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(S)-Malic acid

(S)-Malic acid
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Purity:99.86%
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(S)-Malic acid

Catalog No. T4838Cas No. 97-67-6
(S)-Malic acid ((S)-2-Hydroxysuccinic acid) is a tart-tasting organic dicarboxylic acid that plays a role in many sour or tart foods. Apples contain malic acid, which contributes to the sourness of a green apple. Malic acid can make a wine taste tart, although the amount decreases with increasing fruit ripeness. (wikipedia). In its ionized form malic acid is called malate. Malate is an intermediate of the TCA cycle along with fumarate. It can also be formed from pyruvate as one of the anaplerotic reactions. In humans, malic acid is both derived from food sources and synthesized in the body through the citric acid cycle or Krebs cycle which takes place in the mitochondria. Malate's importance to the production of energy in the body during both aerobic and anaerobic conditions is well established. Under aerobic conditions, the oxidation of malate to oxaloacetate provides reducing equivalents to the mitochondria through the malate-aspartate redox shuttle. During anaerobic conditions, where a buildup of excess of reducing equivalents inhibits glycolysis, malic acid's simultaneous reduction to succinate and oxidation to oxaloacetate is capable of removing the accumulating reducing equivalents. This allows malic acid to reverse hypoxia's inhibition of glycolysis and energy production. In studies on rats it has been found that only tissue malate is depleted following exhaustive physical activity. Other key metabolites from the citric acid cycle needed for energy production were found to be unchanged. Because of this, a deficiency of malic acid has been hypothesized to be a major cause of physical exhaustion. Notably, the administration of malic acid to rats has been shown to elevate mitochondrial malate and increase mitochondrial respiration and energy production.
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Pack SizePriceAvailabilityQuantity
5 g$29In Stock
10 g$34In Stock
1 mL x 10 mM (in DMSO)$29In Stock
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Product Introduction

Bioactivity
Description
(S)-Malic acid ((S)-2-Hydroxysuccinic acid) is a tart-tasting organic dicarboxylic acid that plays a role in many sour or tart foods. Apples contain malic acid, which contributes to the sourness of a green apple. Malic acid can make a wine taste tart, although the amount decreases with increasing fruit ripeness. (wikipedia). In its ionized form malic acid is called malate. Malate is an intermediate of the TCA cycle along with fumarate. It can also be formed from pyruvate as one of the anaplerotic reactions. In humans, malic acid is both derived from food sources and synthesized in the body through the citric acid cycle or Krebs cycle which takes place in the mitochondria. Malate's importance to the production of energy in the body during both aerobic and anaerobic conditions is well established. Under aerobic conditions, the oxidation of malate to oxaloacetate provides reducing equivalents to the mitochondria through the malate-aspartate redox shuttle. During anaerobic conditions, where a buildup of excess of reducing equivalents inhibits glycolysis, malic acid's simultaneous reduction to succinate and oxidation to oxaloacetate is capable of removing the accumulating reducing equivalents. This allows malic acid to reverse hypoxia's inhibition of glycolysis and energy production. In studies on rats it has been found that only tissue malate is depleted following exhaustive physical activity. Other key metabolites from the citric acid cycle needed for energy production were found to be unchanged. Because of this, a deficiency of malic acid has been hypothesized to be a major cause of physical exhaustion. Notably, the administration of malic acid to rats has been shown to elevate mitochondrial malate and increase mitochondrial respiration and energy production.
In vitro
Research indicates that ME plays a crucial role in the metabolism of (S)-2-Hydroxysuccinic acid (L-malic acid) by L. casei. Removing either the histidine kinase gene or the response regulator gene of the TC system eliminates the organism's capacity to metabolize (S)-2-Hydroxysuccinic acid. This outcome underscores the TC system's pivotal regulatory role and its necessity for ME expression to facilitate (S)-2-Hydroxysuccinic acid utilization. Additionally, transcriptional analysis reveals that the presence of (S)-2-Hydroxysuccinic acid triggers maeE expression and inhibits it in the presence of glucose. Conversely, TC system expression is upregulated by (S)-2-Hydroxysuccinic acid without being inhibited by glucose, highlighting distinct regulatory mechanisms for ME and the TC system in response to (S)-2-Hydroxysuccinic acid and glucose.
AliasL-(-)-Malic acid, (S)-(-)-HYDROXYSUCCINIC ACID, (S)-2-Hydroxysuccinic acid
Chemical Properties
Molecular Weight134.09
FormulaC4H6O5
Cas No.97-67-6
Storage & Solubility Information
Storage Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 27.5 mg/mL (205.09 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM7.4577 mL37.2884 mL74.5768 mL372.8839 mL
5 mM1.4915 mL7.4577 mL14.9154 mL74.5768 mL
10 mM0.7458 mL3.7288 mL7.4577 mL37.2884 mL
20 mM0.3729 mL1.8644 mL3.7288 mL18.6442 mL
50 mM0.1492 mL0.7458 mL1.4915 mL7.4577 mL
100 mM0.0746 mL0.3729 mL0.7458 mL3.7288 mL

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