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真菌聚酮合酶中产物释放酶结构域的序列、结构及功能分析

Analysis of the Sequences, Structures, and Functions of Product-Releasing Enzyme Domains in Fungal Polyketide Synthases.

作者信息

Liu Lu, Zhang Zheng, Shao Chang-Lun, Wang Chang-Yun

机构信息

Key Laboratory of Marine Drugs, The Ministry of Education of China, School of Medicine and Pharmacy, Ocean University of ChinaQingdao, China.

Laboratory for Marine Drugs and Bioproducts, Qingdao National Laboratory for Marine Science and TechnologyQingdao, China.

出版信息

Front Microbiol. 2017 Sep 4;8:1685. doi: 10.3389/fmicb.2017.01685. eCollection 2017.

Abstract

Product-releasing enzyme (PRE) domains in fungal non-reducing polyketide synthases (NR-PKSs) play a crucial role in catalysis and editing during polyketide biosynthesis, especially accelerating final biosynthetic reactions accompanied with product offloading. However, up to date, the systematic knowledge about PRE domains is deficient. In the present study, the relationships between sequences, structures, and functions of PRE domains were analyzed with 574 NR-PKSs of eight groups (I-VIII). It was found that the PRE domains in NR-PKSs could be mainly classified into three types, thioesterase (TE), reductase (R), and metallo-β-lactamase-type TE (MβL-TE). The widely distributed TE or TE-like domains were involved in NR-PKSs of groups I-IV, VI, and VIII. The R domains appeared in NR-PKSs of groups IV and VII, while the physically discrete MβL-TE domains were employed by most NR-PKSs of group V. The changes of catalytic sites and structural characteristics resulted in PRE functional differentiations. The phylogeny revealed that the evolution of TE domains was accompanied by complex functional divergence. The diverse sequence lengths of TE lid-loops affected substrate specificity with different chain lengths. The volume diversification of TE catalytic pockets contributed to catalytic mechanisms with functional differentiations. The above findings may help to understand the crucial catalysis of fungal aromatic polyketide biosyntheses and govern recombination of NR-PKSs to obtain unnatural target products.

摘要

真菌非还原型聚酮合酶(NR-PKSs)中的产物释放酶(PRE)结构域在聚酮生物合成过程中的催化和编辑中起着关键作用,特别是加速最终生物合成反应并伴随着产物卸载。然而,迄今为止,关于PRE结构域的系统知识还很缺乏。在本研究中,利用八组(I-VIII)的574个NR-PKSs分析了PRE结构域的序列、结构和功能之间的关系。发现NR-PKSs中的PRE结构域主要可分为三种类型,硫酯酶(TE)、还原酶(R)和金属β-内酰胺酶型TE(MβL-TE)。广泛分布的TE或TE样结构域参与了I-IV、VI和VIII组的NR-PKSs。R结构域出现在IV和VII组的NR-PKSs中,而物理上离散的MβL-TE结构域被V组的大多数NR-PKSs所采用。催化位点和结构特征的变化导致了PRE功能的分化。系统发育分析表明,TE结构域的进化伴随着复杂的功能分歧。TE盖子环的不同序列长度影响了不同链长底物的特异性。TE催化口袋的体积多样化促成了具有功能分化的催化机制。上述发现可能有助于理解真菌芳香聚酮生物合成的关键催化作用,并控制NR-PKSs的重组以获得非天然目标产物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed7b/5591372/95e3a38ea0fd/fmicb-08-01685-g001.jpg

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