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. 1997 Dec 9;94(25):14150–14155. doi: 10.1073/pnas.94.25.14150

Table 4.

Capacity of E. coli-expressed R. communis phloem sap proteins to move from cell to cell when microinjected into mesophyll cells within the cotyledons of C. maxima plants

Injected material Protein concentration, mg⋅ml−1 Micro- injections* Extent of movement
LYCH 18 (18; 100%) 20–30 cells
20-kDa FD 0 (18; 0%) 0 cells
FITC-glutaredoxin 5.0 10 (17; 59%) 10–12 cells
Glutaredoxin + 20-kDa FD 2.5 6 (12; 50%) 10–12 cells
Glutaredoxin + 40-kDa FD 2.5 1 (12; 8%) 4 cells
FITC-cystatin 2.3 5 (11; 45%) 10–12 cells
Cystatin + 20-kDa FD 1.7 6 (12; 50%) 10–12 cells
Cystatin + 40-kDa FD 1.7 1 (10; 10%) 3 cells
Ubiquitin + 20-kDa FD 1.0 1 (10; 10%) 3 cells
FITC-ubiquitin§ 3.0 0 (16; 0%) 0 cells
FITC-ΔC-ubiquitin§ 3.0 2 (12; 16%) 3–4 cells
FITC-ΔC-ubiquitin§ + PP2 2.0 + 2.0 0 (8; 0%) 0 cells
FITC-ΔC-ubiquitin§ + KN1 2.0 + 2.0 1 (10; 10%) 3 cells

FD, FITC-dextran. 

*

Details as in Table 1

When movement of fluorescence was detected, it was confined to adjacent cells. 

Ubiquitin extracted from the phloem sap of R. communis. 

§

E. coli-expressed A. thaliana ubiquitin (wild-type) and ΔC-ubiquitin (C-terminal deletion mutant).