Hello there,
Your correct answer would be "<span>Increased surface area, Increased output".
I researched this up for you. I wanted to provide and good and fair answer.
Hope this help's.
~Jurgen</span>
Answer:
A
Explanation:
The components of salt water are chemically combined together and looks throughout, forming a homogeneous mixture.
The <u>vesicles</u> pick up whole and partial neurotransmitters from the synaptic gap and bring them into the terminal button, where other structures recycle these neurotransmitters for future use.
Within the presynaptic terminals is where the synthesis of the small-molecule neurotransmitters takes place. A process known as slow axonal transport is responsible for moving enzymes from the neuronal cell body to the cytoplasm of nerve terminals at a rate of 0.5–5 millimetres each day. These enzymes are necessary for the production of transmitters and are produced in the neuronal cell body. Transporter proteins, which are typically located in the plasma membrane of the nerve terminal, are the ones responsible for bringing the precursor chemicals that these synthetic enzymes use into the terminal. Enzymes produce a neurotransmitter pool in the cytoplasm, which must then be loaded into synaptic vesicles using transport proteins in the vesicular membrane. Within the synaptic vesicles, the final synthetic steps of the production of certain small-molecule neurotransmitters are actually carried out.
Learn more about neurotransmitters here :
brainly.com/question/1869120
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Answer and Explanation:
Ribosomes are the primary structure for protein synthesis. They can be found in the rough endoplasmic reticulum or floating in the cytosol.
Free ribosomes are not attached to any cytoplasmic structure or organelle. They synthesize proteins only for internal cell use. Other ribosomes are attached to the membrane of the endoplasmic reticulum and they are in charge of synthesizing membrane proteins or exportation proteins. Free and attached ribosomes are identical and they can alternate their location. This means that although free ribosomes are floating in the cytosol, eventually, they can get attached to the endoplasmic reticulum membrane.
Synthesis of proteins that are destined to membrane or exportation starts in the cytoplasm with the production of a molecule portion known as a <u>signal aminoacidic sequence</u>. This signal sequence varies between 13 and 36 amino acids, is located in the <u>amino extreme</u> of the synthesizing protein, and when it reaches a certain length, it meets the <u>signal recognizing particle</u>. This particle joins the signal sequence of the protein and leads the synthesizing protein and associated ribosome to a specific region in the Rough endoplasmic reticulum where it continues the protein building. When they reach the membrane of the endoplasmic reticulum, the signal recognizing particle links to a receptor associated with a pore. Meanwhile, the ribosome keeps synthesizing the protein, and the enlarged polypeptidic chain goes forward the reticulum lumen through the pore. While this is happening, another enzyme cuts the signal sequence, an action that requires energy from the ATP hydrolysis. When the new protein synthesis is complete, the polypeptide is released into the reticulum lumen. Here it also happens the protein folding (which is possible by the formation of disulfide bridges of proteins are formed) and the initial stages of glycosylation (the oligosaccharide addition).
Once membrane proteins are folded in the interior of the endoplasmic reticulum, they are packaged into vesicles and sent to the Golgi complex, where it occurs the final association of carbohydrates with proteins. The Golgi complex sends proteins to their different destinies. Proteins destined to a certain place are packaged all together in the same vesicle and sent to the target organelle. In the case of membrane proteins, they are packaged in vesicles and sent to the cell membrane where they get incrusted.
There are certain signal sequences in the <u>carboxy-terminal extreme</u> of the protein that plays an important role during the transport of membrane proteins. A signal as simple as one amino acid in the c-terminal extreme is responsible for the correct transport of the molecule through the whole traject until it reaches the membrane.
Answer:
Parapatric speciation
Explanation:
There are different types of speciation. Parapatric speciation consists of new species evolving from a continuous distribution. That is, there is no physical barrier that might impede the gene flow, in fact, it might continue during the speciation process.
There is an environmental gradient that determines different phenotypes for different environmental conditions. One phenotype is more adapted to one of the distribution extremes than the other phenotype. In the exposed case, the environmental gradient is given by the differences in pH.
In the border between the environmental extremes, there is the primary hybrid zone, where both phenotypic forms might meet and hybridize.
