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. 2007 Jan;175(1):41–54. doi: 10.1534/genetics.106.065524

TABLE 1.

rec and related mutations used in this study

Allele Description Source or reference
recB21∷IS186 IS186 insertion at codon 305 Schultz et al. (1983); Amundsen et al. (2000)
recC73 ΔT at codon 646 Schultz et al. (1983); Arnold et al. (2000)
recC1041 Trp841 → UGA841 Amundsen et al. (2002)
recC1010 Gly905 → Glu905 Chaudhury and Smith (1984b); Amundsen et al. (2002)
recC2710–C2718 ExoIII-generated deletions (see Figure 3) Amundsen et al. (2002)
recC2725 UGA841 UGA842 plus C-terminal deletiona This study
recC2726 UGA841 UAA842 plus C-terminal deletionb This study
ΔrecC2730kan Substitution of kan for recC ORF This study
recD1013 Gln4 → UAA4 Chaudhury and Smith (1984b); Amundsen et al. (1986, 2002)
ΔrecBCD232 thyA–recBCD–argA deletion Chaudhury and Smith (1984a)
ΔrecBCD234 recC–argA deletionc Chaudhury and Smith (1984a)
ΔrecAkan Substitution of kan for recA ORF Reddy and Gowrishankar (2000)
recJ284∷Tn10 Tn10 insertion Lovett and Clark (1984)
ΔxonA∷FRTkanFRT Substitution of kan for xonA ORF Feschenko et al. (2003)
sbcB15 Ala183 → Tyr183 GenBank accession AM235176
a

The deletion leaves codons 1–840 intact.

b

The deletion leaves codons 1–840 intact. An additional 6 bp specifying the KpnI recognition site (5′-GGTACC-3′) are 3′ of UAA842.

c

The deletion ends between codons 605 and 630 of recC (Figure 3; Amundsen et al. 2002).