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. 2011 Nov 11;6(11):e27302. doi: 10.1371/journal.pone.0027302

Table 2. The effect of maltose on MICAmp and protein expression.

MICAmp (µg/ml)b Accumulationc
Proteina − Maltose + Maltose Ratiod Ratiod Stdeve
Nonef 1 1 1 2.4 0.2
MBP 1 1 1 1.0 0.1
BLA 8192 8192 1 1.3 0.1
MBP317-347 16–32 512 16–32 31.3 4.5
Ph1 32 512–1024 32–64 14.6 3.1
Ph3 256 1024–2048 4–8 10.7 1.0
Ph5 16–32 256–512 8–32 17.6 5.9
Ph7 32–64 1024 16–32 25.7 6.5
Ph8 32 512–1024 16–32 19.2 7.5
Ph12 64 1024–2048 16–32 38.9 10.1
Ph14 128 2048 16 12.4 6.8
Ph16 1024 4096 4 5.4 2.1
Ph17 32 1024 32 49.2 7.9
Ph19 256 2048 8 14.7 2.2
Ph24 4–8 128 32 21.5 4.7
Ph27 256 2048 8 11.1 3.7
Ph28 64 1024–2048 16–32 22.7 7.2
c4 1024–2048 2048 1–2 5.3 5.0
a

Protein expressed from plasmid pDIMC8 in RH22 cells.

b

MICAmp was determined in triplicate. For proteins with a MICAmp range, this indicates the range from the three experiments (e.g. Ph5 was found to have a MICAmp in the absence of maltose of 16 µg/ml in some trials and 32 µg/ml in other trials).

c

Accumulation ratio determined from quantitative image analysis of western blots probed using polyclonal anti-BLA antibodies (except for MBP which was probed with anti-MBP antibodies).

d

(With maltose)/(without maltose).

e

Standard deviation calculated from three independent experiments.

f

No pDIMC8 plasmid was present. The protein monitored by western blot was chromosomally encoded MBP.