Lee L S, Garnett H M
Queensland Department of Primary Industries, Bundaberg Research Station, Australia.
J Biochem Biophys Methods. 1993 Jul;26(4):249-60. doi: 10.1016/0165-022x(93)90026-k.
A method of estimating total double-stranded DNA in crude extracts of citrus leaf tissue by evaluating the enhancement of fluorescence intensity of 4',6-diamidino-2-phenylindole (DAPI) was assessed. For pure citrus DNA and citrus leaf tissue crude extract each in the presence of 100 ng/ml DAPI, excitation spectral response curves converged at excitation wavelength of 360 nm. At this excitation wavelength, maximum fluorescence intensity occurred across a range of emission wavelengths from 445 nm to 460 nm. The appropriate excitation and emission wavelengths were shown to be 360 nm and 450 nm, respectively. Fluorescence intensity increased linearly with DNA concentration and non-DNA components of the tissue homogenates had negligible effect on fluorescence at these wavelengths. Sodium dodecyl sulfate (SDS) in the incubation solution resulted in some suppression of DAPI-DNA fluorescence and produced a non-linear response to changing DNA concentration. The method should be applicable to DNA quantitation from crude tissue extracts of any plant species.
评估了一种通过评估4',6-二脒基-2-苯基吲哚(DAPI)荧光强度增强来估算柑橘叶组织粗提物中双链DNA总量的方法。对于纯柑橘DNA和分别存在100 ng/ml DAPI的柑橘叶组织粗提物,激发光谱响应曲线在360 nm激发波长处收敛。在此激发波长下,在445 nm至460 nm的发射波长范围内出现最大荧光强度。结果表明,合适的激发和发射波长分别为360 nm和450 nm。荧光强度随DNA浓度呈线性增加,并且组织匀浆中的非DNA成分在这些波长下对荧光的影响可忽略不计。孵育溶液中的十二烷基硫酸钠(SDS)导致DAPI-DNA荧光有一定程度的抑制,并对变化的DNA浓度产生非线性响应。该方法应适用于任何植物物种粗组织提取物的DNA定量。