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. 1999 Jul;181(14):4205–4215. doi: 10.1128/jb.181.14.4205-4215.1999

TABLE 2.

Photopigment synthesis and photosynthetic gene expression in reg mutants of Rhodobacter capsulatus complemented with reg genes from various species

Strain BChl content (nmol/mg)c
Expression of puf operond
−O2 +O2 −O2 +O2
Wild type (R. capsulatus) 34.5 0.5 544 ± 30 15 ± 5
TB2(pJRD215)a vector only 13.9 0.3 40 ± 10 9 ± 5
TB2(pMWS3.1) +Rhodobacter regA-senC 37.2 0.7 382 ± 50 62 ± 20
TB2(pMCS003) +Rhodovulum regA-senC 51.5 0.6 1,971 ± 150 125 ± 25
TB2(pMCR001) +Roseobacter regA-senC 42.5 0.6 315 ± 30 60 ± 15
SD01(pJRD215)b vector only 21.6 0.5 135 ± 70 18 ± 10
SD01(pCSM9e) +Rhodobacter regB-senC 42.8 0.5 1,050 ± 145 108 ± 40
SD01(pMCS010) +Rhodovulum regB 45.7 0.5 855 ± 150 60 ± 20
SD01(pMCR010) +Roseobacter regB-senC 40.1 0.4 499 ± 125 63 ± 25
a

TB2; R. capsulatusregA). 

b

SD01; R. capsulatusregB). 

c

BChl content in membranes (nanomoles per milligram of membrane protein). Data are based on the average of three independent assays. Uncertainty limits in this assay are within 5% in all transconjugants and the wild type. −O2, anaerobic photosynthetic growth; +O2, aerobic-dark growth. 

d

Values are β-galactosidase activity (micromoles of o-nitrophenol-β-d-galactoside hydrolyzed per minute per milligram of protein) of strains with the puf::lacZ translational fusion in pCB532Ω (4).