dc.contributor.advisor | Trilaksani, Wini | |
dc.contributor.advisor | Nurjanah | |
dc.contributor.author | Prastyo, Deny Tri | |
dc.date.accessioned | 2021-02-22T00:47:15Z | |
dc.date.available | 2021-02-22T00:47:15Z | |
dc.date.issued | 2021 | |
dc.identifier.uri | http://repository.ipb.ac.id/handle/123456789/106045 | |
dc.description.abstract | Ikan nila (Oreochromis niloticus) merupakan salah satu jenis ikan budidaya
yang produksinya terus meningkat. Pengolahan ikan nila menjadi produk siap
konsumsi menyisakan hasil samping, diantaranya adalah bagian kulit. Kulit ikan
diketahui dapat dimanfaatkan sebagai sumber alternatif kolagen halal dan
hidrolisatnya memiliki aktivitas biologis yang berguna bagi kesehatan tubuh
sehingga mampu meningkatkan nilai fungsinya. Penelitian ini bertujuan untuk
mengembangkan potensi kulit ikan nila sebagai sediaan bioaktif hidrolisat kolagen
yang mempunyai aktivitas antioksidan dan inhibitor enzim pengubah angiotensin
(ACE).
Penelitian ini terbagi menjadi tiga tahapan utama, yakni optimasi fase
pretreatment kolagen, ekstraksi kolagen dan hidrolisis kolagen. Optimasi proses
pretreatment menggunakan larutan NaOH dengan lama waktu yang berbeda
berdasarkan kandungan protein terlarut dan asam amino pada larutan sampel.
Ekstraksi kolagen dilakukan dengan metode asam dan sifat kolagen yang diperoleh
dideterminasi meliputi berat molekul, gugus fungsi, suhu transisi, nilai zeta
potensial serta nilai rendemen. Optimasi proses hidrolisis kolagen menggunakan
enzim papain komersil untuk menghasilkan hidrolisat kolagen terbaik berdasarkan
beberapa parameter uji meliputi derajat hidrolisis, aktivitas penghambatan
angiotensin converting enzyme (ACE), dan aktivitas antioksidan secara in vitro.
Hasil penelitian menunjukkan bahwa kondisi pretreatment terbaik pada
proses ekstraksi kolagen kulit ikan nila yakni selama 12 jam pada konsentrasi
NaOH 0,1 N, karakteristik kolagen merupakan kolagen tipe I diindikasikan adanya
rantai α1 dan α2. Rerata nilai rendemen kolagen kulit ikan nila dan hidrolisatnya
berturut-turut 17,05% dan 15,17%. Waktu hidrolisis, konsentrasi enzim serta
interaksi antar kedua faktor tersebut berpengaruh secara signifikan (p < 0,05)
terhadap nilai derajat hidrolisis, aktivitas penghambatan ACE dan aktivitas
antioksidan hidrolisat kolagen kulit ikan nila. Hidrolisat kolagen kulit ikan nila
yang dihidrolisis selama 120 menit dengan pemberian konsentrasi enzim sebesar
8000 U memiliki rerata persentase derajat hidrolisis 33,94%, serta rerata persentase
penghambatan ACE tertinggi yakni 74,78%. Pada kombinasi perlakuan yang sama
hidrolisat kolagen kulit ikan nila memiliki rerata nilai IC50 terbaik yakni 93,32
µg/mL, termasuk pada kategori senyawa antioksidan kuat. Persentase derajat
hidrolisis memiliki korelasi terhadap aktivitas penghambatan ACE dan aktivitas
antioksidan, dengan nilai koefisien korelasi Pearson berturut-turut 0,8592 dan -
0,4069. | id |
dc.description.abstract | Tilapia (Oreochromis niloticus) is a type of farmed fish whose production
continues to increase. Processing of tilapia into ready-to-consume products leaves
some side products, including the skin. Fish skin is known to be used as an
alternative source of halal collagen and its hydrolyzate has biological activity that
is useful for body health so that it can increase its function value. This study aimed
to develop the potential of tilapia skin as a collagen hydrolyzate which had
antioxidant and angiotensin converting enzyme (ACE) inhibitor activity.
This research was divided into three main stages, including optimization of
the collagen pretreatment, collagen extraction and collagen hydrolysis.
Optimization of the pretreatment process using NaOH solution with different
lengths of time based on the dissolved protein and amino acid content in the sample
solution. Collagen extraction was carried out by the acid method and the properties
of collagen obtained were determined including molecular weight, functional
group, transition temperature, zeta potential value and yield value. Optimization of
the collagen hydrolysis process using commercial papain enzymes to produce the
best collagen hydrolyzates based on several test parameters including the degree of
hydrolysis, inhibitory activity of angiotensin converting enzyme (ACE), and
antioxidant activity in vitro.
The results showed that the best pretreatment conditions in the collagen
extraction process was for 12 hours at a concentration of 0.1 N NaOH. The
characteristics of collagen were type I collagen which indicated α1 and α2 chains.
The average yield of tilapia skin collagen and its hydrolyzate were 17.05% and
15.17%, respectively. Hydrolysis time, enzyme concentration and the interaction
between the two factors had a significant effect (p<0.05) on the degree of
hydrolysis, ACE inhibitory activity and antioxidant activity of collagen
hydrolysate. Collagen hydrolyzed for 120 minutes with an enzyme concentration
of 8000 U had a percentage of degree of hydrolysis 33.94%, and the highest mean
percentage of ACE inhibition was 74.78%. In the same treatment combination,
tilapia skin collagen hydrolyzate had the best IC50 value of 93.32 µg/mL,
categorized as strong antioxidant compounds. The percentage of the degree of
hydrolysis had a correlation with ACE inhibitory activity and antioxidant activity,
with the Pearson correlation coefficient values 0.8592 and -0.4069, respectively. | id |
dc.language.iso | id | id |
dc.publisher | IPB University | id |
dc.title | Aktivitas Antioksidan dan Inhibitor Enzim Pengubah Angiotensin (ACE) Hidrolisat Kolagen Kulit Ikan Nila (Oreochromis niloticus) | id |
dc.title.alternative | Antioxidant and ACE-inhibitory Activities of Tilapia (Oreochromis niloticus) Skin Collagen Hydrolizate | id |
dc.title.alternative | Antioxidant and ACE-inhibitory Activities of Tilapia (Oreochromis niloticus) Skin Collagen Hydrolizate | id |
dc.type | Thesis | id |
dc.subject.keyword | ABTS | id |
dc.subject.keyword | ABTS | id |
dc.subject.keyword | ASC | id |
dc.subject.keyword | degree of hydrolysis | id |
dc.subject.keyword | FTIR | id |
dc.subject.keyword | papain enzyme | id |