We're given the type of enzyme contained within a virus, and we're asked to make a determination of the virus' genetic makeup.

To begin with, we're told that the enzyme is an RNA-dependent RNA polymerase. The name of the enzyme gives us insight into what it does. It requires RNA as a template to produce more RNA.

So if this enzyme can convert RNA into RNA, where does the original RNA come from? The answer is that it must come from the virus. This means that we must be dealing with single-stranded RNA.

Now, the question is to determine the sense of the RNA genome of the virus. That is to say, it can be minus or plus. A minus-sense RNA is one whose complementary sequence can be translated into protein. A plus-sense RNA is one that doesn't need any processing to be translated. Rather, plus-sense RNA can be translated right away. Since we know that the enzyme present is going to produce RNA from RNA, we can then reason that the viral genome is likely minus-sense. When the minus-sense RNA is enacted on by this enzyme, the result is a new strand of RNA that can be translated into protein to serve the needs of the virus.

We're given the type of enzyme contained within a virus, and we're asked to make a determination of the virus' genetic makeup.

To begin with, we're told that the enzyme is an RNA-dependent RNA polymerase. The name of the enzyme gives us insight into what it does. It requires RNA as a template to produce more RNA.

So if this enzyme can convert RNA into RNA, where does the original RNA come from? The answer is that it must come from the virus. This means that we must be dealing with single-stranded RNA.

Now, the question is to determine the sense of the RNA genome of the virus. That is to say, it can be minus or plus. A minus-sense RNA is one whose complementary sequence can be translated into protein. A plus-sense RNA is one that doesn't need any processing to be translated. Rather, plus-sense RNA can be translated right away. Since we know that the enzyme present is going to produce RNA from RNA, we can then reason that the viral genome is likely minus-sense. When the minus-sense RNA is enacted on by this enzyme, the result is a new strand of RNA that can be translated into protein to serve the needs of the virus.

Aspartate can form arginosuccinate, which can then release a fumarate molecule. The fumarate can enter into the Krebs cycle and eventually the pathway can lead to gluconeogenesis. The arginine from the arginosuccinate can continue through the urea cycle.

Aspartate can form arginosuccinate, which can then release a fumarate molecule. The fumarate can enter into the Krebs cycle and eventually the pathway can lead to gluconeogenesis. The arginine from the arginosuccinate can continue through the urea cycle.

We're given the type of enzyme contained within a virus, and we're asked to make a determination of the virus' genetic makeup.

To begin with, we're told that the enzyme is an RNA-dependent RNA polymerase. The name of the enzyme gives us insight into what it does. It requires RNA as a template to produce more RNA.

So if this enzyme can convert RNA into RNA, where does the original RNA come from? The answer is that it must come from the virus. This means that we must be dealing with single-stranded RNA.

Now, the question is to determine the sense of the RNA genome of the virus. That is to say, it can be minus or plus. A minus-sense RNA is one whose complementary sequence can be translated into protein. A plus-sense RNA is one that doesn't need any processing to be translated. Rather, plus-sense RNA can be translated right away. Since we know that the enzyme present is going to produce RNA from RNA, we can then reason that the viral genome is likely minus-sense. When the minus-sense RNA is enacted on by this enzyme, the result is a new strand of RNA that can be translated into protein to serve the needs of the virus.

Aspartate can form arginosuccinate, which can then release a fumarate molecule. The fumarate can enter into the Krebs cycle and eventually the pathway can lead to gluconeogenesis. The arginine from the arginosuccinate can continue through the urea cycle.

In order to linearize using a linkage, there needs to be an unbound carbon on the 1 position. However, sucrose is a linkage and doesn't have a carbon available to linearize in the 1 position. It isn't a reducing sugar and therefore cannot be linearized. All of the other sugars have their anomeric carbon located at the 1 position and all of them are reducing sugars that can be linearized.

In order to linearize using a linkage, there needs to be an unbound carbon on the 1 position. However, sucrose is a linkage and doesn't have a carbon available to linearize in the 1 position. It isn't a reducing sugar and therefore cannot be linearized. All of the other sugars have their anomeric carbon located at the 1 position and all of them are reducing sugars that can be linearized.

In order to linearize using a linkage, there needs to be an unbound carbon on the 1 position. However, sucrose is a linkage and doesn't have a carbon available to linearize in the 1 position. It isn't a reducing sugar and therefore cannot be linearized. All of the other sugars have their anomeric carbon located at the 1 position and all of them are reducing sugars that can be linearized.

There are few differences between prokaryotes and eukaryotes in what concerns transcription. In prokaryotes there is only one RNA polymerase, while in eukaryotes there are three: I , II and III. In prokaryotes, both sigma factor and rho factor are required for transcription to occur, but not in eukaryotes.