Answer:
It recognizes and binds to a pair of "mismatched" nucleotides, preventing their translation.
Explanation:
Mut L protein is involved in mismatch DNA repair. MutL protein is complexed with MutS protein and the MutL-MutS complex recognizes all the mismatched base pairs present in the newly formed DNA strand. The complex can not recognize the "C-C" pairs. MutH protein joins the complex.
The MutH protein also has a site-specific endonuclease activity and cleaves the unmethylated DNA strand towards the 5' end of the guanine base in the GATC sequence to mark the strand for DNA repair. In this way, MutL protein, along with MutS and MutH proteins mark the mismatched DNA bases for repair so that they are not translated into a faulty protein.
Hi the answer to your question is Julie's grandmother has Atherosclerosis.
Hope this helps you.
A human fetus develops at the mother’s body temperature. At birth, most newborns experience a drop in temperature, and their bodies must quickly do something about it. What they do is the same thing a hibernating mammal does as it rouses itself from its winter "snooze." During hibernation, an animal’s body temperature is low. In order to move about and take care of itself once awake again, the animal that has been hibernating must raise its body temperature. (William k. Purves et al., life: the science of biology) The definition is the primary pattern of organization in this passage.
This passage is explaining the process of hibernation and its importance in the animal life cycle.
To learn more about hibernation here
brainly.com/question/2594381
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Answer:
DNA restriction enzymes cut the DNA molecule, while DNA ligases join the resulting DNA fragments
Explanation:
Transformation is a naturally occurring process by which bacteria incorporate exogenous genetic material from their surrounding environment. This process (transformation) is used for DNA cloning via plasmid vectors. In DNA cloning, transformation occurs after restriction enzymes cut the DNA at specific sequences named palindromic sequences (i.e, sequences that can be read the same in opposite direction). Restriction enzymes can generate sticky-ends, where enzymes make staggered cuts in the two strands (e.g., <em>BamH</em>), or blunt ends, where the resulting strands are of the same length (e.g., <em>HaeIII</em>). In general, sticky-end enzymes are more useful because they generate a 3' overhang in one molecule and a complementary 5' overhang in the other, increasing the yield and specificity of ligation. During ligation, a DNA ligase is used to join both DNA strands by forming phosphodiester bonds in the plasmid. Following transformation, bacteria can be selected on antibiotic plates.
Because they are the same chemical reaction but reversed. Cellular respiration takes glucose (from nutrient/food) and oxygen (from atmosphere) in order to make CO2 (think about exhaling) and H20 (water).
(I don't remember this clearly so it may be wrong, i'll look into it and come back!)
