• 한국미생물·생명공학회지
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• 제44권2호
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• pp.140-144
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• 2016

사람의 분변으로부터 분리한 Bacteroides stericoris HJ-15로부터 chondroitinase ABC 유전자를 클로닝하였다. 클로닝한 chondroitinase ABC 유전자는 3,090 bp, 1,029 아미노산으로 구성되어 있었다. B. stercoris chondroitinase ABC 유전자는 이미 보고된 chondroitinase ABC 유전자들과 호몰로지가 없었으나, 아미노산서열에서는 82% 호몰로지를 보였다. T7 promoter를 가진 pET-26b+ expression vector에 클로닝한 chondroitinase ABC 유전자를 Escherichia coli BL21 (DE3)에서 발현하여 정제한 재조합 chondroitinase ABC는 chondroitin sulfate A, B 및 C를 모두 분해하였다.

• 생약학회지
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• 제40권2호
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• pp.109-117
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• 2009

We examined the purity of six heparin samples by using heparinase, chondroitinase, $^{1}H-NMR$, and polyacrylamide gel electrophoresis. To obtain high molecular weight contaminants from heparin samples, heparinase I - digested samples were subjected to the exhaustive microcon filtration. The filtration process removed heparin-derived di- and oligosaccharides effectively. By combining chondroitinase ABC treatment and strong anion exchange - high performance liquid chromatography, the result showed all six samples contained chondroitin sulfate as a contaminant ranging from 1.3 to 14.9%. Among them, sample S3 showed the highest content of 14.9%, which was further analyzed by chondroitinase AC treatment to confirm chondroitin sulfate B (dermatan sulfate). $^{1}H-NMR$ chemical shifts of N-acetyl groups clearly suggested the existence of chondroitin sulfate B (sample S3) and oversulfated chondroitin sulfate (samples S2 and S4) as contaminants. In addition, polyacrylamide gel electrophoresis was useful for qualitative detection on the sample's purity. These results suggest that the tools of heparinase I and chondroitinase ABC in combination with NMR spectroscopy would give very useful information for investigation of heparin contaminants such as oversulfated chondroitin sulfate and dermatan sulfate in heparin samples.

• 분석과학
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• 제7권2호
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• pp.245-251
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• 1994

혼합물 중에서 미량 존재하는 황산콘드로이틴나트륨을 정량하기 위하여, Chondroitinase ABC를 사용하여 효소반응을 시킨 후 얻어지는 ${\Delta}Di-6S$(2-acetamido-2-deoxy-3-0-(${\beta}$-D-gluluco-4-enepyranosyluronic acid)-6-0-sulf-D-galactose)를 지표성분을 설정하여 고성능 액체크로마토그래피(HPLC)를 이용하는 방법을 확립하였다. 230nm에서 흡광도를 측정하였고, 검출한계는 $1{\mu}g/ml$였다. 본 분석법을 재제에 적용하였을 때 캅셀제는 $100.01{\pm}1.58%$, 점안제는 $99.89{\pm}1.80%$로 재현성이 있는 결과를 나타내었다.

• 한국식품영양과학회지
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• 제23권6호
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• pp.945-949
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• 1994

Chondroitin sulfate (Chs) contents in edible snail , Achatina fulica Bowdich , andits processed meat extracts were determined by high-performance liquid chormatogrpahy(HPLC) and spectrophotometric method. Spectrophotometric method was based on the precipitation of acriflavine by ChS, and HPLC method was based on the detection of two unsaturated disaccharides, 2-acetamido-2-deoxy-3-O-($\beta$ -D-gluco-4-enepyranosyluronic acid)-4-O-sulfo-D-galactose($\Delta$Di-4S) and 2-acetamido-2deoxy-3-O-($\beta$-D-gluco-4-eepyranosyluronic acid)-6-O-sulfo-D-galactose ($\Delta$야-6S) librated from ChS byenzymeatic digestion with chondroitinase ABc. the ratio of 125$\mu$mol of sodium hydroxide to mg of ChS and 8$0^{\circ}C$ of reaction temperature were proper for alkaline hydrolysis to remove protein residue form ChS. In assay preparation for HPLC ethod, the iptimum concentration of the enzyme chondroitinase ABc was 0.15 unit per 50 $\mu\textrm{g}$ of ChS at a fixed reaction time (30 min) and pH 8.0 using Tris buffer. ChS content in edible snail was 177.6mg% by spectrophotometric method and 153.5mg% by HPLC method and those in the processed meat extract was 71.3mg% by spectrometric method ad 62.8mg% by HPLC method, respectively.

• Restorative Dentistry and Endodontics
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• 제35권3호
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• pp.211-221
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• 2010

본 연구는 상아질의 비교원성 단백질을 chondroitinase ABC (C-ABC)를 이용하여 제거함으로써 비교원성 단백질의 제거가 상아질 접착제의 미세인장결합강도와 교원질망의 형태에 미치는 영향을 상아질의 다양한 습윤상태에 따라 평가하고자 시행하였다. 비교원성 단백질의 상아질접착제의 미세인장강도에 대한 영향을 평가하기 위해 제 3대구치의 상아질을 노출시키고, 두 군으로 나누고 한 군은 C-ABC, 다른 군은 증류수를 $37^{\circ}C$에서 48시간 동안 적용한 후, 상아질의 습윤상태(wet, dry 및 re-wet)와 상아질 접착제(Single Bond 2, One Step Plus)를 다르게 이용하여 복합레진을 수복하였다. 24시간 후 가로 1 mm, 세로 1mm의 시편을 제작하고 미세인장강도를 측정하였다. 상아질 교원질의 형태변화를 관찰하기 위하여 상아질 시편에 산부식을 시행하고 C-ABC 적용 후, 시편을 제작하였고 미세인장강도 측정후 파괴된 접착면의 파괴양상과 각 접착제의 접착계면 관찰을 위하여 FE-SEM 관찰하였다. C-ABC 처리여부와 관계없이 습윤한 상아질면에 접착한 군은 모든 접착제에서 통계학적으로 유의성있는 미세인장결합강도의 차이를 나타나지 않았다(p > 0.05). C-ABC를 적용하였을 경우, Single Bond 2에서는 재수화한 상아질면에 접착한 군이 습윤한 상아질면에 접착한 군에 비해 미세인장결합강도가 감소하였다(p < 0.05). FE-SEM 관찰결과, C-ABC를 적용후에는 접착성 파괴가 주로 일어났으며, 교원질 섬유간 거리가 증가하였으며 부분적으로 교원질 섬유들간에 응집된 양상이 관찰되었다.

• Food Science and Biotechnology
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• 제18권4호
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• pp.872-877
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• 2009

By-products of marine organisms including salmon, skate, flatfish, and yellow goosefish were investigated to search for new source of chondroitin sulfate (CS). Agarose gel electrophoresis with chondroitinase depolymerization showed that purified chondroitin sulfate did not contain any other glycosaminoglycans. 1H-nuclear magnetic resonance (NMR) spectra were acquired to confirm the structure and purity. The average molecular weight ranging from 22 to 64 kDa was determined by high performance size exclusion chromatography. Disaccharide compositions and purities were determined by strong anion exchange-high performance liquid chromatography (SAX-HPLC) after chondroitinase ABC depolymerization. SAX-HPLC data exhibited that the purity was from $81.7{\pm}1.3$ to $114.2{\pm}2.5%$ and the yield was from 1.3 to 12.5%. All analytical results indicate that salmon cartilage, skate cartilage, and yellow goosefish bone could be promising sources of CS to substitute shark cartilage CS in commercial neutraceuticals.

• Archives of Pharmacal Research
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• 제21권5호
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• pp.555-558
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• 1998

chondroitin sulfates were isolated from the mud snail. For the quantitative analysis of enzymatic digestion products of isolated chondroitin sulfates, strong anion exchange-high performance liquid chromatography (SAX-HPLC) was performed. by the action of chondroitinase ABC, three unsaturated disaccharides$ 2-acetamide-2-deoxy-3-O-({\beta}-D-gluco-4-enepyranosyluronic acid)-D-galactose $$({\Delta}Di-OS), $2-acetamide-2-deoxy-3-O-({\beta}-D-gluco-4-enepyranosyluronic acid)-6-O-sulfo-D-galactose ({\Delta}Di-6S) and 2-acetamide-2-deoxy-3-O-({\beta}-D-gluco-4-enepyranosyluronic acid)-4-O-sulfo-D-galactose ({\Delta}Di-4S)$ were produced from the mud snail chondroitin sulfates. The analysis showed that relative proportion of ${\Delta}Di-OS/{\Delta}Di-6S/{\Delta}Di-4S$ was 58.7/3.1/38.2. The immunomodulating activity of chondroitin sulfate was examined by cell proliferation assay and these results suggest that it might be a immunosuppressant.