Table 1 SMT analysis data for RarA-mVenus in recombination and Y-polymerases defective backgrounds.

From: Single molecule tracking reveals functions for RarA at replication forks but also independently from replication during DNA repair in Bacillus subtilis

Background

D (μm2 s−1)

−drug

+H2O2

+MMC

static

dyna

static

dyn

static

dyn

static

dyn

Wild type

0.23

2.3

48

52

35

65

44

56

∆recO

0.39

2.3

61

39

47

53

57

43

recF15

0.2

2.1

42

58

51

49

48

52

∆recD2

0.26

2.2

63

37

50

50

36

64

∆recX

0.26

2.4

54

46

40

60

46

54

∆addAB

0.24

2.2

55

45

55

45

76

24

∆recJ

0.21

2.3

59

41

61

39

64

36

∆recQ

0.19

2.2

43

57

48

52

43

57

∆recS

0.28

2.6

71

29

50

50

56

44

∆recU

0.37

2.1

42

58

57

43

65

35

∆recG

0.21

2

46

54

43

57

55

45

∆ruvAB

0.26

2.7

63

37

44

56

59

41

∆radA/sms

0.28

2.9

57

43

57

43

58

42

∆polY1

0.3

2.5

52

48

33

67

34

66

∆polY2

0.28

2.1

47

53

38

62

48

52

DnaX-CFP

0.28

2.2

53

47

41

59

49

51

  1. adyn; dynamic. Apparent diffusion coefficients (in μm2 s−1) and static/dynamic population weights (in %) calculated by step-size distributions and Gaussian fits for RarA-mVenus in the different backgrounds studied in exponential growth, and after 60 min induction with 0.5 mM H2O2 or 50 ng/ml MMC. Cells were grown at 25 °C and images were taken at room temperature. At least 200 tracks/condition were considered for the analysis.