中国医药生物技术
中國醫藥生物技術
중국의약생물기술
CHINESE MEDICINAL BIOTECHNOLOGY
2014年
3期
180-184
,共5页
蒋忠科%张洋%郭连宏%姜蓉%孙承航
蔣忠科%張洋%郭連宏%薑蓉%孫承航
장충과%장양%곽련굉%강용%손승항
血管内皮生长因子受体2%链霉菌属%胡桃霉素D
血管內皮生長因子受體2%鏈黴菌屬%鬍桃黴素D
혈관내피생장인자수체2%련매균속%호도매소D
Vascular endothelial growth factor receptor-2%streptomyces%Juglomycin D
目的分离鉴定链霉菌 I06A-02754发酵液中具血管内皮生长因子受体-2酪氨酸激酶(VEGFR2-CD)抑制活性的强极性次生代谢产物。<br> 方法采用大孔吸附树脂、阴离子交换树脂、MPLC、HPLC等分离手段对次生代谢产物进行分离纯化;通过 UV、IR、HR-ESI 质谱、1D-NMR 和2D-NMR 对其结构进行鉴定,以 ELISA 法检测其次生代谢产物对 VEGFR2-CD 的抑制活性;以 MTT 法检测化合物对肿瘤细胞的抑制活性。<br> 结果从发酵液的水溶性部分分离得到一个极性较大的胡桃霉素类次生代谢产物--2754R;其化学结构与胡桃霉素D 一致,对 VEGFR2-CD 表现出一定的抑制活性;MTT 实验显示化合物2754R 对 HepG2细胞、MCF-7细胞和BEL-7402细胞没有明显的抑制活性(IC50>10μmol/L)。<br> 结论化合物2754R 是具有 VEGFR2-CD 活性的胡桃霉素类次生代谢产物。
目的分離鑒定鏈黴菌 I06A-02754髮酵液中具血管內皮生長因子受體-2酪氨痠激酶(VEGFR2-CD)抑製活性的彊極性次生代謝產物。<br> 方法採用大孔吸附樹脂、陰離子交換樹脂、MPLC、HPLC等分離手段對次生代謝產物進行分離純化;通過 UV、IR、HR-ESI 質譜、1D-NMR 和2D-NMR 對其結構進行鑒定,以 ELISA 法檢測其次生代謝產物對 VEGFR2-CD 的抑製活性;以 MTT 法檢測化閤物對腫瘤細胞的抑製活性。<br> 結果從髮酵液的水溶性部分分離得到一箇極性較大的鬍桃黴素類次生代謝產物--2754R;其化學結構與鬍桃黴素D 一緻,對 VEGFR2-CD 錶現齣一定的抑製活性;MTT 實驗顯示化閤物2754R 對 HepG2細胞、MCF-7細胞和BEL-7402細胞沒有明顯的抑製活性(IC50>10μmol/L)。<br> 結論化閤物2754R 是具有 VEGFR2-CD 活性的鬍桃黴素類次生代謝產物。
목적분리감정련매균 I06A-02754발효액중구혈관내피생장인자수체-2락안산격매(VEGFR2-CD)억제활성적강겁성차생대사산물。<br> 방법채용대공흡부수지、음리자교환수지、MPLC、HPLC등분리수단대차생대사산물진행분리순화;통과 UV、IR、HR-ESI 질보、1D-NMR 화2D-NMR 대기결구진행감정,이 ELISA 법검측기차생대사산물대 VEGFR2-CD 적억제활성;이 MTT 법검측화합물대종류세포적억제활성。<br> 결과종발효액적수용성부분분리득도일개겁성교대적호도매소류차생대사산물--2754R;기화학결구여호도매소D 일치,대 VEGFR2-CD 표현출일정적억제활성;MTT 실험현시화합물2754R 대 HepG2세포、MCF-7세포화BEL-7402세포몰유명현적억제활성(IC50>10μmol/L)。<br> 결론화합물2754R 시구유 VEGFR2-CD 활성적호도매소류차생대사산물。
Objective To discover antagonists of VEGFR2-CD from the fermentation broth produced by streptomyces strain I06A-02754. <br> Methods Under guidance of ELISA assay against VEGFR2-CD, compound 2754R was isolated and purified by combination of different column chromatographies and HPLC. The structure of compound 2754R was identified by combination of analysis of UV, IR, HR-ESI-MS and 1D-NMR, 2D-NMR. The cytotoxicity of compound 2754R was tested by MTT assay. <br> Results Compound 2754R was purified and structurally identified as Juglomycin group antibiotics, and was the same with Juglomycin D. Compound 2754R showed weak antagonistic activity against VEGFR2-CD by ELISA assay, but did not show obvious cytotoxicity on HepG2 (human hepatocellular carcinoma), BEL-7402 (human hepatocellular carcinoma) and MCF-7 (human breast cancer) cell lines at 10μmol/L. <br> Conclusion It is firstly reported compound 2754R (Juglomycin D) has antagonistic activity against VEGFR2-CD.