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Physiological
properties of Engraulis japonicus muscle protein hydrolysates prepared
by subcritical water hydrolysis
J.S.
Choi1,2, D.B. Jang1, H.E. Moon1, M.K. Roh3,
Y.D. Kim4, K.K. Cho5 and I.S. Choi1,6*
1RIS Center,
Industry-Academic Cooperation Foundation, Silla University, Busan-46958,
Republic of Korea
2Division of
Bioindustry, College of Medical and Life Sciences, Silla University, Busan-46958,
Republic of Korea
3Department of
R&D, Korea Bio & Engineering Co. Ltd., Nam-Gu, Busan-48434, Republic
of Korea
4National Institute
of Fisheries Science, Sanyang-Eup, Tongyeong-Si, Gyeongsangnam-Do-53085,
Republic of Korea
5Department of
Animal Resources Technology, Gyeongnam National University of Science and
Technology, Gyeongnam-52725, Republic of Korea
6Department of Life
Science, Silla University, Busan-46958, Republic of Korea
*Corresponding
Author E-mail: ischoi@silla.ac.kr
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Key
words
Antioxidant activity,
Engraulis japonicus,
Hydrolysate,
Subcritical water hydrolysis,
Tyrosinase inhibitory activity
Publication Data
Paper
received: 14.03.2015
Revised
received: 14.07.2016
Accepted: 12.09.2016
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Abstract
Aim: To evaluate the
beneficial biological activities of Engraulis japonicus muscle
protein, the antioxidant and tyrosinase inhibitory activities of E.
japonicus muscle protein hydrolysates prepared by subcritical water
hydrolysis were investigated.
?
Methodology:
To
evaluate the bioactivity of E. japonicus subcritical hydrolysates, the
applied temperature (pressure) was 140?C (2.6 bar); the reaction times were
0, 5, 10, 15 and 20 min.
Results:
After
10 min of subcritical hydrolysis of particles obtained using 80-200 mesh,
46.39% of the E. japonicus muscle protein was hydrolyzed at 140?C.
According to the response surface methodology results, particles generated
with 80-200 mesh E. japonicus powder exhibited an increased yield of
hydrolysates. The highest DPPH-radical-scavenging activity (34.91%) occurred
in 60-80-mesh sized protein hydrolysates treated at 140?C for 15 min, and the
highest tyrosinase inhibitory activity (99.24%) was identified in 80-200-mesh
sized protein hydrolysates treated at 140?C for 5 min. Changes in the
molecular weight distribution of E. japonicus muscle proteins after
subcritical water hydrolysis were assessed by sodium dodecyl
sulfate-polyacrylamide gel electrophoresis. ????
Interpretation:
Subcritical
water hydrolysis is a suitable technique for generating E. japonicus muscle
protein hydrolysates with useful biological activities, within a short (5?15
min) time frame.
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