[Latin Name] Valerian Officinalis I.

[Specification] Velerenic acid 0.8% HPLC

[Appearance] Brown powder

Plant Part Used: Root

[Particle size] 80Mesh

[Loss on drying] ≤5.0%

[Heavy Metal] ≤10PPM

[Storage] Store in cool & dry area, keep away from the direct light and heat.

[Shelf life] 24 Months

[Package] Packed in paper-drums and two plastic-bags inside.

[Net weight] 25kgs/drum

[What is Valerian?]

Valerian root (valeriana officinalis) is derived from a plant native to Europe and Asia. The root of this plant has been used for thousands of years as a remedy for various ailments including sleep problems, digestive problems, and disorders of the nervous system, headaches, and arthritis. It is believed that valerian root has an impact on the availability of the neurotransmitter GABA in the brain.

[Function]

1. Beneficial for insomnia
2. FOR ANXIETY
3. AS A SEDATIVE
4. FOR OBSESSIVE COMPULSIVE DISORDER (OCD)
5. FOR DIGESTIVE PROBLEMS
6. FOR MIGRAINE FEADACHES
7. FOR HYPERACTIVITY AND FOCUS IN CHILDREN

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Genetic engineering of Saccharomyces cerevisiae for hyaluronic acid production

Hyaluronic acid (HA) is vital for normal growth and development of vertebrate which makes it as a commercially valuable polysaccharide in pharmaceutical and cosmetics industries. HA is synthesized by polymerization of two nucleotide sugars UDP-glucuronic acid and UDP-N-acetylglucosamine by the enzyme HA synthase (hasA). Two major genes required for the formation of HA monomers are hasB (UDP-glucose dehydrogenase) and hasD (glucosamine-phosphate acetyl transferase) respectively. Native Streptococcal species are being used for industrial scale production of HA, however, the presence of endotoxins and pathogenic factors renders it unsuitable for medical purposes. Hence, this demands for metabolic engineering of Generally Recognized As Safe (GRAS) microbes to produce HA. We have chosen Saccharomyces cerevisiae as a host for HA production due to its advantages such as lack of pathogenecity and hyaluronidase. In addition, it does not produce HA or any other polysaccharide that contains glucuronic acid due to absence of hasA and hasB. Thus, it makes S. cerevisiae a superior model system to elucidate HA biosynthesis. Jeong et.al., (2014) has demonstrated the expression of has genes from Xenopus laevis, though with low yield, in Pichia pastoris for HA production. In the current work, we have expressed X. laevis has genes in S. cerevisiae for producing medical-grade HA.

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