{"title":"Metabolic engineering in Hot Acid: Strategies enabling chemolithotrophy in thermoacidophilic archaea","authors":"Daniel J. Willard , Robert M. Kelly","doi":"10.1016/j.ymben.2025.06.005","DOIUrl":null,"url":null,"abstract":"<div><div>A genome-scale metabolic model was developed to explore metabolic engineering strategies for thermoacidophilic archaea, with a focus on the genetically tractable <em>Sulfolobus acidocaldarius</em> (T<sub>opt</sub> 75 °C, pH<sub>opt</sub> 2.5). <em>S. acidocaldarius</em> is natively neither an autotroph nor a sulfur oxidizer, although its genome suggests that this might have been the case at some evolutionary point. Comparative genomics provided insights into key genes and pathways missing from <em>S. acidocaldarius</em> necessary for chemolithotrophy. Growth data for the chemolithotrophic sulfur oxidizer, <em>Sulfurisphaera ohwakuensis</em> (T<sub>opt</sub> 85 °C, pH<sub>opt</sub> 2.0), provided metabolic data to inform model development. Previous metabolic engineering efforts enabled sulfur oxidation by <em>S. acidocaldarius</em>, albeit at levels below native sulfur oxidizers. Model analysis pointed to active sulfur transport as a key missing complement to passive diffusion. Modelling results predicted that sulfur oxidation could drive production of a bio-based chemical, acetone, in engineered strains of <em>S. acidocaldarius</em> with concomitant fixation of CO<sub>2</sub> into product via the 3-Hydroxybutyrate/4-Hydroxybutyrate cycle. The findings here provide new insights into the basis for thermoacidophile chemolithotrophy and motivate further efforts to develop <em>S. acidocaldarius</em> into a valuable metabolic engineering platform.</div></div>","PeriodicalId":18483,"journal":{"name":"Metabolic engineering","volume":"91 ","pages":"Pages 366-378"},"PeriodicalIF":6.8000,"publicationDate":"2025-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Metabolic engineering","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1096717625000916","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
A genome-scale metabolic model was developed to explore metabolic engineering strategies for thermoacidophilic archaea, with a focus on the genetically tractable Sulfolobus acidocaldarius (Topt 75 °C, pHopt 2.5). S. acidocaldarius is natively neither an autotroph nor a sulfur oxidizer, although its genome suggests that this might have been the case at some evolutionary point. Comparative genomics provided insights into key genes and pathways missing from S. acidocaldarius necessary for chemolithotrophy. Growth data for the chemolithotrophic sulfur oxidizer, Sulfurisphaera ohwakuensis (Topt 85 °C, pHopt 2.0), provided metabolic data to inform model development. Previous metabolic engineering efforts enabled sulfur oxidation by S. acidocaldarius, albeit at levels below native sulfur oxidizers. Model analysis pointed to active sulfur transport as a key missing complement to passive diffusion. Modelling results predicted that sulfur oxidation could drive production of a bio-based chemical, acetone, in engineered strains of S. acidocaldarius with concomitant fixation of CO2 into product via the 3-Hydroxybutyrate/4-Hydroxybutyrate cycle. The findings here provide new insights into the basis for thermoacidophile chemolithotrophy and motivate further efforts to develop S. acidocaldarius into a valuable metabolic engineering platform.
期刊介绍:
Metabolic Engineering (MBE) is a journal that focuses on publishing original research papers on the directed modulation of metabolic pathways for metabolite overproduction or the enhancement of cellular properties. It welcomes papers that describe the engineering of native pathways and the synthesis of heterologous pathways to convert microorganisms into microbial cell factories. The journal covers experimental, computational, and modeling approaches for understanding metabolic pathways and manipulating them through genetic, media, or environmental means. Effective exploration of metabolic pathways necessitates the use of molecular biology and biochemistry methods, as well as engineering techniques for modeling and data analysis. MBE serves as a platform for interdisciplinary research in fields such as biochemistry, molecular biology, applied microbiology, cellular physiology, cellular nutrition in health and disease, and biochemical engineering. The journal publishes various types of papers, including original research papers and review papers. It is indexed and abstracted in databases such as Scopus, Embase, EMBiology, Current Contents - Life Sciences and Clinical Medicine, Science Citation Index, PubMed/Medline, CAS and Biotechnology Citation Index.