HYUNJU KO

Dr. HYUNJU KO

orcid

Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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Verified
Journal Article
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HKHYUNJU KO
HYUNJU KO
SSSu-An Sim
Su-An Sim
MPMi-Hee Park
Mi-Hee Park
HRHwa Sun Ryu
Hwa Sun Ryu
WCWon-Yeong Choi
Won-Yeong Choi
Chang-Gu HyunChang-Gu Hyun
Chang-Gu Hyun
Side streams and byproducts of food are established sources of natural ingredients in cosmetics. In the present study, we obtained upcycled low-molecular-weight anionic peptides (LMAPs) using byproducts of the post-yuzu-juicing process by employing an enzyme derived from Bacillus sp. For the first time, we isolated anionic peptides less than 500 Da in molecular weight from Citrus junos TANAKA seeds via hydrolysis using this enzyme. The protective effect of LMAPs against UVR-induced photoaging was evaluated using a reconstructed skin tissue (RST) model and keratinocytes. The LMAPs protected the keratinocytes by scavenging intracellular reactive oxygen species and by reducing the levels of paracrine cytokines (IL-6 and TNF-α) in UVR (UVA 2 J/cm2 and UVB 15 mJ/cm2)-irradiated keratinocytes. Additionally, the increase in melanin synthesis and TRP-2 expression in RST caused by UVR was significantly inhibited by LMAP treatment. This treatment strongly induced the expression of filaggrin and laminin-5 in UVR-irradiated RST. It also increased type I collagen expression in the dermal region and in fibroblasts in vitro. These results suggest that a hydrolytic system using the enzyme derived from Bacillus sp. can be used for the commercial production of LMAPs from food byproducts and that these LMAPs can be effective ingredients for improving photoaging-induced skin diseases.

Verified
Journal Article
Open access
PDF file
HKHYUNJU KO
HYUNJU KO
SPSeoA Park
SeoA Park
ESEunjin Shin
Eunjin Shin
JKJin Hwa Kim
Jin Hwa Kim
GLGeunsoo Lee
Geunsoo Lee
Chang-Gu HyunChang-Gu Hyun
Chang-Gu Hyun
A novel Bacillus subtilis HB-31 strain was isolated from Gotjawal Wetland in Jeju Island, Republic of Korea. A mucus substance produced by this strain was identified as high-molecular-weight poly-γ-glutamic acid (γ-PGA) using NMR, Fourier transform infrared spectroscopy, and size-exclusion chromatography/multi-angle light scattering analyses. We evaluated whether γ-PGA strengthened the skin barrier using keratinocytes and a reconstructed skin model. In keratinocytes, γ-PGA treatment dose-dependently increased the mRNA expression of skin barrier markers, including filaggrin, involucrin, loricrin, serine palmitoyl transferase, fatty acid synthase, and 3-hydroxy-3-methylglutaryl coenzyme A reductase. γ-PGA also enhanced hyaluronic acid synthesis by upregulating hyaluronic acid synthase-1, -2, and -3 mRNA levels and promoted aquaporin 3 expression, which is involved in skin hydration. In the reconstructed skin model, topical application of 1% γ-PGA elevated filaggrin, involucrin, CD44, and aquaporin 3 expression, compared to the control. These results suggest that the newly isolated HB-31 can be used as a commercial production system of high-molecular-weight γ-PGA, which can serve as an effective ingredient for strengthening the skin barrier and improving moisture retention. Further research is needed to explore the long-term effects of γ-PGA on skin health and its application in treating skin conditions.

18 December 2024 in Preprints.org
Verified
Preprint
Open access
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HKHYUNJU KO
HYUNJU KO
SPSeaA Park
SeaA Park
ESEunjin Shin
Eunjin Shin
JKJin Hwa Kim
Jin Hwa Kim
GLGeunsoo Lee
Geunsoo Lee
Chang-Gu HyunChang-Gu Hyun
Chang-Gu Hyun
A novel Bacillus subtilis HB-31 strain was isolated from Gotjawal Wetland in Jeju Island, Republic of Korea. A mucus substance produced by this strain was identified as high-molecular weight poly-γ-glutamic acid (γ-PGA) using NMR, Fourier transform infrared spectroscopy, and size-exclusion chromatography/multi-angle light scattering analyses. We evaluated whether γ-PGA improved the skin barrier using keratinocytes and reconstructed skin models. In keratinocytes, γ-PGA treatment increased mRNA expression of skin barrier markers, including filaggrin, involucrin, loricrin, serine palmitoyl transferase, fatty acid synthase, and 3-hydroxy-3-methylglutaryl coenzyme A reductase, dose-dependently. γ-PGA also enhanced hyaluronic acid synthesis by upregulating hyaluronic acid synthase-1,-2,and -3 mRNA levels and promoted aquaporin 3 expression, involved in skin hydration. In reconstructed skin models, 1% γ-PGA topical application elevated filaggrin, involucrin, CD44, and aquaporin 3 expression compared to the control. These results suggest that the newly isolated HB-31 can be used as a commercial production system of high-molecular weight γ-PGA, which can be an effective in-gredient for improving skin barrier and moisture. Further research is needed to explore the long-term effects of γ-PGA on skin health and its application in treating skin disorders.