Here are some frequently asked questions about L-Malic Acid, including its effects, specific uses, and safety. If you don't find the answer you're looking for, feel free to reach out to us.
A: L-Isoleucine is an essential amino acid crucial for protein synthesis and various metabolic processes.
A: L-Isoleucine supplementation may support muscle growth, energy production, immune function, and metabolic health.
A: Yes, L-Isoleucine is popular in sports nutrition formulations due to its role in muscle repair and energy metabolism.
A: Our L-Isoleucine is meticulously sourced, rigorously tested for purity and potency, and manufactured using state-of-the-art processes to ensure the highest quality standards.
A: Yes, L-Isoleucine is suitable for vegans and vegetarians as it can be derived from plant-based sources or produced through fermentation processes.
A: Some research suggests that L-Isoleucine supplementation may help regulate glucose and lipid metabolism, making it potentially beneficial for individuals with metabolic disorders.
A: L-Isoleucine supplementation is generally well-tolerated, but high doses may cause gastrointestinal discomfort in some individuals.
A: L-Isoleucine can be incorporated into various formulations such as protein powders, nutritional supplements, sports drinks, and functional foods to enhance their nutritional profile and efficacy.
A: A. Absolutely! L-Isoleucine is often utilized in cosmetic formulations for its moisturizing and rejuvenating properties.
A: A. L-Isoleucine is believed to have a positive impact on mental focus and cognition, making it a popular ingredient in certain brain health supplements.
A: A. Yes, our L-Isoleucine Chemical Ingredients are derived from non-GMO sources, ensuring the highest quality and purity.
Apart from β-ketothiolase deficiency (McKusick 203750), no genetic anomalies related to L-isoleucine degradation have been documented in humans. A 4-month-old boy, exhibiting mild hypoglycemia, lethargy, and apnea, underwent routine metabolic testing revealing elevated plasma short-chain acylcarnitines (AC) using standard methods. Analysis via tandem mass spectrometry detected heightened levels of five-carbon species in plasma AC, comprising a combination of isovaleryl and/or 2-methylbutyrylcarnitine, with no differentiation possible between the isomers using this technique. Subsequent separation methods confirmed 2-methylbutyrylcarnitine (2-MBC) as the predominant species. Routine urine analysis of the proband consistently showed elevated levels of 2-methylbutyrylglycine (2-MBG) without other diagnostic irregularities. These findings point towards an isolated deficiency in 2-methylbutyryl-CoA dehydrogenase (2-MBCDase). The schematic representation below illustrates the catabolic pathway for L-isoleucine metabolism, with the proband's defect denoted by a cross-hatched box. The numbered reactions encompass: 1. Branched-chain 2-oxyacid dehydrogenase; 2. 2-methylbutyryl-CoA dehydrogenase; 3. β-ketothiolase.
2-Methylbutyryl-Coenzyme A Dehydrogenase Deficiency: A New Inborn Error of L-Isoleucine Metabolism (K Michael Gibson, et al., 2000)