STUDI PENGARUH PENAMBAHAN GLISEROL DAN SORBITOL TERHADAP STABILITAS ENZIM SELULASE DARI Bacillus subtilis ITBCCB148

0817011059, Sundari Riawati (2012) STUDI PENGARUH PENAMBAHAN GLISEROL DAN SORBITOL TERHADAP STABILITAS ENZIM SELULASE DARI Bacillus subtilis ITBCCB148. Digital Library.

[img]
Preview
File PDF
ABSTRAK.pdf

Download (16Kb) | Preview
[img]
Preview
File PDF
BAB I.pdf

Download (20Kb) | Preview
[img]
Preview
File PDF
BAB II.pdf

Download (160Kb) | Preview
[img]
Preview
File PDF
BAB III.pdf

Download (45Kb) | Preview
[img] File PDF
BAB IV.pdf
Restricted to Hanya pengguna terdaftar

Download (336Kb)
[img]
Preview
File PDF
BAB V.pdf

Download (16Kb) | Preview
[img]
Preview
File PDF
Cover.pdf

Download (15Kb) | Preview
[img]
Preview
File PDF
curiculum vitae.pdf

Download (140Kb) | Preview
[img]
Preview
File PDF
Kata Mutiara.pdf

Download (33Kb) | Preview
[img]
Preview
File PDF
Lembar Pengesahan.pdf

Download (28Kb) | Preview
[img]
Preview
File PDF
Persembahan.pdf

Download (20Kb) | Preview
[img]
Preview
File PDF
Riwayat hidup.pdf

Download (19Kb) | Preview
[img]
Preview
File PDF
Sanwacana.pdf

Download (15Kb) | Preview

Abstrak (Berisi Bastraknya saja, Judul dan Nama Tidak Boleh di Masukan)

Abstrak Penelitian ini bertujuan untuk mempelajari pengaruh penambahan gliserol dan sorbitol terhadap stabilitas enzim selulase dari Bacillus subtilis ITBCCB148. Untuk mencapai tujuan tersebut dilakukan produksi, isolasi, dan pemurnian enzim. Pemurnian enzim selulase dilakukan dengan menggunakan kromatografi kolom filtrasi gel Sephadex G-100. Enzim hasil pemurnian kemudian ditambahkan gliserol dan sorbitol. Penentuan aktivitas enzim selulase dilakukan dengan metode Mandels sedangkan pengukuran kadar protein dilakukan dengan metode Lowry. Hasil penelitian menunjukkan bahwa enzim hasil pemurnian memiliki aktivitas spesifik sebesar 4,6458 U/mg, meningkat 4,93 kali dibandingkan ekstrak kasar enzim dengan perolehan 12,60%. Enzim ini memiliki pH optimum 5,5; suhu optimum 50oC; ki = 0,0121 menit-1 ; t1/2 = 57,27 menit; dan ∆Gi = 102,19 kJ mol-1. Enzim setelah penambahan gliserol 0,5; 1,0; dan 1,5 M memiliki pH optimum dan suhu optimum yang sama dengan enzim hasil pemurnian. Uji stabilitas termal enzim setelah penambahan gliserol 0,5 M pada suhu 50oC selama 100 menit memiliki t1/2 = 72,19 menit, ki = 0,0096 menit-1 dan ∆Gi = 102,82 kJ mol-1; gliserol 1,0 M memiliki t1/2 = 82,50 menit, ki = 0,0084 menit-1 dan ∆Gi = 103,17 kJ mol-1; dan gliserol 1,5 M memiliki t1/2 = 80,58 menit, ki = 0,0086 menit-1 dan ∆Gi = 103,11 kJ mol-1. Enzim setelah penambahan sorbitol 0,5; 1,0; dan 1,5 M memiliki pH optimum dan suhu optimum yang sama dengan enzim hasil pemurnian. Uji stabilitas termal enzim setelah penambahan sorbitol 0,5 M pada suhu 50oC selama 100 menit memiliki t1/2 = 90,00 menit, ki = 0,0077 menit-1 dan ∆Gi = 103,41 kJ mol-1; sorbitol 1,0 M memiliki t1/2 = 99,00 menit, ki = 0,0070 menit-1 dan ∆Gi = 103,66 kJ mol-1; dan sorbitol 1,5 M memiliki t1/2 = 92,40 menit, ki = 0,0075 menit-1 dan ∆Gi = 103,48 kJ mol-1. Walaupun suhu optimum dan pH optimum enzim setelah penambahan gliserol dan sorbitol tidak mengalami perubahan, tetapi terjadi peningkatan stabilitas termal karena adanya penurunan nilai ki serta peningkatan waktu paruh dan ∆Gi. Kata Kunci: Enzim selulase, gliserol, sorbitol, Bacillus subtilis ITBCCB148 Abstract This research aims to study the effect of addition glycerol and sorbitol toward stability cellulase enzyme from Bacilus subtilis ITBCCB148. To approach this aims, the production, isolation and purification of the enzyme were done. The purification of cellulase enzyme was done by using gel filtration chromatography column of Sephadex G-100. The pure enzyme is added by glycerol and sorbitol. Determination of cellulase enzyme activity performed by the method of Mandels while the measurement of protein levels performed by the method of Lowry. The results showed that the pure enzyme has specific activity 4,6458 U/mg, the pureness increase 4,93 times than native enzyme with the result 12,60%. This enzyme has optimum pH 5,5; optimum temperature 50°C; ki = 0,0121 min-1; t1/2 = 57,27 min; and ΔGi = 102,19 kJ mol-1. Enzyme after addition glycerol 0,5; 1,0; and 1,5 M have optimum pH and temperature same with pure enzyme. The test of thermal stability of the enzyme after addition glycerol 0,5 M at temperature 50°C for 100 min has t1/2 = 72,19 min, ki = 0,0096 min-1 and ΔGi = 102,82 kJ mol-1; glycerol 1,0 M has t1 /2 = 82,50 min, ki = 0,0084 min-1 and ΔGi = 103,17 kJ mol-1; and glycerol 1,5 M has t1/2 = 80,58 min, ki = 0,0086 min-1 and ΔGi = 103,11 kJ mol-1. Enzyme after addition sorbitol 0,5; 1,0; and 1,5 M have optimum pH and temperature same with pure enzyme. The test of thermal stability of the enzyme after addition sorbitol 0,5 M at temperature 50°C for 100 min has t1/2 = 90,00 min, ki = 0,0077 min-1 and ΔGi = 103,41 kJ mol-1; sorbitol 1,0 M has t1/2 = 99,00 min, ki = 0,0070 min-1 and ΔGi = 103,66 kJ mol-1, and sorbitol 1,5 M has t1/2 = 92,40 min, ki = 0,0075 min-1 and ΔGi = 103,48 kJ mol-1. Although the optimum pH and temperature of the enzyme after addition glycerol and sorbitol have not changed, but an increase in thermal stability due to a decrease in the value of ki as well as increase half life and ΔGi. Key word: Cellulase enzyme, glycerol, sorbitol, Bacillus subtilis ITBCCB148

Jenis Karya Akhir: Artikel
Subyek:
Program Studi: FAKULTAS MIPA > Prodi Kimia
Pengguna Deposit: IC-STAR . 2015
Date Deposited: 22 Oct 2015 08:57
Terakhir diubah: 22 Oct 2015 08:57
URI: http://digilib.unila.ac.id/id/eprint/13589

Actions (login required)

Lihat Karya Akhir Lihat Karya Akhir