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Production and Purification of Chitosan from Horseshoe Crab, Tachypleus<br />

gigas<br />

Nurlyana Yasmin Binti Noor Hisham<br />

Supervisor: Assoc. Prof. Dr. Ahmad Shamsudin Bin Ahmad<br />

Bachelor of Science (Marine Biology)<br />

School of Marine and Environmental Sciences<br />

Chitin was extracted from carapace of Tachypleus gigas using chemical technique<br />

which involving two steps known as demineralization using HCl to remove CaCO3 and<br />

deproteinization using NaOH to remove proteins from the crude sample. Three<br />

different concentrations of HCl were used; 0.25 M, 1.0 M and 2.0 M for<br />

demineralization. Then, the product was deproteinized with 1.0 M of NaOH. The chitin<br />

produced was further derived into chitosan by deacetylation process to remove acetyl<br />

groups using 11 M NaOH. The average content of the carapace of horseshoe crab<br />

were calculated. Different HCl concentrations resulting different content values.<br />

Highest CaCO3 removed (76.65 ± 2.23%) when the sample treated using 2.0 M HCl.<br />

In contrast, treatment using 0.25 M HCl removed the highest amount of proteins<br />

(43.00 ± 6.25%).The highest chitin and chitosan yielded (21.25 ± 0.34% and 16.26<br />

± 0.73% respectively) from the treatment of sample using 1.0 M HCl.<br />

1834 | UMT UNDERGRADUATE RESEARCH DAY 2018

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