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. Author manuscript; available in PMC: 2023 Mar 1.
Published in final edited form as: Plant J. 2021 Dec 27;109(6):1441–1456. doi: 10.1111/tpj.15640

Table 1. Expression and secretion of individual GAUTs in HEK293 cells.

The number after the Δ represents the amino acid residue truncation site at which each GAUT construct was truncated to remove its putative TMD or to provide the in vivo cleavage site (GAUT1) prior to insertion into the pGEn2-DEST vector for expression in HEK293 cells. Synthesis in the cells and secretion into the medium of each GAUT protein was monitored by fluorescence of the N-terminal domain GFP tag. Values are total gross fluorescence units and represent the average ± SEM of the designated GAUT protein expression from at least two independent 20 mL HEK293 cell cultures.

GAUT Cells & Medium Fluorescence Medium Fluorescence
1Δ42 379 ± 144 105 ± 2
1Δ167 639 ± 34 366 ± 31
3Δ28 164 ± 9 69 ± 3
4Δ29 27 ± 5 18 ± 1
5Δ31 129 ± 42 50 ± 11
6Δ31 32 ± 2 19 ± 0
7Δ43 204 ± 60 59 ± 20
8Δ43 30 ± 5 19 ± 0
9Δ50 242 ± 112 35 ± 8
10Δ39 953 ± 111 372 ± 3
11Δ39 1128 ± 187 795 ± 82
12Δ59 302 ± 100 46 ± 6
13Δ61 718 ± 52 245 ± 23
14Δ61 715 ± 67 296 ± 30
15Δ70 380 ± 47 35 ± 3

These constructs were selected for purification from the HEK293 medium