Oyster Peptide

Oyster peptide is a small molecular collagen peptide, it is extracted from fresh oyster or natural dried oyster by special pre-treatment and targeted bio-enzyme digestion technology at low temperature. Oyster peptide contains the trace elements (Zn, Se, etc.), oyster polysaccharides and taurine. It is widely used in food, pharmaceuticals and health care products.

Oyster peptideFig. 1 Oyster peptide

Effects of Oyster peptide

Oyster peptides are not only rich in protein, vitamins, trace elements with appropriate proportion and taurine, but also contain a variety of nutrients that marine organisms are specific. And a large number of clinical data confirm that oyster can improve the level of testosterone in male serum, regulate blood lipid, inhibit platelet aggregation, improve the symptoms of hyperglycemia, improve immunity, protect liver and promote metabolism. Here we mainly main introduce the following three effects:

  • Antithrombotic activity

It has been proved that oyster peptides, released in the SID (simulated intestinal digestion) tract, increase the APTT (activated partial thromboplastin time) and TT (thromboplastin time) for human serum clotting. In addition, Lineweaver–Burk plot analysis shows a competitive inhibition effect on thrombin. One novel peptide, LSKEEIEEAKEV, identified from oyster hydrolysates, shows a high affinity to thrombin, displaying similar characteristics to those of bivalirudin and hirudin variant-2 [1].

Peptide LSKEEIEEAKEV and hirudin variant-2 docking with thrombin at ExositeFig. 2 Peptide LSKEEIEEAKEV and hirudin variant-2 docking with thrombin at Exosite I. (a and b) The 3D model of hirudin variant-2 and peptide LSKEEIEEAKEV; (c) the 3D model of peptide LSKEEIEEAKEV docking with thrombin at Exosite I in the S1 pocket, where the yellow stick structure is the framework of peptide 1 and the ribbon structure is thrombin

  • Antioxidant and anti-inflammatory

Bingjun Qian[2] studied the antioxidant and anti-inflammatory effects of four hydrophobic peptide fractions which obtained from enzyme hydrolysates of oyster soft tissue. The results show that they exhibited the antioxidant capacity based on DPPH (2,2-diphenyl-1-picrylhydrazyl radical) scavenging capacity, FRAP (ferric reducing antioxidant power) and ORAC (oxygen radical absorbance capacity) assay in vitro. In addition, the four peptide fractions also showed anti-inflammatory activities.

  • Protective effect on testicular injury and spermatogenesis disorders

Xueyan Zhang[3] studied the mechanism of peptides from oyster on triptolide-induced testis injury in male mice. The results showed that Ops (oyster peptides) significantly improved the sperm count and motility of mice and alleviated the seminiferous tubule injury. Possible mechanism is showed below.

Possible mechanism underlying the protective effects of oyster peptides intervention on triptolide-induced
    testicular damage in mice Fig. 3 Possible mechanism underlying the protective effects of oyster peptides intervention on triptolide-induced testicular damage in mice

Alfa Chemistry supplies oyster peptide with molecular weight less than 1000Dal. which can be used in food, health care, pharmaceuticals industries. You can access to technical data for detail information. Please feel free to contact us if you have any questions.

COA

CoA
- Oyster Peptide

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TDS

TDS
- Oyster Peptide

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MSDS

MSDS
- Oyster Peptide

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References

  1. Hui Chen, Shuzhen Cheng, Fengjiao Fan, et al. Identification and molecular mechanism of antithrombotic peptides from oyster proteins released in simulated gastro-intestinal digestion. Food & Function, 2019.
  2. Bingjun Qian, Xin Zhao, Ye Yang, Chongchong Tian. Antioxidant and anti-inflammatory peptide fraction from oyster soft tissue by enzymatic hydrolysis. Food Sci Nutr. 2020;8:3947–3956.
  3. Xueyan Zhang, Zhilan Peng, Huina Zheng, et al. The Potential Protective Effect and Possible Mechanism of Peptides from Oyster (Crassostrea hongkongensis) Hydrolysate on Triptolide-Induced Testis Injury in Male Mice. Mar. Drugs 2021, 19, 566.


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