Harnessing in vivo synthesis of bioactive multiarylmethanes in Escherichia coli via oxygen-mediated free radical reaction induced by simple phenols.

Donglou Wang, Jiangbo He, Yonghong Chen, Boran Liu, Zhuang Wu, Xuerong Pan, Xuemei Niu
Author Information
  1. Donglou Wang: State Key Laboratory for Conservation and Utilization of Bio-Resources & Key Laboratory for Microbial Resources of the Ministry of Education, School of Life Sciences, Yunnan University, Kunming, 650091, P. R. China.
  2. Jiangbo He: Kunming Key Laboratory of Respiratory Disease, Kunming University, Kunming, 650214, P. R. China.
  3. Yonghong Chen: State Key Laboratory for Conservation and Utilization of Bio-Resources & Key Laboratory for Microbial Resources of the Ministry of Education, School of Life Sciences, Yunnan University, Kunming, 650091, P. R. China.
  4. Boran Liu: State Key Laboratory for Conservation and Utilization of Bio-Resources & Key Laboratory for Microbial Resources of the Ministry of Education, School of Life Sciences, Yunnan University, Kunming, 650091, P. R. China.
  5. Zhuang Wu: State Key Laboratory for Conservation and Utilization of Bio-Resources & Key Laboratory for Microbial Resources of the Ministry of Education, School of Life Sciences, Yunnan University, Kunming, 650091, P. R. China.
  6. Xuerong Pan: State Key Laboratory for Conservation and Utilization of Bio-Resources & Key Laboratory for Microbial Resources of the Ministry of Education, School of Life Sciences, Yunnan University, Kunming, 650091, P. R. China.
  7. Xuemei Niu: State Key Laboratory for Conservation and Utilization of Bio-Resources & Key Laboratory for Microbial Resources of the Ministry of Education, School of Life Sciences, Yunnan University, Kunming, 650091, P. R. China. xmniu@ynu.edu.cn. ORCID

Abstract

BACKGROUND: Xanthenes and multi-aryl carbon core containing compounds represent different types of complex and condensed architectures that have impressive wide range of pharmacological, industrial and synthetic applications. Moreover, indoles as building blocks were only found in naturally occurring metabolites with di-aryl carbon cores and in chemically synthesized tri-aryl carbon core containing compounds. Up to date, rare xanthenes with indole bearing multicaryl carbon core have been reported in natural or synthetic products. The underlying mechanism of fluorescein-like arthrocolins with tetra-arylmethyl core were synthesized in an engineered Escherichia coli fed with toluquinol remained unclear.
RESULTS: In this study, the Keio collection of single gene knockout strains of 3901 mutants of E. coli BW25113, together with 14 distinct E. coli strains, was applied to explore the origins of endogenous building blocks and the biogenesis for arthrocolin assemblage. Deficiency in bacterial respiratory and aromatic compound degradation genes ubiX, cydB, sucA and ssuE inhibited the mutant growth fed with toluquinol. Metabolomics of the cultures of 3897 mutants revealed that only disruption of tnaA involving in transforming tryptophan to indole, resulted in absence of arthrocolins. Further media optimization, thermal cell killing and cell free analysis indicated that a non-enzyme reaction was involved in the arthrocolin biosynthesis in E. coli. Evaluation of redox potentials and free radicals suggested that an oxygen-mediated free radical reaction was responsible for arthrocolins formation in E. coli. Regulation of oxygen combined with distinct phenol derivatives as inducer, 31 arylmethyl core containing metabolites including 13 new and 8 biological active, were isolated and characterized. Among them, novel arthrocolins with p-hydroxylbenzene ring from tyrosine were achieved through large scale of aerobic fermentation and elucidated x-ray diffraction analysis. Moreover, most of the known compounds in this study were for the first time synthesized in a microbe instead of chemical synthesis. Through feeding the rat with toluquinol after colonizing the intestines of rat with E. coli, arthrocolins also appeared in the rat blood.
CONCLUSION: Our findings provide a mechanistic insight into in vivo synthesis of complex and condensed arthrocolins induced by simple phenols and exploits a quinol based method to generate endogenous aromatic building blocks, as well as a methylidene unit, for the bacteria-facilitated synthesis of multiarylmethanes.

Keywords

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MeSH Term

Escherichia coli
Phenols
Oxygen
Free Radicals
Methane
Animals
Rats
Indoles

Chemicals

Phenols
Oxygen
Free Radicals
Methane
Indoles

Word Cloud

Created with Highcharts 10.0.0coliarthrocolinscoreEfreesynthesiscarbonreactioncontainingcompoundsbuildingblockssynthesizedEscherichiatoluquinolradicalratvivocomplexcondensedsyntheticMoreovermetabolitesindolefedstudystrainsmutantsdistinctendogenousarthrocolinaromaticcellanalysisoxygen-mediatedinducedsimplephenolsmultiarylmethanesBACKGROUND:Xanthenesmulti-arylrepresentdifferenttypesarchitecturesimpressivewiderangepharmacologicalindustrialapplicationsindolesfoundnaturallyoccurringdi-arylcoreschemicallytri-aryldaterarexanthenesbearingmulticarylreportednaturalproductsunderlyingmechanismfluorescein-liketetra-arylmethylengineeredremainedunclearRESULTS:Keiocollectionsinglegeneknockout3901BW25113together14appliedexploreoriginsbiogenesisassemblageDeficiencybacterialrespiratorycompounddegradationgenesubiXcydBsucAssuEinhibitedmutantgrowthMetabolomicscultures3897revealeddisruptiontnaAinvolvingtransformingtryptophanresultedabsencemediaoptimizationthermalkillingindicatednon-enzymeinvolvedbiosynthesisEvaluationredoxpotentialsradicalssuggestedresponsibleformationRegulationoxygencombinedphenolderivativesinducer31arylmethylincluding13new8biologicalactiveisolatedcharacterizedAmongnovelp-hydroxylbenzeneringtyrosineachievedlargescaleaerobicfermentationelucidatedx-raydiffractionknownfirsttimemicrobeinsteadchemicalfeedingcolonizingintestinesalsoappearedbloodCONCLUSION:findingsprovidemechanisticinsightexploitsquinolbasedmethodgeneratewellmethylideneunitbacteria-facilitatedHarnessingbioactiveviaAntitumorArthrocolinsMultiarylmethanesOxygen-mediated

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