There is 2 types of amylase. But they have to same function which is to digest starch to Maltose. They r salivary amylase and pancreatic amylase.
Salivary amylase is produced in the salivary glands, while pancreatic amylase is produced in the pancreas
Answer:
The correct answer is option e, that is, a, b and c.
Explanation:
The phenomenon by which green plants and other species converts light energy into chemical energy is termed as photosynthesis. During photosynthesis, the energy of the light is captivated and is utilized to transform carbon dioxide, water, and minerals into oxygen and energy-rich organic components.
With the transport of electron through the chloroplast membrane, the energy of the electron causes the diffusion of a hydrogen ion from stroma into the thylakoid lumen, which further leads to a formation of hydrogen ion concentration gradient. This gradient ultimately results in the formation of ATP.
Exercising will lower your blood sugar level, like brisk walking, swimming, or bike riding. Drinking water will help lower your blood sugar levels as well. Sleeping can help lower blood sugar levels too. Good luck!
Answer:
Mechanical digestion
Chemical digestion
Explanation:
Food is physically broken into smaller parts. For instance, by chewing.
Food is broken down by acids and enzymes into its basic units.
Answer:
Several 2',3'-dideoxy-3'-thiapyrimidine nucleosides were studied for their ability to inhibit hepatitis B virus (HBV) DNA replication in a HBV-transfected cell line (2.2.15). 2',3'-Dideoxy-3'-thiacytidine (SddC) and 5-fluoro-2',3'-dideoxy-3'-thiacytidine(5-FSddC) were found to be the most potent anti-HBV compounds of those examined. Both compounds resulted in nearly complete cessation of viral DNA replication at 0.5 microM, as monitored by the absence of both intracellular episomal and secreted viral DNAs. The HBV-specific RNAs were not reduced at concentrations that completely blocked HBV DNA replication, suggesting that the inhibitory target is HBV DNA synthesis. The antiviral action of SddC and 5-FSddC was reversible. The concentration of SddC and 5-FSddC required to inhibit 50% of 4-day cell growth in culture was 37 microM and more than 200 microM, respectively. Unlike 2',3'-dideoxycytidine, these two compounds do not affect mitochondrial DNA synthesis in cells at concentrations lower than that required to inhibit cell growth. In view of the potent and selective antiviral activity, both SddC and 5-FSddC should be further evaluated for the treatment of human HBV infection.
Explanation:
