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Using synthetic biology, genetically engineer a bacterium to smell like apple. watch the following video
https://www.youtube.com/watch?v=8oHSRBZGMdM&feature=youtu.be
and then describe by specific chemical or biological name each of the three main components of your circuit. Provide references from the scientific literature for where you found details for each of three components.
Describe how an increase in the carbon dioxide levels in the blood and interstitial fluid affects the heart, blood vessels, hemoglobin dissociation curve, and the respiratory system.
Specify whether the taste of fresh water surprised you or not? Explain if your perception of coarseness change or not?
What is the rate of coagulation of naturally occurring colloids (under various pH and I scenarios)? How may the size spectrum of agglomerates change over time? How quickly do colloidal aggregates settle.
The molecular data=based tree creates a group called "Ecdysozoa". Explain what is "ecdysis" in this group?
1) Identify the articulation site that allows us to nod our head "yes". choice (A) or (B) (A) Occipital bone - axis (B) Occipital bone - atlas Identify the articulation site that allows us to rotate our head.
In a generalized transduction experiment, phages are collected from an E. coli donor strain of genotype cys+ leu+ thr+ and used to transduce a recipient of genotype cys- leu- thr-.
Create the psychometric function that you would expect if the returned echo is shifted by 90 degree relative to the outgoing pulse of the echolocating bat, Eptesicus .
Describe the movement of water through the nephron including a description of the movement of salt and countercurrent multiplication.
Explain the two consecutive splicing steps that result in removal of introns. Splicing fidelity relies on specific recognition of introns by the splicing machinery.
Describe how a Single Nuclear Polymorphism in each INTRON, EXON, and PROMOTER would negatively impact the function/product of the gene.
Determine which of the following in an enzyme that is involved in both cell cycle control and DNA repair?
How can we use what we know about this process to construct a timeline showing when various sequence changes occurred and when they lead to the modern sequences that we know today?
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