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喜树碱由来自印度马比木的两种内生真菌混合发酵产生。

Camptothecine production by mixed fermentation of two endophytic fungi from Nothapodytes nimmoniana.

作者信息

Bhalkar Bhumika N, Patil Swapnil M, Govindwar Sanjay P

机构信息

Department of Biotechnology, Shivaji University, Kolhapur, 416004, Maharashtra, India.

Department of Biochemistry, Shivaji University, Kolhapur, 416004, Maharashtra, India.

出版信息

Fungal Biol. 2016 Jun-Jul;120(6-7):873-83. doi: 10.1016/j.funbio.2016.04.003. Epub 2016 Apr 12.

Abstract

Two endophytic fungi isolated from the endangered plant Nothapodytes nimmoniana (Grah.) Mabb. were found to effectively synthesize CPT independent of their host plant under submerged fermentation conditions. Molecular characterization of fungi revealed their identity as Colletotrichum fructicola SUK1 (F1) and Corynespora cassiicola SUK2 (F2). Mixed fermentation experiments were carried out to study the effect of microbial signalling between the two fungal species on camptothecine production. Effect of culture parameters on CPT production was studied for both mono-cultures (F1 and F2) separately as well as for the mixed fermentation (F1 + F2). Further the most influencing ones were optimized statistically using response surface methodology. Statistical model based optimized parameters were whey (70 %), agitation rate (110 rpm), temperature (30 °C), and incubation period (7 d) for the mixed fermentation. Monocultures of the two fungal species F1 and F2 yielded CPT up to 33 ± 1.1 mg l(-1)and 69 ± 1.1 mg l(-1), respectively; while their mixed fermentation under the optimized conditions yielded up to 146 ± 0.2 mg l(-1). HPLC and LC-MS/MS techniques were used to analyze the products obtained.

摘要

从濒危植物印度蛇根木(Nothapodytes nimmoniana (Grah.) Mabb.)中分离出的两种内生真菌,被发现在深层发酵条件下能够独立于宿主植物有效合成喜树碱(CPT)。真菌的分子特征鉴定表明,它们分别为果生炭疽菌(Colletotrichum fructicola)SUK1(F1)和多主棒孢(Corynespora cassiicola)SUK2(F2)。进行了混合发酵实验,以研究这两种真菌之间的微生物信号传导对喜树碱产生的影响。分别对单一培养物(F1和F2)以及混合发酵(F1 + F2)研究了培养参数对喜树碱产生的影响。此外,使用响应面法对最具影响的参数进行了统计学优化。基于统计模型优化的混合发酵参数为乳清(70%)、搅拌速度(110 rpm)、温度(30℃)和培养时间(7天)。两种真菌F1和F2的单一培养物分别产生高达33±1.1 mg l⁻¹和69±1.1 mg l⁻¹的喜树碱;而在优化条件下它们的混合发酵产生高达146±0.2 mg l⁻¹的喜树碱。使用高效液相色谱(HPLC)和液相色谱 - 串联质谱(LC-MS/MS)技术分析所获得的产物。

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