Gene_locus Report for: 9chlr-7QJM202

Chloroflexus sp. MS-G alpha/beta fold hydrolase Xaa-Pro-like_dom

202 YNPsite05_CeleraDRAFT_401410 Environmental sample 7QJM only c-term ; 176767 pEE010 202; 176779 pEE022 214 YNPsite06_CeleraDRAFT_160970 Environmental sample

(Below N is a link to NCBI taxonomic web page and E link to ESTHER at designed phylum.)
> cellular organisms: N E > Bacteria: N E > Terrabacteria group: N E > Chloroflexi: N E > Chloroflexia: N E > Chloroflexales: N E > Chloroflexineae: N E > Chloroflexaceae: N E > Chloroflexus: N E > unclassified Chloroflexus: N E > Chloroflexus sp. MS-G: N E

Title: Sourcing thermotolerant poly(ethylene terephthalate) hydrolase scaffolds from natural diversity
Erickson E, Gado JE, Avilan L, Bratti F, Brizendine RK, Cox PA, Gill R, Graham R, Kim DJ and McGeehan JE <11 more author(s)> Erickson E, Gado JE, Avilan L, Bratti F, Brizendine RK, Cox PA, Gill R, Graham R, Kim DJ, Konig G, Michener WE, Poudel S, Ramirez KJ, Shakespeare TJ, Zahn M, Boyd ES, Payne CM, Dubois JL, Pickford AR, Beckham GT, McGeehan JE (- 11)
Ref: Nat Commun, 13:7850, 2022 : PubMed
Abstract


ESTHER: Erickson_2022_Nat.Commun_13_7850
PubMedSearch: Erickson 2022 Nat.Commun 13 7850
PubMedID: 36543766
Gene_locus related to this paper: 9arch-PETcan211, 9cren-PETcan204, 9cyan-305pEE028, 9bact-102Pee006, 9chlr-7QJM202, 9bact-a0a656d8b6, 9actn-a0a1t4kk94, 9burk-PET11, 9bact-c3ryl0, thecs-711Erick, 9actn-RII04304, 9actn-h6wx58, thecd-d1a9g5, thecd-d1a2h1, 9acto-d4q9n1, 9acto-f7ix06, 9gamm-a0a3l8bw54, 9actn-a0a0n0my27, 9burk-a0a1e4lw26, 9actn-Alr407, 9gamm-a0a3l8bdt3, 9gamm-a0a2k9lit3, 9bact-g9by57, bacsu-pnbae, thefu-q6a0i4, 9actn-a0a0n0ney5, 9pseu-a0a1i6nu60, thefu-q6a0i3, 9actn-a0a147kjy8, 9actn-e9upm2

Abstract

Enzymatic deconstruction of poly(ethylene terephthalate) (PET) is under intense investigation, given the ability of hydrolase enzymes to depolymerize PET to its constituent monomers near the polymer glass transition temperature. To date, reported PET hydrolases have been sourced from a relatively narrow sequence space. Here, we identify additional PET-active biocatalysts from natural diversity by using bioinformatics and machine learning to mine 74 putative thermotolerant PET hydrolases. We successfully express, purify, and assay 51 enzymes from seven distinct phylogenetic groups; observing PET hydrolysis activity on amorphous PET film from 37 enzymes in reactions spanning pH from 4.5-9.0 and temperatures from 30-70 degreesC. We conduct PET hydrolysis time-course reactions with the best-performing enzymes, where we observe differences in substrate selectivity as function of PET morphology. We employed X-ray crystallography and AlphaFold to examine the enzyme architectures of all 74 candidates, revealing protein folds and accessory domains not previously associated with PET deconstruction. Overall, this study expands the number and diversity of thermotolerant scaffolds for enzymatic PET deconstruction.