自抗性基因导向的活性天然产物挖掘

宋永相; 张秀凤; 李艳芹; 肖华; 闫岩

doi:10.12211/2096-8280.2023-099

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自抗性基因导向的活性天然产物挖掘

特约评述 | 更新时间：2025-03-19

- 自抗性基因导向的活性天然产物挖掘
- Resistance-gene directed discovery of bioactive natural products
- 合成生物学 2024年5卷第3期页码：474-491
- 作者机构：
  
  1.中国科学院热带海洋生物资源与生态重点实验室，广东省海洋药物重点实验室，中国科学院南海生态环境工程创新研究院，中国科学院南海海洋研究所，广东广州 510301
  2.三亚海洋生态环境工程研究院，海南三亚 572000
  3.中国科学院大学，北京 100049
- 作者简介：
  
  [ "宋永相（1980—），男，博士，副研究员。研究方向为海洋微生物活性物质的发掘与应用。E-mail：songx@scsio.ac.cn" ]
  [ "闫岩（1986—），男，博士，研究员。研究方向为海洋活性天然产物的挖掘与合成生物学智造。E-mail：yyan@scsio.ac.cn" ]
- 基金信息：
  
  国家自然科学基金(32000044);国家重点研发计划(2022YFC2805000);海南省科技计划三亚崖州湾科技城联合项目(2021CXLH0013)
- DOI：10.12211/2096-8280.2023-099
  中图分类号： Q819
- 收稿：2023-12-01，
  
  修回：2024-03-08，
  
  纸质出版：2024-06-30
- 稿件说明：
移动端阅览
宋永相，张秀凤，李艳芹，肖华，闫岩. 自抗性基因导向的活性天然产物挖掘［J］. 合成生物学， 2024， 5（3）： 474-491

SONG Yongxiang， ZHANG Xiufeng， LI Yanqin， XIAO Hua， YAN Yan. Resistance-gene directed discovery of bioactive natural products［J］. Synthetic Biology Journal， 2024， 5（3）： 474-491
宋永相，张秀凤，李艳芹，肖华，闫岩. 自抗性基因导向的活性天然产物挖掘［J］. 合成生物学， 2024， 5（3）： 474-491 DOI： 10.12211/2096-8280.2023-099.

SONG Yongxiang， ZHANG Xiufeng， LI Yanqin， XIAO Hua， YAN Yan. Resistance-gene directed discovery of bioactive natural products［J］. Synthetic Biology Journal， 2024， 5（3）： 474-491 DOI： 10.12211/2096-8280.2023-099.

摘要

天然产物是医药与农药的重要来源。基因组测序和生物信息学分析技术的飞速发展，揭示了大量功能未知的天然产物生物合成基因簇，利用生物信息学工具，从这些庞大的基因簇数据中挖掘活性天然产物已经成为发现新型天然药物的重要途径。天然产物的生产者们利用自抗性基因所表达的自抗性酶来保护自身，这种自抗性酶是体内一些初级代谢途径中管家酶的变体，不但对于活性天然产物具有较好的耐受性，还可以在生产活性天然产物的同时确保宿主体内代谢的正常进行。因而，自抗性基因指导的天然产物研究有效地将活性导向和基因组导向的天然产物发掘策略桥连起来，为精准发掘具有目标活性的新型天然产物提供了有效策略。本文对利用自抗性基因作为探针进行天然产物发掘的代表性研究工作进行了整理和总结，并对研究趋势进行了展望，主要包括：①对于活性已知的天然产物，利用其自抗性基因来定位生物合成基因簇的研究；②以天然产物生物合成基因簇中的自抗性基因为线索，预测产物的作用靶点的研究；③利用天然产物自抗性机制，将具有已知作用机制的活性分子进行快速排重的研究；④利用自抗性基因与天然产物及其活性的内在联系，以目标靶点导向的活性天然产物基因组挖掘；⑤自抗性基因导向的基因组数据挖掘工具的发展情况。

Abstract

Natural products play a crucial role as sources of therapeutic agents for human being and agricultural pesticides. With the development of sequencing technologies

genome mining employing various bioinformatic tools has become an important approach for discovering more natural products. Due to the large number of natural product biosynthetic gene clusters

screening those capable of generating the most potent bioactive molecules has gained significance. To avoid self-destruction

some bioactive molecule producers have evolved with self-resistance enzymes

which are slightly mutated versions of original enzymes

but not sensitive to the bioactive compounds. The presence of self-resistance enzymes in the biosynthetic gene cluster of natural products serves as an indicator for the biosynthesis of bioactive compounds. On the other hand

the biosynthetic gene clusters of natural products could be located using information with their structures and activities as probes

. the accumulating knowledge on antibiotic resistance mechanisms has facilitated the discovery of new antibiotics. Moreover

dereplication of natural products with known resistance mechanisms has been achieved by using indicator strains expressing the resistance genes. While these approaches have successfully utilized self-resistance genes to connect molecules with their biological activities

a more impactful application is to accurately link biological activity with genomic information through target-guided mining of natural products. The concept is to use a self-resistance gene as a predictive tool to screen and identify biosynthetic gene clusters encoding compounds that inhibit specific targets. Recent breakthroughs in self-resistance gene ide

ntification have bridged the gap between activity-guided and genome-driven approaches for natural product discovery and functional assignment. This review summarizes progress in bioactive natural product discovery guided by self-resistance genes

as well as its applications

which include the following points: 1) locating biosynthetic gene clusters based on self-resistance genes

2) predicting the targets of secondary metabolites through self-resistance genes

3) rapid dereplication of bioactive compounds with self-resistance mechanisms

4) genome mining of bioactive natural products guided by the target and the internal connection with self-resistance genes

and 5) the development of genome data mining tools directed by self-resistance genes.

关键词

Keywords

references

NEWMAN D J , CRAGG G M . Natural products as sources of new drugs over the nearly four decades from 01/1981 to 09/2019 [J ] . Journal of Natural Products , 2020 , 83 ( 3 ): 770 - 803 .

ATANASOV A G , ZOTCHEV S B , DIRSCH V M , et al . Natural products in drug discovery: advances and opportunities [J ] . Nature Reviews Drug Discovery , 2021 , 20 ( 3 ): 200 - 216 .

CANTRELL C L , DAYAN F E , DUKE S O . Natural products as sources for new pesticides [J ] . Journal of Natural Products , 2012 , 75 ( 6 ): 1231 - 1242 .

YAN Y , LIU Q K , JACOBSEN S E , et al . The impact and prospect of natural product discovery in agriculture: new technologies to explore the diversity of secondary metabolites in plants and microorganisms for applications in agriculture [J ] . EMBO Reports , 2018 , 19 ( 11 ): e46824 .

DAYAN F E , DUKE S O . Natural compounds as next-generation herbicides [J ] . Plant Physiology , 2014 , 166 ( 3 ): 1090 - 1105 .

DAYAN F E , OWENS D K , DUKE S O . Rationale for a natural products approach to herbicide discovery [J ] . Pest Management Science , 2012 , 68 ( 4 ): 519 - 528 .

SONG C G , YANG J , ZHANG M Z , et al . Marine natural products: the important resource of biological insecticide [J ] . Chemistry & Biodiversity , 2021 , 18 ( 5 ): e2001020 .

HENKE M T , KELLEHER N L . Modern mass spectrometry for synthetic biology and structure-based discovery of natural products [J ] . Natural Product Reports , 2016 , 33 ( 8 ): 942 - 950 .

DUKE S O , ROMAGNI J G , DAYAN F E . Natural products as sources for new mechanisms of herbicidal action [J ] . Crop Protection , 2000 , 19 ( 8-10 ): 583 - 589 .

DAYAN F E , CANTRELL C L , DUKE S O . Natural products in crop protection [J ] . Bioorganic & Medicinal Chemistry , 2009 , 17 ( 12 ): 4022 - 4034 .

CRAGG G M , NEWMAN D J , SNADER K M . Natural products in drug discovery and development [J ] . Journal of Natural Products , 1997 , 60 ( 1 ): 52 - 60 .

MULLOWNEY M W , DUNCAN K R , ELSAYED S S , et al . Artificial intelligence for natural product drug discovery [J ] . Nature Reviews Drug Discovery , 2023 , 22 ( 11 ): 895 - 916 .

CHOPRA B , DHINGRA A K . Natural products: a lead for drug discovery and development [J ] . Phytotherapy Research , 2021 , 35 ( 9 ): 4660 - 4702 .

NEWMAN D J , CRAGG G M . Natural products as sources of new drugs over the 30 years from 1981 to 2010 [J ] . Journal of Natural Products , 2012 , 75 ( 3 ): 311 - 335 .

NEWMAN D J , CRAGG G M , SNADER K M . The influence of natural products upon drug discovery [J ] . Natural Product Reports , 2000 , 17 ( 3 ): 215 - 234 .

LOBANOVSKA M , PILLA G . Penicillin’s discovery and antibiotic resistance: lessons for the future? [J ] . The Yale Journal of Biology and Medicine , 2017 , 90 ( 1 ): 135 - 145 .

NÜTZMANN H W , SCAZZOCCHIO C , OSBOURN A . Metabolic gene clusters in eukaryotes [J ] . Annual Review of Genetics , 2018 , 52 : 159 - 183 .

FISCHBACH M A , WALSH C T . Assembly-line enzymology for polyketide and nonribosomal peptide antibiotics: logic, machinery, and mechanisms [J ] . Chemical Reviews , 2006 , 106 ( 8 ): 3468 - 3496 .

ROBBINS T , LIU Y C , CANE D E , et al . Structure and mechanism of assembly line polyketide synthases [J ] . Current Opinion in Structural Biology , 2016 , 41 : 10 - 18 .

SÜSSMUTH R D , MAINZ A . Nonribosomal peptide synthesis-principles and prospects [J ] . Angewandte Chemie International Edition , 2017 , 56 ( 14 ): 3770 - 3821 .

CHRISTIANSON D W . Structural and chemical biology of terpenoid cyclases [J ] . Chemical Reviews , 2017 , 117 ( 17 ): 11570 - 11648 .

RUDOLF J D , CHANG C Y . Terpene synthases in disguise: enzymology, structure, and opportunities of non-canonical terpene synthases [J ] . Natural Product Reports , 2020 , 37 ( 3 ): 425 - 463 .

KIM H U , BLIN K , LEE S Y , et al . Recent development of computational resources for new antibiotics discovery [J ] . Current Opinion in Microbiology , 2017 , 39 : 113 - 120 .

MEDEMA M H , FISCHBACH M A . Computational approaches to natural product discovery [J ] . Nature Chemical Biology , 2015 , 11 ( 9 ): 639 - 648 .

RUTLEDGE P J , CHALLIS G L . Discovery of microbial natural products by activation of silent biosynthetic gene clusters [J ] . Nature Reviews Microbiology , 2015 , 13 ( 8 ): 509 - 523 .

CIMERMANCIC P , MEDEMA M H , CLAESEN J , et al . Insights into secondary metabolism from a global analysis of prokaryotic biosynthetic gene clusters [J ] . Cell , 2014 , 158 ( 2 ): 412 - 421 .

WALSH C T , FISCHBACH M A . Natural products version 2.0: connecting genes to molecules [J ] . Journal of the American Chemical Society , 2010 , 132 ( 8 ): 2469 - 2493 .

HARVEY A L , EDRADA-EBEL R , QUINN R J . The re-emergence of natural products for drug discovery in the genomics era [J ] . Nature Reviews Drug Discovery , 2015 , 14 ( 2 ): 111 - 129 .

VAN LANEN S G , SHEN B . Microbial genomics for the improvement of natural product discovery [J ] . Current Opinion in Microbiology , 2006 , 9 ( 3 ): 252 - 260 .

LAUTRU S , DEETH R J , BAILEY L M , et al . Discovery of a new peptide natural product by Streptomyces coelicolor genome mining [J ] . Nature Chemical Biology , 2005 , 1 ( 5 ): 265 - 269 .

CLEVENGER K D , BOK J W , YE R , et al . A scalable platform to identify fungal secondary metabolites and their gene clusters [J ] . Nature Chemical Biology , 2017 , 13 ( 8 ): 895 - 901 .

ZHANG J J , TANG X Y , MOORE B S . Genetic platforms for heterologous expression of microbial natural products [J ] . Natural Product Reports , 2019 , 36 ( 9 ): 1313 - 1332 .

HOPWOOD D A . Genetic contributions to understanding polyketide synthases [J ] . Chemical Reviews , 1997 , 97 ( 7 ): 2465 - 2498 .

SCHERLACH K , HERTWECK C . Mining and unearthing hidden biosynthetic potential [J ] . Nature Communications , 2021 , 12 ( 1 ): 3864 .

BAUMAN K D , BUTLER K S , MOORE B S , et al . Genome mining methods to discover bioactive natural products [J ] . Natural Product Reports , 2021 , 38 ( 11 ): 2100 - 2129 .

ZIEMERT N , ALANJARY M , WEBER T . The evolution of genome mining in microbes—a review [J ] . Natural Product Reports , 2016 , 33 ( 8 ): 988 - 1005 .

杨谦 , 程伯涛 , 汤志军 , 等 . 基因组挖掘在天然产物发现中的应用和前景 [J ] . 合成生物学 , 2021 , 2 ( 5 ): 697 - 715 .

YANG Q , CHENG B T , TANG Z J , et al . Applications and prospects of genome mining in the discovery of natural products [J ] . Synthetic Biology Journal , 2021 , 2 ( 5 ): 697 - 715 .

GALM U , HAGER M H , VAN LANEN S G , et al . Antitumor antibiotics: bleomycin, enediynes, and mitomycin [J ] . Chemical Reviews , 2005 , 105 ( 2 ): 739 - 758 .

WEISBLUM B . Erythromycin resistance by ribosome modification [J ] . Antimicrobial Agents and Chemotherapy , 1995 , 39 ( 3 ): 577 - 585 .

YAN Y , LIU N , TANG Y . Recent developments in self-resistance gene directed natural product discovery [J ] . Natural Product Reports , 2020 , 37 ( 7 ): 879 - 892 .

ALMABRUK K H , DINH L K , PHILMUS B . Self-resistance of natural product producers: past, present, and future focusing on self-resistant protein variants [J ] . ACS Chemical Biology , 2018 , 13 ( 6 ): 1426 - 1437 .

O'NEILL E C , SCHORN M , LARSON C B , et al . Targeted antibiotic discovery through biosynthesis-associated resistance determinants: target directed genome mining [J ] . Critical Reviews in Microbiology , 2019 , 45 ( 3 ): 255 - 277 .

STANCU C , SIMA A . Statins: mechanism of action and effects [J ] . Journal of Cellular and Molecular Medicine , 2001 , 5 ( 4 ): 378 - 387 .

CHAMILOS G , LEWIS R E , KONTOYIANNIS D P . Lovastatin has significant activity against zygomycetes and interacts synergistically with voriconazole [J ] . Antimicrobial Agents and Chemotherapy , 2006 , 50 ( 1 ): 96 - 103 .

HUTCHINSON C R , KENNEDY J , PARK C , et al . Aspects of the biosynthesis of non-aromatic fungal polyketides by iterative polyketide synthases [J ] . Antonie Van Leeuwenhoek , 2000 , 78 ( 3-4 ): 287 - 295 .

STEFFENSKY M , MÜHLENWEG A , WANG Z X , et al . Identification of the novobiocin biosynthetic gene cluster of Streptomyces spheroides NCIB 11891 [J ] . Antimicrobial Agents and Chemotherapy , 2000 , 44 ( 5 ): 1214 - 1222 .

WANG Z X , LI S M , HEIDE L . Identification of the coumermycin A(1) biosynthetic gene cluster of Streptomyces rishiriensis DSM 40489 [J ] . Antimicrobial Agents and Chemotherapy , 2000 , 44 ( 11 ): 3040 - 3048 .

BENTLEY R . Mycophenolic acid: a one hundred year odyssey from antibiotic to immunosuppressant [J ] . Chemical Reviews , 2000 , 100 ( 10 ): 3801 - 3826 .

REGUEIRA T B , KILDEGAARD K R , HANSEN B G , et al . Molecular basis for mycophenolic acid biosynthesis in Penicillium brevicompactum [J ] . Applied and Environmental Microbiology , 2011 , 77 ( 9 ): 3035 - 3043 .

LIN H C , CHOOI Y H , DHINGRA S , et al . The fumagillin biosynthetic gene cluster in Aspergillus fumigatus encodes a cryp tic terpene cyclase involved in the formation of β- trans -bergamotene [J ] . Journal of the American Chemical Society , 2013 , 135 ( 12 ): 4616 - 4619 .

BIRCH A J , HUSSAIN S F . Studies in relation to biosynthesis. Part ⅩⅩⅩⅧ. A preliminary study of fumagillin [J ] . Journal of the Chemical Society C: Organic , 1969 ( 11 ): 1473 .

LIU S , WIDOM J , KEMP C W , et al . Structure of human methionine aminopeptidase-2 complexed with fumagillin [J ] . Science , 1998 , 282 ( 5392 ): 1324 - 1327 .

CAMPOY S , ADRIO J L . Antifungals [J ] . Biochemical Pharmacology , 2017 , 133 : 86 - 96 .

DA SILVA FERREIRA M E , COLOMBO A L , PAULSEN I , et al . The ergosterol biosynthesis pathway, transporter genes, and azole resistance in Aspergillus fumigatus [J ] . Medical Mycology , 2005 , 43 ( Suppl 1 ): S313 - S319 .

LIU N , ABRAMYAN E D , CHENG W , et al . Targeted genome mining reveals the biosynthetic gene clusters of natural product CYP51 inhibitors [J ] . Journal of the American Chemical Society , 2021 , 143 ( 16 ): 6043 - 6047 .

MATTHEUS W , MASSCHELEIN J , GAO L J , et al . The kalimantacin/batumin biosynthesis operon encodes a self-resistance isoform of the FabⅠ bacterial target [J ] . Chemistry & Biology , 2010 , 17 ( 10 ): 1067 - 1071 .

HEATH R J , ROCK C O . A triclosan-resistant bacterial enzyme [J ] . Nature , 2000 , 406 ( 6792 ): 145 - 146 .

TOYOHARA M . Aspects of the antituberculous activity of 27753-RP, a new semisynthetic derivative of griselimycine [J ] . Annales de L’Institut Pasteur Microbiology , 1987 , 138 ( 6 ): 737 - 744 .

HOAGLAND D T , LIU J Y , LEE R B , et al . New agents for the treatment of drug-resistant Mycobacterium tuberculosis [J ] . Advanced Drug Delivery Reviews , 2016 , 102 : 55 - 72 .

KLING A , LUKAT P , ALMEIDA D V , et al . Antibiotics. Targeting DnaN for tuberculosis therapy using novel griselimycins [J ] . Science , 2015 , 348 ( 6239 ): 1106 - 1112 .

VINALE F , FLEMATTI G , SIVASITHAMPARAM K , et al . Harzianic acid, an antifungal and plant growth promoting metabolite from Trichoderma harzianum [J ] . Journal of Natural Products , 2009 , 72 ( 11 ): 2032 - 2035 .

LONHIENNE T , LOW Y S , GARCIA M D , et al . Structures of fungal and plant acetohydroxyacid synthases [J ] . Nature , 2020 , 586 ( 7828 ): 317 - 321 .

XIE L N , ZANG X , CHENG W , et al . Harzianic acid from Trichoderma afroharzianum is a natural product inhibitor of acetohydroxyacid synthase [J ] . Journal of the American Chemical Society , 2021: , 143 ( 25 ): 9575 - 9584 .

MCCOURT J A , DUGGLEBY R G . Acetohydroxyacid synthase and its role in the biosynthetic pathway for branched-chain amino acids [J ] . Amino Acids , 2006 , 31 ( 2 ): 173 - 210 .

JASTRZĘBOWSKA K , GABRIEL I . Inhibitors of amino acids biosynthesis as antifungal agents [J ] . Amino Acids , 2015 , 47 ( 2 ): 227 - 249 .

ZHONG B F , WAN J , SHANG C H , et al . Biosynthesis of rumbrins and inspiration for discovery of HIV inhibitors [J ] . Acta Pharmaceutica Sinica B , 2022 , 12 ( 11 ): 4193 - 4203 .

LIU L X , MARGOTTIN F , LE GALL S , et al . Binding of HIV-1 Nef to a novel thioesterase enzyme correlates with Nef-mediated CD4 down-regulation [J ] . The Journal of Biological Chemistry , 1997 , 272 ( 21 ): 13779 - 13785 .

PALMEIRA J D F , ARGAÑARAZ G A , DE OLIVEIRA G X L M , et al . Physiological relevance of ACOT8-Nef interaction in HIV infection [J ] . Reviews in Medical Virology , 2019 , 29 ( 5 ): e2057 .

STAUDT R P , ALVARADO J J , EMERT-SEDLAK L A , et al . Structure, function, and inhibitor targeting of HIV-1 Nef-effector kinase complexes [J ] . The Journal of Biological Chemistry , 2020 , 295 ( 44 ): 15158 - 15171 .

HOBSON C , CHAN A N , WRIGHT G D . The antibiotic resistome: a guide for the discovery of natural products as antimicrobial agents [J ] . Chemical Reviews , 2021 , 121 ( 6 ): 3464 - 3494 .

GAUDÊNCIO S P , PEREIRA F . Dereplication: racing to speed up the natural products discovery process [J ] . Natural Product Reports , 2015 , 32 ( 6 ): 779 - 810 .

COX G , SIERON A , KING A M , et al . A common platform for antibiotic dereplication and adjuvant discovery [J ] . Cell Chemical Biology , 2017 , 24 ( 1 ): 98 - 109 .

ZUBYK H L , COX G , WRIGHT G D . Antibiotic dereplication using the antibiotic resistance platform [J ] . Journal of Visualized Experiments , 2019 ( 152 ): e60536 .

TANG M C , ZOU Y , YEE D , et al . Identification of the pyranonigrin A biosynthetic gene cluster by genome mining in Penicillium thymicola IBT 5891 [J ] . AIChE Journal , 2018 , 64 ( 12 ): 4182 - 4186 .

TANG X Y , LI J , MILLÁN-AGUIÑAGA N , et al . Identification of thiotetronic acid antibiotic biosynthetic pathways by target-directed genome mining [J ] . ACS Chemical Biology , 2015 , 10 ( 12 ): 2841 - 2849 .

WHITE S W , ZHENG J , ZHANG Y M , et al . The structural biology of type Ⅱ fatty acid biosynthesis [J ] . Annual Review of Biochemistry , 2005 , 74 : 791 - 831 .

YAO J W , ROCK C O . How bacterial pathogens eat host lipids: implications for the development of fatty acid synthesis therapeutics [J ] . The Journal of Biological Chemistry , 2015 , 290 ( 10 ): 5940 - 5946 .

SASAKI H , OISHI H , HAYASHI T , et al . Thiolactomycin, a new antibiotic. Ⅱ. Structure elucidation [J ] . The Journal of Antibiotics , 1982 , 35 ( 4 ): 396 - 400 .

YEH H H , AHUJA M , CHIANG Y M , et al . Resistance gene-guided genome mining: serial promoter exchanges in Aspergillus nidulans reveal the biosynthetic pathway for fellutamide B, a proteasome inhibitor [J ] . ACS Chemical Biology , 2016 , 11 ( 8 ): 2275 - 2284 .

RODRIGUEZ-VILARIÑO S , ARRIBAS J , ARIZTI P , et al . Proteolytic processing and assembly of the C5 subunit into the proteasome complex [J ] . The Journal of Biological Chemistry , 2000 , 275 ( 9 ): 6592 - 6599 .

HINES J , GROLL M , FAHNESTOCK M , et al . Proteasome inhibition by fellutamide B induces nerve growth factor synthesis [J ] . Chemistry & Biology , 2008 , 15 ( 5 ): 501 - 512 .

BAUMANN S , HERRMANN J , RAJU R , et al . Cystobactamids: myxobacterial topoisomerase inhibitors exhibiting potent antibacterial activity [J ] . Angewandte Chemie International Edition , 2014 , 53 ( 52 ): 14605 - 14609 .

VETTING M W , HEGDE S S , ZHANG Y , et al . Pentapeptide-repeat proteins that act as topoisomerase poison resistance factors have a common dimer interface [J ] . Acta Crystallographica Section F, Structural Biology and Crystallization Communications , 2011 , 67 ( Pt 3 ): 296 - 302 .

PANTER F , KRUG D , BAUMANN S , et al . Self-resistance guided genome mining uncovers new topoisomerase inhibitors from myxobacteria [J ] . Chemical Science , 2018 , 9 ( 21 ): 4898 - 4908 .

YAN Y , LIU Q K , ZANG X , et al . Resistance-gene-directed discovery of a natural-product herbicide with a new mode of action [J ] . Nature , 2018 , 559 ( 7714 ): 415 - 418 .

AMORIM FRANCO T M , BLANCHARD J S . Bacterial branched-chain amino acid biosynthesis: structures, mechanisms, and drugability [J ] . Biochemistry , 2017 , 56 ( 44 ): 5849 - 5865 .

HALL C J , MACKIE E R R , GENDALL A R , et al . Review: amino acid biosynthesis as a target for herbicide development [J ] . Pest Management Science , 2020 , 76 ( 12 ): 3896 - 3904 .

FLINT D H , NUDELMAN A . Studies on the active site of dihydroxy-acid dehydratase [J ] . Bioorganic Chemistry , 1993 , 21 ( 4 ): 367 - 385 .

TSUDA Y , KANEDA M , TADA A , et al . Aspterric acid, a new sesquiterpenoid of the carotane group, a metabolite from Aspergillus terreus IFO-6123. X-Ray crystal and molecular structure of its p -bromobenzoate [J ] . Journal of the Chemical Society, Chemical Communications , 1978 ( 4 ): 160 .

ALANJARY M , KRONMILLER B , ADAMEK M , et al . The Antibiotic Resistant Target Seeker (ARTS), an exploration engine for antibiotic cluster prioritization and novel drug target discovery [J ] . Nucleic Acids Research , 2017 , 45 ( W1 ): W42 - W48 .

BLIN K , WOLF T , CHEVRETTE M G , et al . antiSMASH 4.0-improvements in chemistry prediction and gene cluster boundary identification [J ] . Nucleic Acids Research , 2017 , 45 ( W1 ): W36 - W41 .

WEBER T , BLIN K , DUDDELA S , et al . antiSMASH 3.0-a comprehensive resource for the genome mining of biosynthetic gene clusters [J ] . Nucleic Acids Research , 2015 , 43 ( W1 ): W237 - W243 .

MUNGAN M D , ALANJARY M , BLIN K , et al . ARTS 2.0: feature updates and expansion of the Antibiotic Resistant Target Seeker for comparative genome mining [J ] . Nucleic Acids Research , 2020 , 48 ( W1 ): W546 - W552 .

DE LOS SANTOS E L C , CHALLIS G L . clusterTools: proximity searches for functional elements to identify putative biosynthetic gene clusters [EB/OL ] . bioRxiv , 2017 , 119214 . ( 2017-12-12 )[ 2023-12-01 ] . https://www.biorxiv.org/content/10.1101/119214v2 https://www.biorxiv.org/content/10.1101/119214v2 .

EDDY S R . What is a hidden Markov model? [J ] . Nature Biotechnology , 2004 , 22 ( 10 ): 1315 - 1316 .

BRAUN V , PRAMANIK A , GWINNER T , et al . Sideromycins: tools and antibiotics [J ] . BioMetals 2009 , 22 ( 1 ): 3 - 13 .

ZENG Y , KULKARNI A , YANG Z Y , et al . Biosynthesis of albomycin δ 2 provides a template for assembling siderophore and aminoacyl-tRNA synthetase inhibitor conjugates [J ] . ACS Chemical Biology , 2012 , 7 ( 9 ): 1565 - 1575 .

GARG R P , QIAN X L , ALEMANY L B , et al . Investigations of valanimycin biosynthesis: elucidation of the role of seryl-tRNA [J ] . Proceedings of the National Academy of Sciences of the United States of America , 2008 , 105 ( 18 ): 6543 - 6547 .

STEFANSKA A L , CASSELS R , READY S J , et al . SB-203207 and SB-203208, two novel isoleucyl tRNA synthetase inhibitors from a Streptomyces sp. Ⅰ. Fermentation, isolation and properties [J ] . The Journal of Antibiotics , 2000 , 53 ( 4 ): 357 - 363 .

HU Z J , AWAKAWA T , MA Z J , et al . Aminoacyl sulfonamide assembly in SB-203208 biosynthesis [J ] . Nature Communications , 2019 , 10 ( 1 ): 184 .

THAKER M N , WANG W L , SPANOGIANNOPOULOS P , et al . Identifying producers of antibacterial compounds by screening for antibiotic resistance [J ] . Nature Biotechnology , 2013 , 31 ( 10 ): 922 - 927 .

CULP E J , WAGLECHNER N , WANG W L , et al . Evolution-guided discovery of antibiotics that inhibit peptidoglycan remodelling [J ] . Nature , 2020 , 578 ( 7796 ): 582 - 587 .

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