4.7 Article

Functional analysis of GT61 glycosyltransferases from grass species in xylan substitutions

期刊

PLANTA
卷 254, 期 6, 页码 -

出版社

SPRINGER
DOI: 10.1007/s00425-021-03794-y

关键词

Arabinosyltransferase; Cell wall; Xylan; XAT; XYXT

资金

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-FG02-03ER15415]
  2. UGA Plant Biology Undergraduate Research Award

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Multiple members of the rice GT61 family were identified as xylan arabinosyltransferases (XATs) involved in 3-O-arabinosylation of xylan in grass species. Additionally, homologs of XATs and xylan 2-O-xylosyltransferases (XYXTs) in maize, sorghum, Brachypodium, and switchgrass were also found to exhibit similar activities, indicating evolutionary conservation of these functions in grass species.
Main conclusion Multiple rice GT61 members were demonstrated to be xylan arabinosyltransferases (XATs) mediating 3-O-arabinosylation of xylan and the functions of XATs and xylan 2-O-xylosyltransferases were shown to be conserved in grass species. Xylan is the major hemicellulose in the cell walls of grass species and it is typified by having arabinofuranosyl (Araf) substitutions. In this report, we demonstrated that four previously uncharacterized, Golgi-localized glycosyltransferases residing in clade A or B of the rice GT61 family were able to mediate 3-O-arabinosylation of xylan when heterologously expressed in the Arabidopsis gux1/2/3 triple mutant. Biochemical characterization of their recombinant proteins established that they were xylan arabinosyltransferases (XATs) capable of transferring Araf residues onto xylohexaose acceptors, and thus they were named OsXAT4, OsXAT5, OsXAT6 and OsXAT7. OsXAT5 and the previously identified OsXAT2 were shown to be able to arabinosylate xylooligomers with a degree of polymerization of as low as 3. Furthermore, a number of XAT homologs from maize, sorghum, Brachypodium and switchgrass were found to exhibit activities catalyzing Araf transfer onto xylohexaose, indicating that they are XATs involved in xylan arabinosylation in these grass species. Moreover, we revealed that homologs of another GT61 member, xylan 2-O-xylosyltransferase (XYXT1), from these grass species could mediate 2-O-xylosylation of xylan when expressed in the Arabidopsis gux1/2/3 mutant. Together, our findings indicate that multiple OsXATs are involved in 3-O-arabinosylation of xylan and the functions of XATs and XYXTs are conserved in grass species.

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