Lorenti A S, Viale A A
Rev Argent Microbiol. 1980 Sep-Dec;12(3):105-9.
The activity of aminolevulinate-synthetase in crude extracts of R. vannielii was determined. Its properties are very similar to those of the enzyme from R. palustris. With increasing light intensity on cultures of both microorganisms, their specific growth rates increases and the concentration of bacteriochlorophyll decreases. ALA-synthetase exhibits a dual-pattern; its activity remains at a high constant level up to 4 x 10(4) erg cm-2 seg-1, decreasing at higher light intensities (Figures 1 and 2). The activity of succinil-CoA-synthetase of both microorganisms and ALA-dehydrase of R. palustris remain constant over the entire range of light intensities used, but the ALA-dehydrase of R. vannielii shows the same dual-pattern as ALA-synthetase (Table 1), namely a constant high level at the lower light intensities, decreasing at the higher ones. With dialysis the activity of ALA-synthetase of both microorganisms decreases only in extracts from low light intensity grown bacteria, while it did not decrease in extracts from bacteria grown at high light intensities.
测定了凡氏红假单胞菌粗提物中氨基乙酰丙酸合成酶的活性。其性质与沼泽红假单胞菌的该酶非常相似。随着两种微生物培养物光照强度的增加,它们的比生长速率增加,细菌叶绿素浓度降低。氨基乙酰丙酸合成酶呈现出双重模式;在高达4×10⁴尔格·厘米⁻²·秒⁻¹的光照强度下,其活性保持在较高的恒定水平,在更高光照强度下则降低(图1和图2)。两种微生物的琥珀酰辅酶A合成酶活性以及沼泽红假单胞菌的氨基乙酰丙酸脱水酶活性在所用的整个光照强度范围内保持恒定,但凡氏红假单胞菌的氨基乙酰丙酸脱水酶与氨基乙酰丙酸合成酶表现出相同的双重模式(表1),即在较低光照强度下保持恒定的高水平,在较高光照强度下降低。通过透析,两种微生物的氨基乙酰丙酸合成酶活性仅在低光照强度下生长的细菌提取物中降低,而在高光照强度下生长的细菌提取物中则不降低。