The printer would like to correct an error in the article “Loss of Function of KRE5 Suppresses Temperature Sensitivity of Mutants Lacking Mitochondrial Anionic Lipids” (Mol. Biol. Cell [2005] 16, 665–675). All instances of “[ρ]” should have been removed from the column titled “Medium” in Table 2. The correct Table 2 is published below:

Table 2.

Cell wall composition in pgs1Δ and suppressor mutants

		Alkaline-insoluble glucan			Alkaline-soluble
Strain	Medium	β-1,6	β-1,6 + β-1,3	β-1,3	β-1,3-glucan	Chitin
WT	YPD	37.8 ± 0.9	141.4 ± 4.4	103.6	100%	4.65 ± 0.39
WT ρ0	YPD	23.7 ± 1.4	114.7 ± 8.1	91.0	50 ± 3%	4.54 ± 0.26
pgs1Δ ρ0	YPD	12.1 ± 1.9	74.7 ± 1.4	62.6	38 ± 2%	12.36 ± 1.67
pgs1Δ kre5W1166X ρ0	YPD	7.7 ± 2.5	155.8 ± 1.4	148.1	174 ± 15%	12.35 ± 0.39
pgs1Δ ρ0	YPDS	21.0 ± 1.6	98.8 ± 18.8	77.8	90 ± 25%	8.09 ± 1.52
pgs1Δ ρ0 + PGS1	Ura-	25.8 ± 5.3	131.6 ± 33.5	105.8	100%	7.76 ± 0.32
pgs1Δ ρ0 + vec	Ura-	21.4 ± 2.1	69.6 ± 22.7	48.2	41 ± 6%	12.04 ± 0.80
pgs1Δ kre5W1166X ρ0 + vec	Ura-	7.4 ± 1.8	118.4 ± 17.3	111.0	151 ± 21%	12.09 ± 3.14
pgs1Δ kre5W1166X ρ0 + KRE5	Ura-	27.1 ± 0.9	99.3 ± 9.6	72.2	52 ± 5%	10.52 ± 0.37

Glucan and chitin levels were measured as described in Materials and Methods in wild-type (FGY3), ρ⁰, pgs1Δ (QZY24B), and suppressor mutant pgs1Δ kre5^W1166X (QZY11A) cells grown in YPD or YPDS; pgs1Δ (QZY24B) cells transformed with empty vector pYES2/CT (+vec) or pYES2/CT-PGS1 (+PGS1); and pgs1Δ kre5^W1166X suppressor mutant (QZY11A) cells transformed with empty vector YCp50 (+vec) or the genomic clone of KRE5 (+KRE5) grown in synthetic ura^- medium. Alkaline insoluble glucan and chitin are expressed as micrograms per milligram of cell dry weight. Alkaline soluble β-1,3-glucan in cells grown in complex medium (top) was expressed as a percentage of that of wild-type (FGY3) cells. Alkaline soluble β-1,3-glucan in cells grown in synthetic ura^- medium (bottom) was expressed relative to pgs1Δ (QZY24B) cells transformed with pYES2/CT-PGS1. Data represent three independent experiments.