Concept explainers
(a)
To draw: The circle on isoprene unit in the astaxanthin molecule.
Introduction:
Isoprenoids are the natural occurring precursor of cholesterol and contain a huge variety. Isoprenoids are synthesized by the mevalonate pathway and are commercially and medically important. Their synthetic production is a low yielding expensive process.
Isoprenoids are the precursors of astaxanthin, which is a type of carotenoid. It appears red orange in color. It serves as a strong antioxidant that can be absorbed by humans.
(a)
Explanation of Solution
Pictorial representation: Fig.1 shows isoprene unit in astaxanthin molecule.
Fig.1: Isoprene unit in astaxanthin molecule.
Explanation:
Astaxanthin molecule is made up of eight isoprene molecules. It is a type of carotenoid which occurs in salmon, algae, shrimp, and lobster, and appears orange-red in color.
(b)
To determine: Whether two molecules of geranylgeranyl pyrophosphate are joined head to head or head to tail.
Introduction:
Phyotene is an intermediate formed during the synthesis of astaxanthin and other carotenoid molecule. Its function is to maintain the growth and development of plastids.
(b)
Explanation of Solution
Pictorial representation: Fig.2 shows the Phyotene.
Fig.2: Phyotene.
Explanation:
Phyotene molecules are formed by “head-to-head joining” of two geranylgeranyl pyrophosphate molecules, as phyotene contain dimethyl group at the tail position. The joining of two geranylgeranyl pyrophosphate molecules releases diphosphate during joining without releasing a free -OH group.
(c)
To determine: The chemical transformation during the production in step five of astaxanthin synthesis.
Introduction:
Phyotene is an intermediate formed during the synthesis of astaxanthin and other carotenoid molecule. Its function is to maintain the growth and development of plastids.
(c)
Explanation of Solution
Explanation:
In chemical transformation during fifth step, phyotene is converted into lycopene. The enzyme dehydrogenase is responsible for catalyzing the transformation reaction and it converts four single bonds into double bond.
(d)
To determine: The requirement of net oxidation for cyclization during cholesterol synthesis.
Introduction:
Cholesterol consists of four ring structure which is fused together. It contains two methyl groups which lie above the plain containing four rings. Cholesterol is a component of plasma protein and plasma membrane, and present in abundance in nerve tissues
(d)
Explanation of Solution
Explanation:
There is no requirement of net oxidation for cyclization during cholesterol synthesis as during this process, two single bonds are replaced by double bond, hence there is no oxidation or reduction.
(e)
To determine: The step in the pathway which is catalyzed by the enzyme encoded by gps gene
Introduction:
Two geranylgeranyl pyrophosphate molecules are joined together and results in the formation of phyotene. The reaction releases diphosphate during joining without releasing a free –OH group
(e)
Explanation of Solution
Explanation:
Gene gps encodes the enzyme which regulates the steps one to three in the pathway. The pathway represents the conversion of
(f)
To determine: The expression level of the enzyme which is capable of catalyzing step 3 of the astaxanthin synthesis pathway.
Introduction:
Isoprenoids are the precursors of astaxanthin, which is a type of carotenoid, and appear red orange in color. It serves as a strong antioxidant that can be absorbed by humans.
(f)
Explanation of Solution
Explanation:
The comparison of strain1 through strain 4 does not express astaxanthin, whereas strain 5 through strain 8 shows over expression of gene crtE and leads to overproduction astaxanthin.
Third step of astaxanthin involves the conversion of farnesyl pyrophosphate into geranylgeranyl pyrophosphate, in wild type E. coli strain.
(g)
To determine: The enzyme which is rate limiting in the astaxanthin synthesis pathway.
Introduction:
In the astaxanthin synthesis pathway in E. coli, enzymes are encoded by crtBIZYW, crtE, ispA and idi genes, which catalyze the pathway and yield astaxanthin. The idi encodes for IPP isomerase.
(g)
Explanation of Solution
Explanation:
The ispA gene catalyzes step one and two of the pathway in strain 5 and 6 and results in a little increase in the production of astaxanthin. idi gene catalyzes the process in the strain 7 and strain 8 and shows increase in the production of astaxanthin. Hence, the enzyme IPP isomerase catalyzes the rate limiting step of the pathway when the gene crtE is overexpressed.
(h)
To determine: Whether a strain overexpressing crtBIZYW, gps and crtE genes will produce low (+), medium (++), or high (+++) levels of astaxanthin, as measured by its orange color
Introduction:
In the astaxanthin synthesis pathway in E. coli, enzymes are encoded by crtBIZYW, crtE, ispA and idi genes, which catalyze the pathway and yield astaxanthin. Idi encodes for IPP isomerase.
(h)
Explanation of Solution
Explanation:
crtBIZYW, gps and crtE genes are expressed in strain 5, strain 6, and strain 9 and produce a low level of astaxanthin, The genes expressed in strain 7, strain 8 and strain 9 overproduces astaxanthin because of over expression of idi gene. Thus, IPP isomeraselimits the production of astaxanthin.
Want to see more full solutions like this?
Chapter 21 Solutions
Lehninger Principles of Biochemistry
- Biochemistry Question.For the metabolism of amino acids what is the first step for theirbreakdown? Why is it necessary for this breakdown product to be transported to the liver? For the catabolism of the carbon backbone of these amino acids, there are 7 entry points into the “standard” metabolic pathways. List these 7 entry points and which amino acids are metabolized to these entry points. Please help. Thank you!arrow_forwardBiochemistry Question. Please help. Thank you. You are studying pyruvate utilization in mammals for ATP production under aerobic conditions and have synthesized pyruvate with Carbon #1 labelled with radioactive C14. After only one complete cycle of the TCA cycle, which of the TCA cycle intermediates would be labeled with C14? Explain your answer. Interestingly, you find C14 being excreted in the urine. How does it get there?arrow_forwardBiochemistry question. Please help with. Thanks in advance For each of the enzymes listed below, explain what the enzyme does including function, names (or structures) of the substrate and products and the pathway(s) (if applicable) it is/are found in. (a) ATP synthetase (b) succinate dehydrogenase (c) isocitrate lyase (d) acetyl CoA carboxylase (e) isocitrate dehydrogenase (f) malate dehydrogenasearrow_forward
- Draw and name each alcohol and classify it as primary, secondary, or tertiary. Explain your answer thoroughly.arrow_forwardDraw the product of each reaction. If there are multiple products, draw only the major product. Explain your answer thoroughly.arrow_forwardIdentify the type of bond in the following disaccharides. Number your carbons to show work. Explain your answer thoroughly. Draw the number of carbons also.arrow_forward
- Draw and explain your answer thoroughly: a. What is the molar mass of aspirin (C9H8O4)?b. What is the mass of 0.00225mol of aspirin?c. How many moles of aspirin are present in 500mg of aspirin?arrow_forwardGeranylgeranyl pyrophosphate 5 is converted by general acid-base catalysis to 6, and then to the natural product 7. For clarity only limited atom numbers are shown, but the main chain carbons are numbered 1 to 16, and the off-chain methyl substituents are numbered 17-20. A. Based on what you specified in A, use curly arrows on the drawing above to convert 5 to 6, and 6 to 7. Invoke general acids and general bases as needed, and draw in hydrogens as necessary . B. On the structure of 7, write in the atom numbers for the carbons marked with an asteriskarrow_forwardα-Pinene (4) is synthesized enzymatically from nerol pyrophosphate 1. Drawn an arrow-pushing mechanism from 1 to 2 to 3 to 4; add explicit hydrogens to clarify, if needed.arrow_forward
- A reverse phase column chromatography separates proteins according to their polarity. Which pentapeptide will be eluted FIRST when chromatographed at pH 7 using a reverse phase column such as a C-18 column? Peptide Sequence (from N-terminal to C-terminal) AKGED GAAVF ALLLI MCYAG GAAVF MCYAG ALLLI AKGEDarrow_forwardMelting of three DNA samples with varying lengths was monitored by increase of ultraviolet light absorbance at 260 nm. Which is the shortest DNA? A B Carrow_forwardSelect the CORRECT description of the peptide bond. The peptide bond can freely rotate around the peptide bond. The peptide bond is non-polar, hydrophobic and does not have a dipole. The peptide bond is most stable in the cis configuration. The peptide bond is rigid and planar. The peptide bond has a mix of single and double bond characters. The peptide bond is most stable in the trans configuration.arrow_forward
- BiochemistryBiochemistryISBN:9781319114671Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.Publisher:W. H. FreemanLehninger Principles of BiochemistryBiochemistryISBN:9781464126116Author:David L. Nelson, Michael M. CoxPublisher:W. H. FreemanFundamentals of Biochemistry: Life at the Molecul...BiochemistryISBN:9781118918401Author:Donald Voet, Judith G. Voet, Charlotte W. PrattPublisher:WILEY
- BiochemistryBiochemistryISBN:9781305961135Author:Mary K. Campbell, Shawn O. Farrell, Owen M. McDougalPublisher:Cengage LearningBiochemistryBiochemistryISBN:9781305577206Author:Reginald H. Garrett, Charles M. GrishamPublisher:Cengage LearningFundamentals of General, Organic, and Biological ...BiochemistryISBN:9780134015187Author:John E. McMurry, David S. Ballantine, Carl A. Hoeger, Virginia E. PetersonPublisher:PEARSON