OPTIMIZATION OF CHITOSAN HYDROLYSIS BY RECOMBINANT CHITOSANASE FROM BACILLUS AMYLOLIUEFACIENS ABBD FOR ANTIBACTERIAL SCREENING
Indonesia is an archipelago country that has abundant fishery resources. One of them is a <br /> <br /> group of crustaceans such as shrimp and crab. Based on statistical data from the Ministry <br /> <br /> of Marine Affairs and Fisheries of Indonesia, production of shrimp i...
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Format: | Final Project |
Language: | Indonesia |
Online Access: | https://digilib.itb.ac.id/gdl/view/28682 |
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Institution: | Institut Teknologi Bandung |
Language: | Indonesia |
Summary: | Indonesia is an archipelago country that has abundant fishery resources. One of them is a <br />
<br />
group of crustaceans such as shrimp and crab. Based on statistical data from the Ministry <br />
<br />
of Marine Affairs and Fisheries of Indonesia, production of shrimp in Indonesia has <br />
<br />
reached 645,000 tons/year and with 56,200 tons/year waste. The wastes of shrimp shell <br />
<br />
contain of 17–20% chitin. Chitosan (derived from deacetylation of chitin) can be utilized <br />
<br />
to be a high-value material for industrial purposes. Hydrolysis of β-1,4-glycosidic bond of <br />
<br />
chitosan using chitosanase (EC 3.2.1.132) produces chitooligosaccharides. This <br />
<br />
compound has many advantages for industrial use such as water-soluble and has various <br />
<br />
bioactivity including antibacterial, antifungal, anti-inflammatory, and antidiabetic. The <br />
<br />
aims of this study are to produce and purify recombinant chitosanase (rek-Csn) from <br />
<br />
marine bacteria Bacillus amyloliquefaciens ABBD on Escherichia coli BL21 (DE3), and <br />
<br />
to analyze hydrolysis chitosan by rec-Csn product. Cell that contain rec-Csn were cultured <br />
<br />
in Lysogeny Broth media with the addition of isopropyl β-D-1-thiogalactopyranoside <br />
<br />
(IPTG) after the cell reached a degree of turbidity (OD600) a number of 0.6–0.8. Cultured <br />
<br />
cells were incubated 37 °C for 4 hours. Cell pellets are then lyzed and the supernatant is <br />
<br />
purified by cation exchange chromatography (CM TOYOPEARL). The analysis result of <br />
<br />
Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis (SDS-PAGE) showed the <br />
<br />
rec-Csn that protein produced was pure and had a molecular mass of ~27 kDa. The rec- <br />
<br />
Csn protein has a specific activity of 1594,86 U/mg at pH 6 and a temperature of 50 °C. <br />
<br />
The product of chitosan hydrolysis by rec-Csn produces chitooligosaccharides which has <br />
<br />
antibacterial bioactivity. |
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