Ví dụ về việc sử dụng Protease trong Tiếng anh và bản dịch của chúng sang Tiếng việt
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Protease is one of the first choices.
These substances were modified in such a way that they fitexactly into the enzyme active site of the HIV protease.
The HIV protease cuts the viral gag-pol polyprotein into its functional subunits.
It is naturally bounded to protein in food andis released in the stomach through gastric protease and hydrochloric activity.
The commonest protease inhibitor in the blood is alpha-1 antitrypsin and its role is to protect the tissues from protease attack.
Mọi người cũng dịch
CYP3A4 inhibitors, which increase the amount of felodipine available per dose, include cimetidine, erythromycin, itraconazole, ketoconazole,HIV protease inhibitors, and grapefruit juice.[1][4].
With knowledge of the molecular structure of the protease encoded by the virus, the first protease inhibitors were designed in the early nineties;
Acid Protease is also a very useful tool in the leather and fur industry, as it softens and adds suppleness to lower grade materials, yet at the same time strengthens the root of the fur.
The nanoparticles are injected into a patientand, when they arrive at the diseased microenvironment, the local disease-associated protease will release small peptide fragments of a specific mass that act as the reporter.
The combination of two nukes plus one protease inhibitor is the only HAART to date that is supported by efficacy data from randomized studies with clinical endpoints(Hammer 1997, Cameron 1998, Stellbrink 2000).
One study of lopinavir/ritonavir(Keletra), a combination of the antivirals lopinavir and ritonavir, concluded that"no benefit was observed".[10][11]The drugs were designed to inhibit HIV from replicating by binding to the protease.
Finally, our enhanced delivery system includes D complex:a blend of the digestive aids protease and lactase for superior digestibility, ensuring maximum absorption and utilization of the nutrients in this formula.
Acid Protease consumed by the animal along with the feed, will work under the harsh condition of the stomach to hydrolyze protein into peptides and amino acids, promote digestion and absorption, and yield greater return of profit from feed.
Finally, our enhanced delivery system includes D complex:a blend of the digestive aids protease and lactase for superior digestibility, ensuring maximum absorption and utilization of the nutrients in this formula.
Acid Protease when used as an additive in high starch products such as bread, or in high protein products such as sausage, helps increase quality by modifying starch content and by enhancing the flavour and taste of the food.
In a paper published in 2015, the researchers created a mathematical model of this system, to understand several factors such as how the particles circulate in the body, how efficiently they encounter the protease, and at what rate the protease cleaves the peptides.
Telaprevir is an inhibitor of the HCV NS3/4A serine protease, necessary for the proteolytic cleavage of the HCV encoded polyprotein into mature forms of the NS4A, NS4B, NS5A and NS5B proteins and essential for viral replication.
Ultrasound alone or in combination with heat(thermosonication) or pressure(manosonication) or both heat and pressure(manothermosonication) is known as an effective method to inactivate various food enzymes such as lipoxygenase, peroxidase, and polyphenol oxidase,as well as heat-resistant lipase and protease.
Due to the absence of an extensive restriction-modification system, limited protease activity and the availability of suitable vector systems, Streptomyces lividans is the host of choice for the secretory production of heterologous proteins.
Initial identification of glecaprevir was done in a joint effort by AbbVie, Inc. and Enanta Pharmaceuticals.[5] Enanta had a Collaborative Development and License Agreement with AbbVie for the identification and development of paritaprevir and glecaprevir,two HCV NS3 and NS3/4A protease inhibitors, that lasted from October 2016 to June 2017.
It was the first-in-class NS3/4A protease inhibitor to enter clinical development and tested in human.[2] Ciluprevir is a potent competitive reversible inhibitor of NS3/4A protease from HCV genotype 1a(Ki= 0.3 nM) and 1b(Ki= 0.66 nM).
Acid Cellulase for improves animal's digestibility Strong liquefying activity alpha amylase Beta glucanase for improving animal's absorption Solid Lipase for feed Beta mannanase for feed Thermo resistantphytase for feed Thermostable Phytase for feed Protease for improving protein digestion of animals Sunson xylanase for feed.
Defective or missing C1-inhibitor permits activation of kallikrein, a protease that is responsible for liberating bradykinin from its precursor kininogen.[7][8] An excess of bradykinin leads to fluid leakage from blood vessels, causing swelling of tissues typical of HAE.
Contraindications include: atherosclerosis, Buerger's syndrome, coronary artery disease, hepatic disease, pregnancy, pruritus, Raynaud's syndrome, and renal disease.[8] It's also contraindicated if patient is taking Macrolide antibiotics(eg, erythromycin),certain HIV protease inhibitors(eg, ritonavir, nelfinavir, indinavir), certain azole antifungals(eg, ketoconazole, itraconazole, voriconazole) delavirdine, efavirenz or a 5-HT1 agonist(eg, sumatriptan).
Separase, also known as separin, is a cysteine protease responsible for triggering anaphase by hydrolysing cohesin, which is the protein responsible for binding sister chromatids during the early stage of anaphase.[5] In humans, separin is encoded by the ESPL1 gene.[6].
A key event in the final stages of blood coagulationis the conversion of fibrinogen into fibrin by the serine protease enzyme thrombin.[7] Thrombin is produced from prothrombin, by the action of an enzyme, prothrombinase(Factor Xa along with Factor Va as a cofactor), in the final states of coagulation.
Thermoresistant enzymes, such as lipase and protease that withstand ultra-high-temperature treatment and which can reduce the quality and shelf-life of heat-treated milk and other diary products can be inactivated more effectively by the simultaneous application of ultrasound, heat and pressure(MTS).
The coagulation cascade consists of a series of steps in which a protease cleaves and subsequently activates the next protease in the sequence.[1] Since each protease can activate several molecules of the next protease in the series, this biological cascade is amplified.
The mechanism of actionis thought to be through the inhibition of hyperactive protease activity that converts cathelicidin into the antimicrobial skin peptide LL-37.[9] Azelaic acid has been used for treatment of skin pigmentation including melasma and postinflammatory hyperpigmentation, particularly in those with darker skin types.
Concentrated High-Temperature α-Amylase for alcohol High-Temperature α-Amylase for alcohol Acid Protease for alcohol Concentrated Glucoamylase for alcohol Glucoamylase for alcohol industry Low Temperature alpha amylase Neutral Protease for alcohol Pectinase for alcohol industry Pullulanase for alcohol industry Xylanase for alcohol industry Neutral protease enzyme for alcohol industry Glucoamylase enzyme for ethanol industry.