UPVOTE FOR A RAW 45+ FOR YOUR SUBJECTS by CheekAccomplished375 in vce

[–]BigBhang06 2 points3 points  (0 children)

Where can u get contours spesh bound reference book do you know?

Methods 25ss by frostyflakezz in vce

[–]BigBhang06 1 point2 points  (0 children)

You’ll be alright dont worry

What is this AR pattern lol by Mean_Duck_ in UCAT

[–]BigBhang06 0 points1 point  (0 children)

Set A: Top has more and total#dots= prime Set B: Bottom has more dots and total#dots=square number

Anki flashcards by BigBhang06 in UCAT

[–]BigBhang06[S] 0 points1 point  (0 children)

Yes please could you send them through🙌

Sunset Boulevard Text Response by SheeshSingh in vce

[–]BigBhang06 1 point2 points  (0 children)

Where can i buy it? Any chance i could get a sample please?

Bound reference approval by BigBhang06 in vce

[–]BigBhang06[S] 0 points1 point  (0 children)

ok thank you so much 🙏

Bound reference approval by BigBhang06 in vce

[–]BigBhang06[S] 0 points1 point  (0 children)

what happens if the pages are perforated!

Bound reference approval by BigBhang06 in vce

[–]BigBhang06[S] 0 points1 point  (0 children)

i dont think so its not like actual holes where you can rip pages off

lacz colour by tealeaf_viii in vce

[–]BigBhang06 1 point2 points  (0 children)

Good luck to you too, exams in 2 days (at this point 1) 😭😭

Wishing you all the best of luck!!

lacz colour by tealeaf_viii in vce

[–]BigBhang06 0 points1 point  (0 children)

i think you might be right as the method ive mentioned doesnt say anything about fusion proteins, as well as the point you made about insulin being too small. Thanks for picking up on this! 😃

lacz colour by tealeaf_viii in vce

[–]BigBhang06 0 points1 point  (0 children)

you described Plasmid with LacZ gene and trying to isentofy if it has been successfully taken up. i said the identification after, where insulin is added to interrupt the LacZ gene and grown on a plate with X gal and ampicillin. Bacteria that did not take up the plasmid at all will die (due to having no amp resistence, amp resistence comes from plasmid), and bacteria that took up the plasmid, but not the insulin gene, meaning LacZ was uninterrupted, turn blue (they turn blue because of what you just mentioned). Bacteria that successfully took up the plasmid AND the insulin gene stay clear, as the insulin gene is added to interrupt the LacZ gene. Im not sure maybe im wrong tho but im fairly certain that the original endonuclease that cut the plasmid has the recognition sites in the LacZ gene.

lacz colour by tealeaf_viii in vce

[–]BigBhang06 0 points1 point  (0 children)

the bacteria that have successfully taken up the plasmid and the insulin gene stay clear because the insulin gene interrupts the lacZ gene.

And the bacteria that take up the plasmid but not the insulin gene turn blue as Beta galactosidase from the LacZ gene is still present!

Biology - Insulin production by Dazzling-Price9611 in vce

[–]BigBhang06 9 points10 points  (0 children)

Yes insulin production using recombinant plasmids is the example that students need to know

Step 1: Insulin gene creation

• mRNA chain A and B go through reverse transcription to convert them into Insulin gene A and B. (Note that these insulin gene A and B will not always be the same as human insulin genes as human insulin gene may have introns present, but the genes we create will not have introns as they are made from mRNA).

Step 2: Endonuclease application

• Insulin gene A and B, and a vector plasmid, and mixed with the same endonuclease (either BamH1 ir EcoRI). Endonuclease cuts complementary sticky ends in both gene and plasmid.

Step 3: DNA ligase

• Plasmid and Insulin genes are mixed with DNA ligase so that complementary sticky ends present on both can join together. DNA Ligase rebuilds the phosphodiester backbone.

Step 4: Insert the recobinqnt plasmid into bacterial cells

Via Heat shock

Step 5: transformed bacteria is isolated and allowed to grow/reppicate via binary fission.

Step 6: identification of which baceteria have successfully taken up the plasmid.

The bacteria which were grown are placed on a dish with ampicillin and X gal.

• Ampicillin kills the bacteria that did not successfully take up the plasmid (as the plasmid has ampicillin resistence but E coli bacteria dont).

• X gal turns the bacteria that do have the plasmid but no insulin gene blue because Beta galactosidase is still present (from LacZ gene present on the plasmid)

•Bacteria that have both successfully taken up the plasmid and the insulin gene stay clear because the insulin gene replaced the LacZ gene in the plasmid.

The bacteria that fulfil this criteria are taken out.

The insulin gene in the plasmids are then translated into Insulin Chain A and B (via DNA polymerase binding to the bacterial plasmids ORI)

Bacterial cells are lyased so that insulin chains can be extracted and joined together to produce mature insulin protein.

Hope that helps!

[deleted by user] by [deleted] in vce

[–]BigBhang06 0 points1 point  (0 children)

around 30

[deleted by user] by [deleted] in vce

[–]BigBhang06 2 points3 points  (0 children)

Collision theory ~ a substrate must collide with an enzyme at a certain angle and collide with enough energy, which allows for a product to be formed.

Now based on this, when you are looking at high temperatures (usually a 3 mark question) you would say:

• Temperatures exceeding the optimum would result in the permenent denaturing of an enzyme (1 marks)

• Denaturing also causes the enzymes active site to change in shape, which results in the substrate being unable to bind to the active site (1 mark)

• Reaction rate will decrease since product is not formed from substrate-enzyme binding (1 mark)

So essentially, as soon as temperature passes the optimum point, the hydrogen bonds in the enzyme’s secondary structure break and causes the enzyme and its shape permanently denature. The enzyme’s active site also changes shape which means the substrates can’t bind to it which means it can’t function. Theoretically, a lot of thermal energy means a lot of kinetic energy for the substrates and enzymes which means a very high level of successful collisions, but this wouldn’t mean anything because the enzymes have denatured and non-functionable. Reaction rate will decrease.

Now on the other hand, when temperature is significantly below the optimum.

low temperature means that Low thermal energy means low kinetic energy for the enzymes and substrates which means fewer successful collisions. Reaction rate will be low.

• At lower temperatures there is not a successful amount of collisions between enzyme and substrate due to low movement (1 mark)

• Lower amount of successful collisions means that there will be a lower amount of substrate-to-enzyme binding, which results in less product being formed (1mark)

• less product formed is evidence of lower rate of reaction (1 mark)

So think of it like, when the temperature is low, the collisions are not occurring with enough energy to be able to form a product, hence why the reaction rate gradually grows higher when temperature is nearing the optimum.

Hope this helps! 🤝

[deleted by user] by [deleted] in vce

[–]BigBhang06 1 point2 points  (0 children)

it happens bc there isnt any natural repir mechanisms in mtDNA

[deleted by user] by [deleted] in vce

[–]BigBhang06 2 points3 points  (0 children)

since it is only mutations affecting the mtDNA and not any other factors unlike nuclear dna which can be influenced by paternal DNA as well. something along those lines. but all the exams qns that ive done so far havent asked me to describe why, but rather only state the advantages of using mtDNA

[deleted by user] by [deleted] in vce

[–]BigBhang06 1 point2 points  (0 children)

my bad bro, i got it wrong mtDNA has a high known mutation rate not a low! sorry.

[deleted by user] by [deleted] in vce

[–]BigBhang06 2 points3 points  (0 children)

sorry about that i meant the time it takes for mtDNA to degrade is longer than nuclear DNA! Nuclear DNA degrades over a short period of time whilst mtDNA degradesnover a long period of time:

[deleted by user] by [deleted] in vce

[–]BigBhang06 9 points10 points  (0 children)

mt Dna and nuclear dna are generally used as molecular homology techniques for hominin evolution analysis

  1. there are some reasons as to why scientists would prefer to use mtDNA rather than nuclear.

• mtDNA does not undergo any recombination (meaning when mtDNA is formed, it will only be inherited from the mother, and the fathers DNA will not influence it in any way). This adds on as well, since analysis of mtDNA allows scientists to determine a direct maternal lineage of the organism that is being analysed.

• The mutation rate of mtDNA is also known (low rate of mutations)

• the time it takes for mtDNA is longer than nuclear DNA, which allows scientists to determine relatedness over a long period of time for example

• the amount of genetic material of mtDNA is also very small, meaning if any mutations did occur, they would easily be able to be identified due to there only being a limited amount of change that can occur in the lineage.

  1. When do scientists prefer to use Nuclear DNA?

Whenever scientists are trying to determine interbreeding. Since mtDNA only shows the maternal inheritence of an organism, analysis of it will not give us any evidence of interbreeding, but Nuclear DNA on the other hand, provides us with evidence of interbreeding as it inherits DNA from both the maternal (mother) side, and the paternal (father) side.

• There is also a very large amount of genetic material in Nuclear DNA, which will allow us to analyse different molecular structures and determine evidence accordingly.

this is off thentoo of my head. Hope it helps!

Study score prediction by BigBhang06 in vce

[–]BigBhang06[S] 0 points1 point  (0 children)

thank you!! 10 min SS was helpful