You need to login first

Login information

Haven't yet registered?

×
* * * *

Donate

If you found our community helpful, your small donation will continue to help us reach more students around the globe.
PayPal
Pages: 1     Go Down
  New Topic  |  Print  
How does salt affect catalase breaking down hydrogen peroxide
Read 10911 times | 17 Replies | Average Rating: Not Rated Yet
buddah
Octopus
**
Posts: 45
Points: 380
Rep:  +1   -0


For a more comfortable homework help experience, try HomeworkClinic.com.
How does salt affect catalase breaking down hydrogen peroxide

Report this PostReport Abuse
Reply# 1
*
Posts: 12117
Points: 4257
Rep:  +704   -2

4 years ago

A heavy salt concentration would likely interact with the amino acids making up the catalase protein, thereby preventing its catalytic site from converting H2O2 into water and oxygen. Recall that NaCl breaks down into it's ionic form Na+ and Cl-. Any negative side-group would interact with the positive sodium ion.



Report this PostReport Abuse
 
Reply# 2
Posts: 45
Points: 380
Rep:  +1   -0

4 years ago

thanks, we used 3% and 10 % of both Lead (II) Nitrate and Copper (II) Sulphate, but im confused because when we did the actual lab lead nitrate no oxygen was released by the lead nitrate. does this mean it cant break down the hydrogen peroxide or doesnt mean it didnt denature the catalase? Undecided Undecided



Report this PostReport Abuse
Reply# 3
*
Posts: 12117
Points: 4257
Rep:  +704   -2

4 years ago

A sulphate will likely interact with amino acids in the catalytic site. It wouldn't denature the catalase, it would just inhibit it. In fact, copper (II) sulphate is an irreversible, non-competitive inhibitor of catalase - so it likely inhibits it at an allosteric site on the enzyme. Recall, enzyme inhibitors decrease the activity of an enzyme. The better the inhibitor is, the greater the decrease in the catalysis. The rate of the decomposition reaction will decrease when it is added to the reaction mixture. I would also assume that the heavy metal, lead (pb) would also inhibit the enzyme, though I'm not too sure how.



Last Edit: 4 years ago by bio_man Report this PostReport Abuse
 
Reply# 4
*
Posts: 7839
Points: 4043
Rep:  +345   -10

4 years ago

Smile Attachment



Attached file(s)* Lead_and_Mercury.pdf (70.86 KB - downloaded 9 times.)
Report this PostReport Abuse
 
Reply# 5
Posts: 45
Points: 380
Rep:  +1   -0

4 years ago

omg i swear man you guys deserve an award or something youre soo F**** helpful man!!!!! damnnnn, i have to donate to this site. THANK YOU SO MUCH. not only am i learning better am also understanding better awesome work guys thanks.

p.s i may still have more questions Too Funny



Report this PostReport Abuse
Reply# 6
*
Posts: 12117
Points: 4257
Rep:  +704   -2

4 years ago

omg i swear man you guys deserve an award or something youre soo F**** helpful man!!!!! damnnnn, i have to donate to this site. THANK YOU SO MUCH. not only am i learning better am also understanding better awesome work guys thanks.

p.s i may still have more questions Too Funny

Yep, keep them coming.



Report this PostReport Abuse
 
Reply# 7
Posts: 45
Points: 380
Rep:  +1   -0

4 years ago

alright heres my introduction, please take a look at it and tell me what i can add or remove to making it really good, i need to do really well on this lab. I have attached it



Attached file(s)* Catalase Lab - Dunmola.docx (12.51 KB - downloaded 5 times.)
Report this PostReport Abuse
Reply# 8
Posts: 45
Points: 380
Rep:  +1   -0

4 years ago

Disregard the attachment above, that just consists of the introduction. Here is the one have been working on, it consists of the intro, hypothesis and purpose. Please take a look at it and help me thanks.



Attached file(s)* Catalase Lab - Dunmola.docx (14.45 KB - downloaded 10 times.)
Report this PostReport Abuse
Reply# 9
*
Posts: 7839
Points: 4043
Rep:  +345   -10

4 years ago

Disregard the attachment above, that just consists of the introduction. Here is the one have been working on, it consists of the intro, hypothesis and purpose. Please take a look at it and help me thanks.

buddah could you post it on here, like the part you need us to edit?



Report this PostReport Abuse
 
Reply# 10
Posts: 45
Points: 380
Rep:  +1   -0

4 years ago

is there another way, i can show you, just because i dont want it on the web, because i have to submit to turn it in and i dont want it 2 come up here



Report this PostReport Abuse
Reply# 11
*
Posts: 7839
Points: 4043
Rep:  +345   -10

4 years ago

It won't get far if you post a section on here. I don't do side jobs for free Undecided



Report this PostReport Abuse
 
Reply# 12
Posts: 45
Points: 380
Rep:  +1   -0

4 years ago

Hypothesis

Part a – Catalase Concentration
If there is an excess in hydrogen peroxide and the concentration of catalase is increased, the rate of catalysis will also be increased; however, if there’s a shortage of hydrogen peroxide, the increase of catalase concentration will have no effect in the reaction; Therefore, the activity of catalase under greater concentrations of it, is dependent on the amount of hydrogen peroxide there is. This will be the case because when there is an excess of hydrogen peroxide and excess catalase concentration there will be more substrate binding in the active sites; however, if there is more hydrogen peroxide than catalase concentration, then the reaction will not occur any faster because hydrogen peroxide would have taken up all the active sites and there would be a bunch of hydrogen peroxide molecules doing nothing. If there is more catalase concentration then hydrogen peroxide then active sites would be left empty with no substrate to bind with, leading to a slower reaction time. To conclude, catalase concentration must be relative to hydrogen peroxide concentration for catalysis to increase.

Part b – Catalase activity under heavy metal ions
The activity of catalase under heavy metal ions: Copper (II) Sulphate and Lead (II) Nitrate will reduce the rate at which catalase breaks down hydrogen peroxide. Copper (II) Sulphate will interact with the amino acids in the catalase; however, it won’t denature the catalase, since, Copper (II) Sulphate is a consider a non-competitive inhibitor of catalase it would just attach itself to another site on in the catalase molecule causing it to change shape so that the hydrogen peroxide molecule can no longer bind to the active site. This will result in the decrease of the decomposition reaction between hydrogen peroxide and catalase.Likewise, Lead (II) Nitrate is also an inhibitor of catalase; therefore, it will decrease the rate of catalysis aswell.

Alright here it is tell meh if its okay



Last Edit: 4 years ago by buddah Report this PostReport Abuse
Reply# 13
*
Posts: 7839
Points: 4043
Rep:  +345   -10

4 years ago

Part a – Catalase Concentration
If there is an excess in hydrogen peroxide and the concentration of catalase is increased, the rate of catalysis will also be increased; however, if there’s a shortage of hydrogen peroxide, the increase of catalase concentration will have no effect in the reaction; Therefore, the activity of catalase under greater concentrations of it, is dependent on the amount of hydrogen peroxide there is. This will be the case because when there is an excess of hydrogen peroxide and excess catalase concentration there will be more substrate binding in the active sites; however, if there is more hydrogen peroxide than catalase concentration, then the reaction will not occur any faster because hydrogen peroxide would have taken up all the active sites and there would be a bunch of hydrogen peroxide molecules doing nothing. If there is more catalase concentration then hydrogen peroxide then active sites would be left empty with no substrate to bind with, leading to a slower reaction time. To conclude, catalase concentration must be relative to hydrogen peroxide concentration for catalysis to increase.

The red contextually does not make sense; the green is perfect

Part b – Catalase activity under heavy metal ions
The activity of catalase under heavy metal ions: Copper (II) Sulphate and Lead (II) Nitrate will reduce the rate at which catalase breaks down hydrogen peroxide. Copper (II) Sulphate will interact with the amino acids in the catalase; however, it won’t denature the catalase, since, Copper (II) Sulphate is a consider a non-competitive inhibitor of catalase it would just attach itself to another site on in the catalase molecule causing it to change shape so that the hydrogen peroxide molecule can no longer bind to the active site (THIS IS CALLED THE ALLOSTERIC SITE). This will result in the decrease of the decomposition reaction between hydrogen peroxide and catalase.Likewise, Lead (II) Nitrate is also an inhibitor of catalase; therefore, it will decrease the rate of catalysis aswell.

Well done.



Report this PostReport Abuse
 
Pages: 1     Go Up New Topic Print
 
Related Topics
Replies Author Last post
2
Replies
Cell Biology | Started by buddah | Views: 2650
Last post Last post by Itzmc
4 years ago
1
Reply
High School Level Biology | Started by kingumang | Views: 1644
Last post Last post by duddy
3 years ago
2
Replies
Biochemistry | Started by Kurmis | Views: 1840
Last post Last post by Kurmis
3 years ago
3
Replies
Annoying Rants | Started by ilikepie1234 | Views: 460
Last post Last post by rkbrookover
3 years ago
Note: This topic is currently locked from adding new posts. Only administrators and moderators can reply. If you'd like to contribute to this topic, start a new thread and make reference to this one. Otherwise, contact a moderator for more options.