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Dan-Dan Wang,Yeon-Ju Kim,Nam In Baek,Ramya Mathiyalagan,Chao Wang,Yan Jin,Xing Yue Xu,Deok-Chun Yang 고려인삼학회 2021 Journal of Ginseng Research Vol.45 No.1
Background: Ginsenoside Rh2 is well known for many pharmacological activities, such as anticancer, antidiabetes, antiinflammatory, and antiobesity properties. Glycosyltransferases (GTs) are ubiquitous enzymes present in nature and are widely used for the synthesis of oligosaccharides, polysaccharides, glycoconjugates, and novel derivatives. We aimed to synthesize new ginsenosides from Rh2 using the recombinant GT enzyme and investigate its cytotoxicity with diverse cell lines. Methods: We have used a GT gene with 1,224-bp gene sequence cloned from Lactobacillus rhamnosus (LRGT) and then expressed in Escherichia coli BL21 (DE3). The recombinant GT protein was purified and demonstrated to transform Rh2 into two novel ginsenosides, and they were characterized by nuclear magnetic resonance (NMR) techniques and evaluated by 3-(4, 5-dimethylthiazol-2-yl)-2-5-diphenyltetrazolium bromide assay. Results: Two novel ginsenosides with an additional glucopyranosyl (6/1) and two additional glucopyranosyl (6/1) linked with the C-3 position of the substrate Rh2 were synthesized, respectively. Cell viability assay in the lung cancer (A549) cell line showed that glucosyl ginsenoside Rh2 inhibited cell viability more potently than ginsenoside Rg3 and Rh2 at a concentration of 10 μM. Furthermore, glucosyl ginsenoside Rh2 did not exhibit any cytotoxic effect in murine macrophage cells (RAW264.7), mouse embryo fibroblasts cells (3T3-L1), and skin cells (B16BL6) at a concentration of 10 μM compared with ginsenoside Rh2 and Rg3. Conclusion: This is the first report on the synthesis of two novel ginsenosides, namely, glucosyl ginsenoside Rh2 and diglucosyl ginsenoside Rh2 from Rh2 by using recombinant GT isolated from L. rhamnosus. Moreover, diglucosyl ginsenoside Rh2 might be a new candidate for treatment of inflammation, obesity, and skin whiting, and especially for anticancer.
Wang, Dan-Dan,Jin, Yan,Wang, Chao,Kim, Yeon-Ju,Perez, Zuly Elizabeth Jimenez,Baek, Nam In,Mathiyalagan, Ramya,Markus, Josua,Yang, Deok-Chun The Korean Society of Ginseng 2018 Journal of Ginseng Research Vol.42 No.1
Background: Ginsenoside F1 has been described to possess skin-whitening effects on humans. We aimed to synthesize a new ginsenoside derivative from F1 and investigate its cytotoxicity and melanogenesis inhibitory activity in B16BL6 cells using recombinant glycosyltransferase enzyme. Glycosylation has the advantage of synthesizing rare chemical compounds from common compounds with great ease. Methods: UDP-glycosyltransferase (BSGT1) gene from Bacillus subtilis was selected for cloning. The recombinant glycosyltransferase enzyme was purified, characterized, and utilized to enzymatically transform F1 into its derivative. The new product was characterized by NMR techniques and evaluated by MTT, melanin count, and tyrosinase inhibition assay. Results: The new derivative was identified as (20S)-$3{\beta},6{\alpha},12{\beta}$,20-tetrahydroxydammar-24-ene-20-O-${\beta}$-D-glucopyranosyl-3-O-${\beta}$-D-glucopyranoside(ginsenoside Ia), which possesses an additional glucose linked into the C-3 position of substrate F1. Ia had been previously reported; however, no in vitro biological activity was further examined. This study focused on the mass production of arduous ginsenoside Ia from accessible F1 and its inhibitory effect of melanogenesis in B16BL6 cells. Ia showed greater inhibition of melanin and tyrosinase at $100{\mu}mol/L$ than F1 and arbutin. These results suggested that Ia decreased cellular melanin synthesis in B16BL6 cells through downregulation of tyrosinase activity. Conclusion: To our knowledge, this is the first study to report on the mass production of rare ginsenoside Ia from F1 using recombinant UDP-glycosyltransferase isolated from B. subtillis and its superior melanogenesis inhibitory activity in B16BL6 cells as compared to its precursor. In brief, ginsenoside Ia can be applied for further study in cosmetics.
Multipath Compensation for BPSK Underwater Acoustic Communication
Lin Chun-Dan,Park Ji-Hyun,Yoon Jong Rak The Acoustical Society of Korea 2005 韓國音響學會誌 Vol.24 No.e3
To investigate the equalizer performance in underwater acoustic communication m the presence of intersymbol interference (ISI) due to multipath, computer simulations are carried out in discrete multipath shallow water channels for three different horizontal ranges. For the purpose of computation simplicity, least mean square (LMS) algorithm is adopted both in linear equalizer and nonlinear equalizer, decision feedback equalizer (DFE) to cancel out ISI effects. Binary phase shift keying (BPSK) signals have been transmitted with high data rate of 2000bps through the use of equalization technique. The results demonstrate that equalization is an efficient way to achieve high transmission data rate in the shallow water channel.
Li, Chun-Hong,Liu, Mei-Yan,Liu, Wei,Li, Dan-Dan,Cai, Li Asian Pacific Journal of Cancer Prevention 2014 Asian Pacific journal of cancer prevention Vol.15 No.2
Objective: To observe the short-term efficacy, long-term survival time and adverse responses with nedaplatin (NDP) or cisplatin (DDP) concomitant with other chemotherapy in treating non-small cell lung cancer. Materials and Methods: A retrospective, randomized, control study was conducted, in which 619 NSCLC patients in phases III and IV who were initially treated and re-treated were randomly divided into an NDP group (n=294) and a DDP group (n=325), the latter being regarded as controls. Chemotherapeutic protocols (CP/DP/GP/NP/TP) containing NDP or DDP were given to both groups. Patients in both groups were further divided to evaluate the clinical efficacies according to initial and re-treatment stage, pathological pattern, type of combined chemotherapeutic protocols, tumor stage and surgery. Results: The overall response rate (ORR) and disease control rate (DCR) in the NDP group were 48.6% and 95.2%, significantly higher than in the DDP group at 35.1% and 89.2%, respectively (P<0.01). In NSCLC patients with initial treatment, squamous carcinoma and phase III, there were significant differences in ORR and DCR between the groups (P<0.05), while ORR was significant in patients with adenocarcinoma, GP/TP and in phase IIIa (P<0.05). There was also a significant difference in DCR in patients in phase IIIb (P<0.05). According to the statistical analysis of survival time of all patients and of those in clinical phase III, the NDP group survived significantly longer than the DDP group (P<0.01). The rates of decreased hemoglobin and increased creatinine, nausea and vomiting in the NDP group were evidently lower than in DDP group (P<0.05). Conclusion: NDP concomitant with other chemotherapy is effective for treating NSCLC, with higher clinical efficacy than DDP concomitant with chemotherapy, with advantages in prolonging survival time and reducing toxic and adverse responses.
Lin Chun-Dan,Ro Yong Ju,Rouseff Daniel,Yoon Jong Rak The Acoustical Society of Korea 2005 韓國音響學會誌 Vol.24 No.e2
Experimental work in underwater acoustic communications using passive phase conjugation has shown that the demodulation error depends on the relative drift rate between the source and receiver [Rouseff et al., IEEE J. Oceanic Eng. 26, 821-831 (2001)]. The observed effect involves the mismatch between the initial impulse response and the subsequent response after the source or receiver has changed locations. In the present work, the effect of drifting source is analyzed by numerical simulations and compared to the experimental results. The communications bit error rate is qualified as a function of drift rate, drifting direction, and source-receiver range.
A Statistical Approach for Fast Mode Decision in Scalable Video Coding
Chun-Su Park,Byoung-Kyu Dan,Haechul Choi,Sung-Jea Ko IEEE 2009 IEEE transactions on circuits and systems for vide Vol.19 No.12
<P>In scalable video coding (SVC), an exhaustive mode decision is performed to search for the best mode at each macroblock. Although this method achieves an optimal trade-off between rate and distortion, it introduces an extreme computational burden on the encoder. In this letter, we propose a fast mode decision algorithm that can reduce the computational load of the mode decision for SVC. We statistically derive the expectation of the rate-distortion cost (RDcost) increase caused by skipping each mode in the mode decision. In the proposed algorithm, the encoder performs the mode decision using a small number of modes that are determined based on the expected increase of the RDcost. Experimental results show that the proposed algorithm can reduce the computational complexity significantly with negligible video quality degradation and bitrate increment.</P>