中国医药导报
中國醫藥導報
중국의약도보
China Medical Herald
2015年
31期
53-56
,共4页
申丽%秦云%李明%王晶%傅奕%王凤舞
申麗%秦雲%李明%王晶%傅奕%王鳳舞
신려%진운%리명%왕정%부혁%왕봉무
裙带菜%内生菌%化学成分%环二肽%乙酰胆碱酯酶抑制活性
裙帶菜%內生菌%化學成分%環二肽%乙酰膽堿酯酶抑製活性
군대채%내생균%화학성분%배이태%을선담감지매억제활성
Undaria pinnatifida%Endophyte%Chemical constituent%Cyclic dipeptide%AChE inhibitory activity
目的:研究裙带菜内生菌Bac illus sp. QD-4发酵液的化学成分。方法采用硅胶柱层析、羟丙基葡聚糖凝胶柱层析、薄层层析、反相高效液相色谱等方法对QD-4发酵液乙酸乙酯提取物进行分离纯化,并采用质谱、核磁共振谱等技术及文献比对的方法对化合物进行结构鉴定;采用改良Ellman法测定化合物对乙酰胆碱酯酶(AChE)的抑制活性。结果从QD-4发酵液乙酸乙酯提取物中分离得到5种化合物:环-(L-亮氨酸-L-4-羟脯氨酸)(1)、环-(L-脯氨酸-L-酪氨酸)(2)、环-(甘氨酸-L-脯氨酸)(3)、环-(L-脯氨酸-D-酪氨酸)(4)和尿嘧啶(5)。在400μg/mL浓度下,化合物2和4对AChE的抑制率分别为(11.62±2.29)%和(5.62±1.63)%。结论化合物2和4对AchE具有一定的抑制活性,是Bacillus sp. QD-4发酵液抑制AChE活性的物质基础。
目的:研究裙帶菜內生菌Bac illus sp. QD-4髮酵液的化學成分。方法採用硅膠柱層析、羥丙基葡聚糖凝膠柱層析、薄層層析、反相高效液相色譜等方法對QD-4髮酵液乙痠乙酯提取物進行分離純化,併採用質譜、覈磁共振譜等技術及文獻比對的方法對化閤物進行結構鑒定;採用改良Ellman法測定化閤物對乙酰膽堿酯酶(AChE)的抑製活性。結果從QD-4髮酵液乙痠乙酯提取物中分離得到5種化閤物:環-(L-亮氨痠-L-4-羥脯氨痠)(1)、環-(L-脯氨痠-L-酪氨痠)(2)、環-(甘氨痠-L-脯氨痠)(3)、環-(L-脯氨痠-D-酪氨痠)(4)和尿嘧啶(5)。在400μg/mL濃度下,化閤物2和4對AChE的抑製率分彆為(11.62±2.29)%和(5.62±1.63)%。結論化閤物2和4對AchE具有一定的抑製活性,是Bacillus sp. QD-4髮酵液抑製AChE活性的物質基礎。
목적:연구군대채내생균Bac illus sp. QD-4발효액적화학성분。방법채용규효주층석、간병기포취당응효주층석、박층층석、반상고효액상색보등방법대QD-4발효액을산을지제취물진행분리순화,병채용질보、핵자공진보등기술급문헌비대적방법대화합물진행결구감정;채용개량Ellman법측정화합물대을선담감지매(AChE)적억제활성。결과종QD-4발효액을산을지제취물중분리득도5충화합물:배-(L-량안산-L-4-간포안산)(1)、배-(L-포안산-L-락안산)(2)、배-(감안산-L-포안산)(3)、배-(L-포안산-D-락안산)(4)화뇨밀정(5)。재400μg/mL농도하,화합물2화4대AChE적억제솔분별위(11.62±2.29)%화(5.62±1.63)%。결론화합물2화4대AchE구유일정적억제활성,시Bacillus sp. QD-4발효액억제AChE활성적물질기출。
Objective To study chemical constituents of liquid culture of endophyte Bac illus sp. QD-4 from Undaria pinnatifida. Methods Isolation and purification of EtOAc extract of liquid culture of QD-4 was performed through silica gel chromatograph, gel filtration over Sephadex LH-20, TLC and RP-HPLC and structures of obtained compounds were elucidated by spectral techniques such as mass spectrum, NMR spectra and comparison with literatures. Acetylc-holesterase (AChE) inhibitory activity of compounds was evaluated by modified Ellman method. Results Five com-pounds were isolated from the EtOAc extract of liquid culture of strain QD-4 and identified as cyclo-(L-Leu-L-4-hy-droxy-Pro) (1), cyclo-(L-Pro-L-Tyr) (2), cyclo-(Gly-L-Pro) (3), cyclo-(L-Pro-D-Tyr) (4) and uracil (5) respectively. At concentration of 400 μg/mL, compounds 2 and 4 were found to inhibit acetylcholesterase with inhibition rate of (11.62±2.29)% and (5.62±1.63)%respectively. Conclusion Compounds 2 and 4 can inhibit acetylcholesterase to some extent, which is material basis of liquid culture of Bacillus sp. QD-4 for AChE inhibitory activity.