Identification and characterization of type III polyketide synthase genes from culturable endophytes of ethnomedicinal plants

被引:0
|
作者
Manoharan, Gomathi [1 ]
Sairam, Thiagarajan [1 ]
Thangamani, Rajesh [2 ]
Ramakrishnan, Dhivya [1 ]
Tiwari, Manish K. [3 ]
Lee, Jung-Kul [4 ]
Marimuthu, Jeya [1 ,5 ]
机构
[1] PSG Inst Med Sci & Res, PSG Ctr Mol Med & Therapeut, Coimbatore 641004, Tamil Nadu, India
[2] CSIR Natl Engn & Environm Res Inst, CMC, Biotechnol Div, Chennai 600113, Tamil Nadu, India
[3] Univ Copenhagen, Dept Chem, Univ Pk 5, DK-2100 Copenhagen, Denmark
[4] Konkuk Univ, Dept Chem Engn, Seoul 05029, South Korea
[5] Natl Inst Ocean Technol, Marine Biotechnol Div, Chennai 600100, Tamil Nadu, India
基金
新加坡国家研究基金会;
关键词
Bacopamonnieri; Fungal endophyte; Fusarium incarnatum; CODEHOP PCR; Type III polyketide synthase; BACOPA-MONNIERA; FUNGI; DIVERSITY;
D O I
10.1016/j.enzmictec.2019.10939
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Endophytic fungi provide benefits to host plants by producing a diverse class of secondary metabolites (natural products). Arrays of polyketide natural products are synthesized by specific classes of polyketide synthases (PKS I, II and III) in host organisms. In the present study, we attempt to screen and identify type HI PKSs in culturable fungal endophytes isolated from the ethno medicinal plants including Arbus precatorius, Bacopa monnieri,Citrus aurantifolia and Datura metel to detect the genetic potential of endophytic fungi in producing bioactive compounds. A total of seventeen endophytic fungal strains belonging to eight genera were identified using fungal morphology and rDNA-ITS phylogenetic analyses. A CODEHOP-PCR based strategy was followed to design degenerate primers for the screening of type III PKS genes from fungal endophytes. We had successfully amplified partial PKS genes from eight endophytes. The amplified PKS sequences showed 60-99% identity to already characterized/putative PKS genes. From the partial sequence of FiPKS from Fusarium incarnatum BMER1, a full-length gene was amplified, cloned and characterized. FiPKScDNA was cloned and expressed in E. coil Lemo21 (DE3) and the purified protein was shown to produce pyrones and resorcinols using acyl-CoA thioesters as substrates. FiPKS showed the highest catalytic efficiency of 7.6 x 10(4) s(-1) M-1 with stearoyl CoA as a starter unit. This study reports the identification and characterization of type III PKS from endophytes of medicinal plants by CODEHOP PCR.
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页数:6
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