Studying animals in the wild is considered somewhat experimentally out of control because of several reasons.
<u>Explanation:</u>
Study of wild animals can be done using several methods but none will be as effective as studying captivated animals. Using stationary cameras is a method to observe animals in the wild. The stationary nature of the camera makes it necessary for the animals to appear within the field of the camera.
This is difficult in places of low animal density. In addition to that placing camera at a longer distance to watch a larger area decreases the resolution of the images. When it comes to shallow water systems, the field imagery used to track the aquatic species frequently gets affected by issues like sun flicker.
Unmanned aerial vehicles can also be used to track and study animals in the wild. This is good alternative but filming through dense canopies or turbid water is a limitation. Bio loggers can also be used for animal tracking but it is limited by weight since it has to be carried by animals.
Answer:
Cysteine
Explanation:
<u>Determine the Amino acid that is primarily involved in Binding </u>
The Amino acid that is primarily involved in Binding is Cysteine. while the other Amino acid ( i.e. Histidine ) will be involved in Catalysis.
since the enzyme is functional at pH 6 to 8. and Cysteine has a pH of 5, it should be deprotonated and used primarily for Binding .
Answer: DNA is a molecule made up of two strands, twisted around each other in a double helix shape. The two strands are complementary which have a 5 prime end and a 3 prime end. To understand this question you must first understand the steps that follow.
DNA Replication:
<u>Step one: </u>
DNA Helicase (unzips) separates the strands.
<u>Step two:</u>
DNA Primase starts the process and makes a small piece of RNA called a primer. This marks the starting point for the DNA.
<u>Step three:</u>
DNA Polymerase binds to the primer and will make the new strand of DNA. DNA Polymerase can only add DNA bases in one direction, from the 5 prime end to the 3 prime end.
- The leading strand is made continuously.
- The lagging strand does not run continuously because it runs in the opposite direction. Each fragment is started with an RNA primer. DNA Polymerase then adds a short row of DNA bases from the 5 prime to 3 prime direction. This results in okazaki fragments because it can only replicate in small chunks. The process is repeated.
<u>Step four:</u>
Once the new DNA is complete the enzyme exonuclease removes all the RNA primers from both strands of DNA.
<u>Step five:</u>
Another DNA Polymerase fills in the gaps that are left behind with DNA.
<u>Step six:</u>
DNA Ligase seals up the fragments in DNA, in both strands to make a continuous double strand.
<u>Final answer:</u>
DNA Replication cannot replicate at the same time due to the leading and lagging strand.
Good luck!
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