{"title":"喜马拉雅红豆杉(Taxus wallichiana Zucc.)根内生真菌生产紫杉醇","authors":"P. Adhikari, M. Singh, A. Pandey","doi":"10.13052/jgeu0975-1416.1028","DOIUrl":null,"url":null,"abstract":"Taxol® (generic name – Paclitaxel), the most promising chemotherapeutic agent was isolated from bark of different Taxus sp. As Taxus species are threatened with extinction (endangered in Himalaya), thus it is imperative to develop alternate and sustainable method for commercialization and scale up production of paclitaxel. In this respect, physical and chemical parameters are effective and important key points for active compound production particularly by using endophytic microbes. In the present study, five endophytic fungi isolated from the roots of Taxus wallichiana, are tested for paclitaxel production using biochemical and molecular methods. Subsequently, effect of physico-chemical parameters like temperature, pH, incubation time, and medium constituents i.e., salt concentration, carbon and nitrogen sources on paclitaxel production were also analyzed. Among isolates, two of the fungi viz. GBPI_TWR F1 (Penicillium sp.) and GBPI_TWR F5 (Aspergillus sp.) were found to be paclitaxel producing. The genomic DNA samples were sequenced to confirm the presence of two genes viz. 10-deacetylbaccatin III-10-O-acetyl transferase (DBAT) and C-13 phenylpropanoid side chain-CoA acyltransferase (BAPT), implicated in paclitaxel biosynthesis. Both the endophytes showed the amplicons of DBAT and BAPT genes. Results revealed that after optimization of medium components and physical condition, paclitaxel production was increased in both the endophytes, maximum paclitaxel production i.e., 5.45 ± 0.98 mg/L was obtained by GBPI_TWR F5 (Aspergillus sp.) following 10 days of incubation at 15∘C in optimized S7 liquid medium composition.","PeriodicalId":142472,"journal":{"name":"Journal of Graphic Era University","volume":"32 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Production of Taxol by Endophytic Fungi Isolated from Roots of Himalayan Yew (Taxus wallichiana Zucc.)\",\"authors\":\"P. Adhikari, M. Singh, A. Pandey\",\"doi\":\"10.13052/jgeu0975-1416.1028\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Taxol® (generic name – Paclitaxel), the most promising chemotherapeutic agent was isolated from bark of different Taxus sp. 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The genomic DNA samples were sequenced to confirm the presence of two genes viz. 10-deacetylbaccatin III-10-O-acetyl transferase (DBAT) and C-13 phenylpropanoid side chain-CoA acyltransferase (BAPT), implicated in paclitaxel biosynthesis. Both the endophytes showed the amplicons of DBAT and BAPT genes. 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引用次数: 0
摘要
紫杉醇®(通用名- Paclitaxel)是从不同红豆杉(Taxus sp.)的树皮中分离出来的最有前途的化疗药物。由于红豆杉(Taxus)濒临灭绝(在喜马拉雅地区濒临灭绝),因此开发替代和可持续的方法实现紫杉醇的商业化和规模化生产势在必行。在这方面,物理和化学参数是有效的和重要的关键点,特别是利用内生微生物生产活性化合物。本研究从红豆杉(Taxus wallichiana)的根中分离了5种内生真菌,采用生化和分子方法对其产紫杉醇的能力进行了研究。随后,分析了温度、pH、培养时间等理化参数以及培养基成分(盐浓度、碳源和氮源)对紫杉醇生产的影响。在分离株中,发现两种真菌GBPI_TWR F1(青霉菌sp.)和GBPI_TWR F5(曲霉sp.)产生紫杉醇。基因组DNA测序证实了10-去乙酰巴accatin iii -10- o -乙酰转移酶(DBAT)和C-13苯基丙烷侧链辅酶a酰基转移酶(BAPT)两个基因的存在,这两个基因与紫杉醇的生物合成有关。两种内生菌均表现出DBAT和BAPT基因的扩增。结果表明,在优化培养基成分和物理条件后,两种内生菌的紫杉醇产量均有增加,在优化的S7液体培养基中,在15°C下培养10天后,GBPI_TWR F5(曲霉sp.)的紫杉醇产量最高,为5.45±0.98 mg/L。
Production of Taxol by Endophytic Fungi Isolated from Roots of Himalayan Yew (Taxus wallichiana Zucc.)
Taxol® (generic name – Paclitaxel), the most promising chemotherapeutic agent was isolated from bark of different Taxus sp. As Taxus species are threatened with extinction (endangered in Himalaya), thus it is imperative to develop alternate and sustainable method for commercialization and scale up production of paclitaxel. In this respect, physical and chemical parameters are effective and important key points for active compound production particularly by using endophytic microbes. In the present study, five endophytic fungi isolated from the roots of Taxus wallichiana, are tested for paclitaxel production using biochemical and molecular methods. Subsequently, effect of physico-chemical parameters like temperature, pH, incubation time, and medium constituents i.e., salt concentration, carbon and nitrogen sources on paclitaxel production were also analyzed. Among isolates, two of the fungi viz. GBPI_TWR F1 (Penicillium sp.) and GBPI_TWR F5 (Aspergillus sp.) were found to be paclitaxel producing. The genomic DNA samples were sequenced to confirm the presence of two genes viz. 10-deacetylbaccatin III-10-O-acetyl transferase (DBAT) and C-13 phenylpropanoid side chain-CoA acyltransferase (BAPT), implicated in paclitaxel biosynthesis. Both the endophytes showed the amplicons of DBAT and BAPT genes. Results revealed that after optimization of medium components and physical condition, paclitaxel production was increased in both the endophytes, maximum paclitaxel production i.e., 5.45 ± 0.98 mg/L was obtained by GBPI_TWR F5 (Aspergillus sp.) following 10 days of incubation at 15∘C in optimized S7 liquid medium composition.