Diana Goh

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  • Diana Goh
    Participant

    A-Level Biology Tuition Singapore/H2 Biology Tuition/JC Biology Tutor

    J2 Biology Class 3.30pm-5.30pm 2/2/2013
    In today’s class we transited to the the second part of Nervous Control, touching on the tranmission of nervous impulse from one neuron to the next, which is otherwise termed β€œsynaptic transmission”. We played the game of Synaptic Tag where Norman and Rachel acted as the acetylcholinesterase enzymes in the synaptic cleft, while Srija Daphne and Thomas acted as the vesicles containing neurotransmitters acetylcholine in the presynaptic knob. The rest of class acted as the receptors on the surface of the post-synaptic neuron. As the depolarisation reached the presynaptic membrane, the vesicles started to throw out huge amounts of neurotransmitters (we used paper balls!) and a competition between acetylcholinesterase enzymes and its substrate acetylcholine resulted in very few acetylcholine molecules getting to the receptors.

    We concluded the lesson with 10 mcq questions from our MCQ assignment for this chapter, as well as the description table of synaptic neurotransmission. Homework for this week is to complete MCQ as well as Assignment 1.

    NOTE: NEXT WEEK’S LESSON WILL BE FROM 9-11AM AS IT FALLS ON CNY EVE, AND THE CENTRE CLOSES EARLY FOR REUNION DINNER. πŸ™‚

    J1 Biology Class 3.30pm-5.30pm 26/1/2013
    Today the J1 class completed the assignment for Biological molecules, rounding up the chapter. We will move on the Cell Organelles and Function as well as the Plasma Membrane next! Homework: to complete last question of biological molecules assignment and read up on the next chapter!

    NOTE: NO LESSON NEXT WEEK. SUBSEQUENT TWO LESSONS WILL BE EXTENDED BY 1HOUR EACH. πŸ™‚

    Ms Goh

    Diana Goh
    Participant

    A-Level Biology Tuition Singapore/H2 Biology Tuition/JC Biology Tutor

    J2 Biology Class 3.30pm-5.30pm 26/1/2013
    Today we had a fun lesson on a challenging topic of Nervous Control. We learned about the organisation of the nervous system, the structure of the neuron, before we dwelved into the mechanics of nervous impulse/action potential transmission along the neuron. Next week we will transit into the second part of this chapter, touching on the tranmission of nervous impulse from one neuron to the next, which is otherwise termed “synaptic transmission”. It will be another lesson taught with activities and games so do look forward! πŸ™‚

    J1 Biology Class 3.30pm-5.30pm 26/1/2013
    Today the J1 class completed the section on carbohydrates, proteins and also lipids. In other words, we completed the theory part of the entire first chapter of Biological molecules. The class has been told to complete the mcq and structured assignments for this chapter and next week we will review these assignments as a closure to this topic.

    Here’s a video on Action Potentials tranmission along an unmyelinated neuron, enjoy!
    http://highered.mcgraw-hill.com/sites/0072943696/student_view0/chapter8/animation__action_potential_propagation_in_an_unmyelinated_axon__quiz_2_.html

    Ms Goh

    Diana Goh
    Participant

    A-Level Biology Tuition Singapore/H2 Biology Tuition/JC Biology Tutor

    J2 Biology Class 3.30pm-5.30pm 19/1/2013
    Today the J2s finished the Endocrine control 2nd assignment. It was badly done and most of the pitfalls lie in answering techniques and understanding of what the question wants from them. We will move on to a theory lesson on Nervous System next week. It’s the start of a brand new chapter, so if you are bringing your friends along, come next week! πŸ™‚

    J1 Biology Class 3.30pm-5.30pm 19/1/2013
    Today is the first lesson of this year’s JC1 biology class. We went through the administrative matters regarding the syllabus outline and assessment formats as well as recommended texts for further reading. This lesson, we also managed to complete the first part (Carbohydrates) of the first Chapter on Biological Molecules. Next week we would do the second part (Proteins) and the third (Lipids).

    Good news is that there is finally no homework this week for both classes! Only for this week πŸ˜‰ Stay tuned!

    Ms Goh

    Diana Goh
    Participant

    A-Level Biology Tuition Singapore/H2 Biology Tuition/JC Biology Tutor

    J2 Class 3.30pm-5.30pm 18/8/2012
    Finished teaching Evolution. Went through Assignment 1 together in class.
    Homework is to complete last question of Assignment 1 as well as the whole of Assignment 2 and 3.
    Next week (25/8): Review Assignments 2 and 3

    Nextnext week (2/9): Isolating, Cloning and Sequencing DNA

    J1 Class 5.30pm-7.30pm 18/8/2012
    Lecture on Genetics of Bacteria
    Homework is to complete Genetics of Bacteria Assignments 1 and 2
    Nextweek (25/8): To review Virus assignment, and Bacteria assignments

    Nextnext week (2/9): Organisation and Control of Prokaryotic and Eukaryotic Genomes

    Ms Diana Goh

    Diana Goh
    Participant

    A-Level Biology Tuition Singapore/H2 Biology Tuition/JC Biology Tutor

    J2 Class Sat 3.30pm – 5.30pm 11/8/2012
    Class for today: Lecture on Diversity and Evolution, Parts 1,2,4,5
    Homework: To complete assignment 1 as well as Evolution MCQ
    Next week: Lecture on Diversity and Evolution, Part 3. Review MCQ and assignment 1 in class.

    J1 Class 5.30pm – 7.30pm 11/8/2012
    Today we completed the lecture on Genetics of viruses, and also finished up the MCQ questions as well as assignment for this chapter. Reviewed the answers for MCQs as well.
    Homework: To read up on Genetics of Bacteria, notes have already been distributed.
    Next week: Review Virus assignment, Lecture on Genetics of Bacteria

    Cheers
    Ms Goh

    Diana Goh
    Participant

    A-Level Biology Tuition Singapore/H2 Biology Tuition/JC Biology Tutor

    J2 Class Sat 3.30pm – 5.30pm 14/7/2012
    Nervous system assignment 1 is completed. Nervous system essay is completed too. MCQ and assignment 2 will be gone through next lesson during the first 40 minutes. The rest of the next lesson will be a lecture on Genetic Basis for Variation.

    J1 Class 5.30pm – 7.30pm 14/7/2012
    Completed Cell Division assignment 1. MCQ and assignment 2 will be gone through next lesson. The rest of the next lesson will be dedicated to a lecture on Cancer.

    Cheers
    Ms Diana Goh

    Diana Goh
    Participant

    A-Level Biology Tuition Singapore/H2 Biology Tuition/JC Biology Tutor

    J2 Class 3.30pm-5.30pm 23/6/2012
    Lecture on Nervous System

    J1 Class 5.30pm-7.30pm 23/6/2012
    Completed DNA and Genomics assignments 1 and 2
    Class assignment on DNA and Genomics part 3
    To read Cell Division in advance for next week!

    Ms Diana Goh

    Diana Goh
    Participant

    A-Level Biology Tuition Singapore/H2 Biology Tuition/JC Biology Tutor

    J2 Class 3.30pm-5.30pm 2/6/2012
    Lecture on Homeostasis and the Endocrine system
    Homework is assignment 1 due next lesson.

    J1 Class 5.30pm-7.30pm 2/6/2012
    Lecture on DNA and genomics part 1, on structure and roles of DNA and RNA
    Lecture on DNA and genomics part 2, on semi-conservative replication
    Homework due next lesson are the three selected questions from Assignments 1, 2 and 3.

    Ms Diana Goh

    Diana Goh
    Participant

    A-Level Biology Tuition Singapore/H2 Biology Tuition/JC Biology Tutor

    J1 Class 9-11am 26/5/2012
    Today we finished up our lecture on Enzymes. Homework is to complete MCQ as well as Enzymes assignment 1.

    J2 Class 3.30-5.30pm 26/5/2012
    DNA and Genomics part 1
    DNA and Genomics part 2
    Homework is to complete DNA and genomics assignment 1, due next lesson!

    J1 Class 5.30-7.30pm 26/5/2012
    Enzymes assignment 1 completed and gone through, we are left with just the last page to be covered next lesson. Homework is to complete assignment 2.

    Ms Diana Goh

    Diana Goh
    Participant

    A-Level Biology Tuition Singapore/H2 Biology Tuition/JC Biology Tutor

    …continued.

    28. In an investigation to determine the effect of temperature on the activity of an enzyme, the time for all the substrate to disappear from a standard solution was recorded. Which graph shows the results of this investigation?

    The answer is C, a curve the shape of a smiley, with time at the y-axis and temperature on the x-axis. Remember that the temperature affects the rate of an enzyme catalysed reaction by a curve which has two parts – an exponentially increasing front portion and a steeply declining back portion? Refer to your notes on page 16. When the temperature is very low the reaction rate is very low, hence reaction time/duration is very long, thats why higher on the y-axis. As the temperature increases there is an exponential increase in reaction rate (page 16), therefore there is an exponential decrease in reaction duration (graph C). And there is this optimum temperature where the reaction rate is highest (page 16), which is when the reaction duration is shortest (graph C). Beyond that temperature, increasing temperature further causes denaturation of the enzyme hence a steep decline in the reaction rate (page 16) that is why there is a steep increase in reaction time (graph C). See the correlation between rate and duration? The graph on page 16 of your notes is actually like the graph in option C, hope you saw the link in their gradients!

    30. Which graph shows the effect of increasing enzyme concentration on product formation when there is an excess of substrate?

    The answer is B, increase and then plateaus off. When there is an excess of substrate, the question implies that substrate is NOT a limiting factor. The limiting factor is therefore the enzyme concentration. (Note the synergistic relationship between substrate and enzyme, when one is limiting the other is definitely not-limiting and in excess. Analogy: gender ratio in the world population. If there is limiting number of males then the number of females is definitely in excess of the males and thus non-limiting). Back to the question. So if enzyme concentration is a limiting factor, increasing enzyme concentration would have an effect on the concentration of the product. Therefore we see changes in all four curvess. Enzyme concentration increase would increase product concentration but take note that it must plateau off because when enzyme concentration is so high that it is no longer a limiting factor, then substrate concentration would be. If you have just this amount of substrates in your reaction, no matter how much enzymes you add it will ultimately only form this amount of products. Hence the plateau.

    31. The diagram shows how the enzyme glutamine synthetase removes the ammonia produced during plant metabolism.
    Ammonia + glutamate —glutamine synthetase—> glutamine

    Some herbicides contain an active agent which resembles glutamate. What is the likely mode of action of this agent?

    A it acts as an end product inhibitor
    B it acts as a competitive inhibitor
    C it decreases levels of ammonia
    D it increases levels of glutamate

    The answer is B, competitive inhibitor. This is because the herbicide bears structural resemblance to glutamate which is the substrate. Therefore the herbicide agent would compete with the substrate for the active site. Hence most likely it would act as a competitive inhibitor. It cannot be an end product inhibitor because glutamate is not an end product, glutamate is the substrate. Bearing resemblance to glutamate must involve some substrate-inhibitor competition.

    34. A medical scientise investigates four species of insects. He knows that one feeds on human blood and that the others feed on plants. As the insects look similar, he investigates the digestive enzymes present in their guts. Y indicates presence, N indicates absence. Which insect feeds only on blood?

    Insect A is amylase Y lipase N protease Y sucrase Y
    Insect B is amylase Y lipase N protease N sucrase Y
    Insect C is amylase N lipase Y protease Y sucrase Y
    Insect D is amylase N lipase Y protease N sucrase N

    The answer is Insect A. Hemoglobin in red blood cells are often digested by these insects, and hemoglobin is a protein. Definitely the blood sucking bugs need proteases, which digest proteins. Weak concentrations of sucrase and amylase have been found to be present in their guts too. But they lack lipases because lipid and fat digestion is not needed/relevant. In contrast, plant feeding insects would need a bit of everything.

    37.The diagram shows the structure of a competitive inhibitor of the enzyme lysozyme. Which substance is most likely to be the normal substrate of lysozyme?

    A lipid
    B polynucleotide
    C polypeptide
    D polysaccharide

    The answer is D, polysaccharide. The answer is not B, please take note of the error! Does this solve your doubts? The normal substrate should bear resemblance to the competitive inhibitor of lysozyme. Hence it should look like the structure given. And that structure actually looks like a beta-glucose polymer. Hence the answer is polysaccharide.

    Hope this helps!
    Ms Goh

    Diana Goh
    Participant

    A-Level Biology Tuition Singapore/H2 Biology Tuition/JC Biology Tutor

    Here are the requested explanations to the questions in the Enzyme Speed Test, for JC1 class.

    4. Which one of the following enzymes has the greatest substrate specificity?
    A lipase
    B nuclease
    C pepsin
    D sucrase
    E trypsin

    The answer is E, trypsin. A lipase is a name given to any enzyme that digests fats and lipids. A nuclease is a name given to any enzyme that acts on nucleic acids. A sucrase is a name given to any enzyme which can digest sucrose to its monomers glucose and fructose. Pepsin is slightly more specific, it digests proteins but it’s quite specific in that it cleaves peptide bonds between hydrophobic and aromatic amino acids. Trypsin is most specific because it specifically digests proteins only at the carboxyl side of lysine and arginine, when either of which is followed by a proline residue.

    7. Which one of the following bonds permanently to the active site of an enzyme?
    A allosteric inhibitor
    B coenzyme
    C competitive inhibitor
    D non-competitive inhibitor
    E substrate

    The answer is D, noncompetitive inhibitor. Remember I mentioned that noncompetitive inhibitors bind allosteric sites? Here is an exception. Sometimes, like in this case, the question wants the best answer from you. Look at the list of choices, they are all impossible except for D. A binds allosteric site for sure, that’s why the name. B does not bind permanently, read up coenzymes in the notes given. C binds the active site for sure but definitely not permanent, that’s why known as competitive. E definitely not permanent too, if not there would be no product! So this is a tricky question. Non competitive inhibitors may bind active sites permanently, it is a form of Irreversible inhibition. It clogs up the active site.

    14. The reaction rate of salivary amylase on starch decreases as the concentration of chloride ions is reduced. Which of the following describes the role of the chloride ions?
    A allosteric inhibitors
    B coenzymes
    C cofactors
    D competitive inhibitors
    E noncompetitive inhibitors

    The answer is C, cofactors. Refer to your notes on page 22, last sentence at the bottom. The exact same example is there. There are three types of cofactors – inorganic ions, prosthetic groups and coenzymes. Chloride Ion is an Inorganic Ion Cofactor.

    16.Fructose syrup is used as a sweetener in the food industry and the scheme below outlines the major steps in its industrial production from starch. The process makes use of bacterial or fungal enzymes at steps 1,2 and 3. The three arrows are in chronological order, first one involves enzyme 1, second arrow enzyme 2 and third enzyme 3.

    Starch suspension –> Maltose –> Glucose –> Fructose syrup in water
    In the table below, Y means the step could be carried out by heating the subtrate with acid as an alternative to using enzymes. N means that it could not. Which is the correct combination?
    1 2 3
    A Y N Y
    B Y Y N
    C N Y Y
    D N N N

    The answer is B, YYN. This is because the treatment of heat with acid is actually stimulating the process of hydrolysis. Hydrolysis is the breakdown of a molecule into two parts by the addition of a water molecule. Enzyme 3 cannot be replaced by acid because in that reaction you are not catalyzing the breakdown of a substrate. You are catalyzing the CONVERSION of glucose to fructose. Something interesting here, Fructose is C6H12O6, same as glucose! Same but different, and the difference lies in that Glucose has an aldehyde group and Fructose has a Ketone group. The two are actually isomers of each other. Therefore, the conversion of glucose to fructose is an isomerism process and the enzyme involved is called glucose isomerase.

    26.The diagram shows the initial rate of reaction using constant amounts of substrate and enzyme at different temperatures. X labels the part which is decreasing. What is the reason for the decline in the level of activity in region X, when temperature is very high?

    A breaking of sulfur bridges and ionic bonds in the enzyme
    B competition between substrate and product for the active site
    C hydrolysis of peptide bonds and breaking of hydrogen bonds in the enzyme
    D insufficient substrate to occupy all the active sites

    The answer is A, breaking of sulfur bridges and ionic bonds in the enzyme. B is impossible, it has nothing to do with substrate product competition. D is impossible because temperature rise does not reduce substrate availability. C is right in the second part, hydrogen bonds break at high temperatures, disrupting the secondary and tertiary structures. However, the first part is wrong because heat does not break peptide bonds. The primary structure remains INTACT with enzyme denaturation, only secondary tertiary and quaternary structures are affected. A is right because if the temperature is high enough even strong covalent bonds like sulfur bridges and ionic bonds may be broken.

    Diana Goh
    Participant

    A-Level Biology Tuition Singapore/H2/H1 Biology Tuition/JC Biology Tutor

    J1 Class 9-11am 1/5/12

    Today we finished up the chapter on Cellular Functions! We have embarked on the first assignment of the cellular functions chapter. Here’s a review to all that we have learned!
    http://www.cellsalive.com/cells/cell_model.htm

    J2 Class 11-1pm 1/5/12

    For today’s class we went through last week’s class test on Cell Signaling. Take note of the answering techniques you’ve learned. Remember, the Theory of Dissection! You know and I know what it means. πŸ™‚ Apply this to all the questions and concepts you learn, and you will find that you are actually blessed with an amazing depth and breadth of molecular details for even the simplest mechanism. For instance, describe the structure of the beta adrenergic receptor [3].
    The answer is based on the three domains of the receptor protein, recall them!

    Here is a video for Epinephrine GPCR signaling pathway and the steroid hormone receptor pathway. The difference is that the former is a membrane receptor and the latter is an intracellular receptor. Why this distinction? Think about the difference between Epinephrine and Steroids. πŸ™‚
    http://highered.mcgraw-hill.com/olc/dl/120109/bio48.swf
    http://highered.mcgraw-hill.com/olc/dl/120109/bio46.swf

    J1 Class 1-3pm 1/5/12

    The second part of the biology marathon, we had a lecture on Enzymes today. We discussed about Enzymes, the protein molecules which orchestrate the multitude of biochemical processes in our system! Here is an enzyme of how sucrase catalyses the breakdown of sucrose, an example of an enzyme mediated reaction to better your understanding.
    http://highered.mcgraw-hill.com/sites/0072507470/student_view0/chapter25/animation__enzyme_action_and_the_hydrolysis_of_sucrose.html

    Cheers,
    Ms Diana Goh

    • This reply was modified 13 years, 10 months ago by Diana Goh.
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    Diana Goh
    Participant

    A-Level Biology Tuition Singapore/H2/H1 Biology Tuition/JC Biology Tutor

    J1 Class 23/04/2012

    Today, we wrapped up the first part of the chapter on Cellular Functions (The Plasma Membrane). Covered some of the answering techniques required to tackle questions in this chapter.

    We also started on the second part of the Cellular Functions chapter (The Cellular Organelles) – looking at the largest and smallest organelles in the cell – Nucleus and Ribosomes. Next week we would finish up the rest of the organelles in the cell. Read up chapter 6 of Campbell as well as the notes given before lesson begins next week!

    An interesting topic of discussion fueled today’s lesson, the Endosymbiotic Theory, otherwise known as the Theory of Endosymbiosis. Do read up a little on it online and in your textbook.. and I shall tell you more next week!

    Ms Diana Goh

    Diana Goh
    Participant

    A-Level Biology Tuition Singapore/H2/H1 Biology Tuition/JC Biology Tutor

    J2 Class 22/04/2012

    Cell Signaling class test 1hour 15mins. Answers will be given next lesson.

    Having understood the molecular mechanisms of cell signaling and communication (how cells talk to each other), we are now moving on to a more macro chapter, where we look at the concepts of cell-communication can be applied to bigger systems (the endocrine and the nervous control), and how our body regulates homeostasis (a constant internal environment).

    Do read up on Endocrine control, chapter 45 of Campbell and Reece, and be prepared for a lecture next Saturday!

    In Endocrine control we focus on the regulation of blood glucose levels. Here’s a snippet of what we will be learning next week!

    http://outreach.mcb.harvard.edu/animations/homeostasis10.swf

    Cheers,
    Ms Diana Goh

    Diana Goh
    Participant

    A-Level Biology Tuition Singapore/H2/H1 Biology Tuition/JC Biology Tutor

    J1 Class 21/04/2012
    Check out the structure of hemoglobin in 3D! Have fun learning πŸ™‚
    Do note that you’re supposed to know about Sickle Cell Disease and how it is due to changes in the structure of Hemoglobin.

    Hemoglobin and Sickle hemoglobin structure
    http://www.umass.edu/molvis/tutorials/hemoglobin/index.htm

    Sickle cell disease
    http://www.youtube.com/watch?v=R4-c3hUhhyc&feature=related

    Cheers,
    Ms Diana Goh

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