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  1. Article ; Online: Arabidopsis GELP7 functions as a plasma membrane-localized acetyl xylan esterase, and its overexpression improves saccharification efficiency.

    Rastogi, Lavi / Chaudhari, Aniket Anant / Sharma, Raunak / Pawar, Prashant Anupama-Mohan

    Plant molecular biology

    2022  Volume 109, Issue 6, Page(s) 781–797

    Abstract: Acetyl substitution on the xylan chain is critical for stable interaction with cellulose and other cell wall polymers in the secondary cell wall. Xylan acetylation pattern is governed by Golgi and extracellular localized acetyl xylan esterase (AXE). We ... ...

    Abstract Acetyl substitution on the xylan chain is critical for stable interaction with cellulose and other cell wall polymers in the secondary cell wall. Xylan acetylation pattern is governed by Golgi and extracellular localized acetyl xylan esterase (AXE). We investigated the role of Arabidopsis clade Id from the GDSL esterase/lipase or GELP family in polysaccharide deacetylation. The investigation of the AtGELP7 T-DNA mutant line showed a decrease in stem esterase activity and an increase in stem acetyl content. We further generated overexpressor AtGELP7 transgenic lines, and these lines showed an increase in AXE activity and a decrease in xylan acetylation compared to wild-type plants. Therefore, we have named this enzyme as AtAXE1. The subcellular localization and immunoblot studies showed that the AtAXE1 enzyme is secreted out, associated with the plasma membrane and involved in xylan de-esterification post-synthesis. The cellulose digestibility was improved in AtAXE1 overexpressor lines without pre-treatment, after alkali and xylanases pre-treatment. Furthermore, we have also established that the AtGELP7 gene is upregulated in the overexpressor line of AtMYB46, a secondary cell wall specific transcription factor. This transcriptional regulation can drive AtGELP7 or AtAXE1 to perform de-esterification of xylan in a tissue-specific manner. Overall, these data suggest that AtGELP7 overexpression in Arabidopsis reduces xylan acetylation and improves digestibility properties of polysaccharides of stem lignocellulosic biomass.
    MeSH term(s) Acetylesterase ; Arabidopsis/genetics ; Arabidopsis/metabolism ; Cell Membrane/metabolism ; Cell Wall/metabolism ; Cellulose/metabolism ; Esterases/genetics ; Polysaccharides/metabolism ; Xylans/metabolism
    Chemical Substances Polysaccharides ; Xylans ; Cellulose (9004-34-6) ; Esterases (EC 3.1.-) ; Acetylesterase (EC 3.1.1.6) ; acetylxylan esterase (EC 3.1.1.72)
    Language English
    Publishing date 2022-05-17
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 778032-1
    ISSN 1573-5028 ; 0167-4412
    ISSN (online) 1573-5028
    ISSN 0167-4412
    DOI 10.1007/s11103-022-01275-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Arabidopsis GELP7 functions as a plasma membrane-localized acetyl xylan esterase, and its overexpression improves saccharification efficiency

    Rastogi, Lavi / Chaudhari, Aniket Anant / Sharma, Raunak / Pawar, Prashant Anupama-Mohan

    Plant molecular biology. 2022 Aug., v. 109, no. 6

    2022  

    Abstract: Acetyl substitution on the xylan chain is critical for stable interaction with cellulose and other cell wall polymers in the secondary cell wall. Xylan acetylation pattern is governed by Golgi and extracellular localized acetyl xylan esterase (AXE). We ... ...

    Abstract Acetyl substitution on the xylan chain is critical for stable interaction with cellulose and other cell wall polymers in the secondary cell wall. Xylan acetylation pattern is governed by Golgi and extracellular localized acetyl xylan esterase (AXE). We investigated the role of Arabidopsis clade Id from the GDSL esterase/lipase or GELP family in polysaccharide deacetylation. The investigation of the AtGELP7 T-DNA mutant line showed a decrease in stem esterase activity and an increase in stem acetyl content. We further generated overexpressor AtGELP7 transgenic lines, and these lines showed an increase in AXE activity and a decrease in xylan acetylation compared to wild-type plants. Therefore, we have named this enzyme as AtAXE1. The subcellular localization and immunoblot studies showed that the AtAXE1 enzyme is secreted out, associated with the plasma membrane and involved in xylan de-esterification post-synthesis. The cellulose digestibility was improved in AtAXE1 overexpressor lines without pre-treatment, after alkali and xylanases pre-treatment. Furthermore, we have also established that the AtGELP7 gene is upregulated in the overexpressor line of AtMYB46, a secondary cell wall specific transcription factor. This transcriptional regulation can drive AtGELP7 or AtAXE1 to perform de-esterification of xylan in a tissue-specific manner. Overall, these data suggest that AtGELP7 overexpression in Arabidopsis reduces xylan acetylation and improves digestibility properties of polysaccharides of stem lignocellulosic biomass.
    Keywords Arabidopsis ; acetylation ; biomass ; carboxylic ester hydrolases ; cell walls ; cellulose ; digestibility ; genes ; genetically modified organisms ; lignocellulose ; molecular biology ; mutants ; plasma membrane ; saccharification ; transcription (genetics) ; transcription factors ; xylan ; xylanases
    Language English
    Dates of publication 2022-08
    Size p. 781-797.
    Publishing place Springer Netherlands
    Document type Article
    ZDB-ID 778032-1
    ISSN 1573-5028 ; 0167-4412
    ISSN (online) 1573-5028
    ISSN 0167-4412
    DOI 10.1007/s11103-022-01275-8
    Database NAL-Catalogue (AGRICOLA)

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