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首页> 外文期刊>Journal of Bioinformatics and Sequence Analysis >Towards understanding the regulation of rubber biosynthesis: Insights into the initiator and elongator enzymes
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Towards understanding the regulation of rubber biosynthesis: Insights into the initiator and elongator enzymes

机译:理解橡胶生物合成的调控:对引发剂和延伸剂酶的认识

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Natural rubber is an important polymer produced by plants and made up of isoprene units derived from isopentenyl diphosphate (IPP). Although more than 2000 plant species are known to produce natural rubber, currently there are two important commercial sources,?Hevea brasiliensis (the Brazilian rubber tree) andParthenium argentatum?Gray (guayule). Natural rubber biosynthesis requires three distinct biochemical processes such as (i) initiation, (ii) elongation and (iii) termination.? Computational analyses of the enzymes farnesyl diphosphate (FPP) synthase in?P. argentatum?and cis-prenyl transferase (CPT) in?H. brasiliensis?thatplay a vital role in initiation and elongation stages for biosynthesis of cis-1,4-polyisoprene has been undertaken in this study. Amino acid sequence comparisons of FPP synthase and CPT to their identified similar sequences were carried out to understand the evolutionary relationship among different species.? Homology modeling and binding pocket analysis aided in the understanding of structure-function relationship and enzyme-substrate interaction of FPP synthase and CPT.? The structural templates farnesyl diphosphate synthase (Source:?Gallus gallus) [PDB ID: 1UBX] for FPP synthase and undecaprenyl diphosphate synthase (Source:?Micrococcus luteus?B-P 26) [PDB ID: 1F75] for CPT were selected for homology modeling. The Ramachandran plots were developed for modeled structures of FPP synthase and CPT, which showed 95.9 and 92.6% of amino acid residues occurring in favored regions.? These models were deposited into Protein Model Database [PMDB ID: PM0075218 and PM0075509].? The substrate and cofactor binding site residues of FPP synthase (R103, L149, A184, Y197, L211, H214, E223, T226, D332, K246, Y306, K313) and CPT (Y4, E7, R20, K21, G22, K154, K178, D193, E231, T232, R233) were identified by using binding pocket analysis, which is consistent with available X-ray crystal structure of both the templates. The computational analysis of initiation and elongation for cis-1,4-polyisoprene biosynthesis provided invaluable insights into the identification of putative initiation and elongation factors for FPP synthase and CPT.
机译:天然橡胶是植物生产的重要聚合物,由衍生自二磷酸异戊烯酯(IPP)的异戊二烯单元组成。尽管已知有2000多种植物物种可生产天然橡胶,但目前有两个重要的商业来源,即巴西橡胶树(Hevea brasiliensis)(巴西橡胶树)和阿根廷白蚁(Parthenium argentatum)-灰色(guayule)。天然橡胶的生物合成需要三个不同的生化过程,例如(i)引发,(ii)延伸和(iii)终止。对?P中法呢基二磷酸(FPP)合酶的计算分析。 H中的Argentatum?和顺-异戊二烯基转移酶(CPT)。在这项研究中,巴西利亚在顺式和1,4-聚异戊二烯的生物合成的起始和延伸阶段起着至关重要的作用。为了了解不同物种之间的进化关系,对FPP合酶和CPT与其鉴定的相似序列进行了氨基酸序列比较。同源性建模和结合口袋分析有助于理解FPP合酶和CPT的结构-功能关系和酶-底物相互作用。选择用于FPP合酶的结构模板法呢基二磷酸合酶(来源:?Gallus gallus)[PDB ID:1UBX]和用于CPT的十一碳烯基二磷酸合十一碳烯酸酯(BDB 26)[PDB ID:1F75]用于同源性建模。开发了Ramachandran图以用于FPP合酶和CPT的建模结构,显示95.9和92.6%的氨基酸残基出现在优选区域。这些模型已存入蛋白质模型数据库[PMDB ID:PM0075218和PM0075509]。 FPP合酶(R103,L149,A184,Y197,L211,H214,E223,T226,D332,K246,Y306,K313)和CPT(Y4,E7,R20,K21,G22,K154, K178,D193,E231,T232,R233)是通过使用结合口袋分析法鉴定的,这与两个模板的可用X射线晶体结构一致。 cis-1,4-聚异戊二烯生物合成的起始和延伸的计算分析为鉴定FPP合酶和CPT的假定起始和延伸因子提供了宝贵的见识。

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