also able to sporulate in the presence of malate. A model for the regulation of sporulation by malate is presented and discussed. Citric acid cycle intermediates other than malate did not affect sporulation. In contrast to previous results, sporulation of certain citric acid cycle mutants could be greatly increased or completely restored by the addition of intermediates after the enzymatic block. The results indicate that the failure of citric acid cycle mutants to sporulate can be adequately explained by lack of energy and lack of glutamate.
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PMID:Repression of sporulation in Bacillus subtilis by L-malate. 81 66

The plains mouse has large seminal vesicles, coagulating glands, and dorsal and ventral prostates, whereas in the hopping mouse the only large accessory sex gland is the ventral prostate. Fructose concentration was found to be high in the coagulating glands and dorsal prostate of the plains mouse, but low in all other glands of both species; low concentrations of glucose were found in all glands. Citric acid concentration was high in the dorsal prostate of the plains mouse and ventral prostate of the hopping mouse. Acid and alkaline phosphatase activities were low in all glands of both species. In castrated hopping mice, enlargement of vestigial glands could not be induced with high doses of exogenous testosterone, although there was increased secretory activity of the seminal vesicle epithelial cells.
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PMID:Biochemistry of male accessory organs of conilurine rodents. 724 71

Citric acid (CA) was used in a thermally induced phase separation (TIPS) process to improve the surface hydrophilicity and cell affinity of PLLA nano-fibrous scaffolds. The evolution of architecture, structure and physicochemical properties of the scaffold after modification has been investigated. Cell viability, adhesion, proliferation and osteogenic differentiation were characterized to evaluate the cytocompatibility and biological properties of PLLA nano-fibrous scaffolds. Citric acid interacted with PLLA through hydrogen bond association and the introduction of strong polar groups (-COOH) on the PLLA surface improved its hydrophilicity with the contact angle decreasing to a suitable range for cell adhesion and spreading. The cell exhibited extensive spreading on the CA modified PLLA scaffolds with many cellular protrusions interacting with nanofibers. Furthermore, such a modification significantly increased the cell proliferation rate, enhanced the alkaline phosphatase (ALP) activity and bone-related gene expression (ALP, OCN, COL I and Runx2) of mBMSCs along with cell development. The results demonstrate a promising modification method to promote applications of PLLA-based scaffolds.
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PMID:Citric acid modification of PLLA nano-fibrous scaffolds to enhance cellular adhesion, proliferation and osteogenic differentiation. 3226 5