Marie D, Vaulot D, Partensky F
Centre National de la Recherche Scientifique, Roscoff, France.
Appl Environ Microbiol. 1996 May;62(5):1649-55. doi: 10.1128/aem.62.5.1649-1655.1996.
Novel blue light-excited fluorescent dyes for nucleic acids (YOYO-1, YO-PRO-1, and PicoGreen) were tested on cultures of Escherichia coli and of a variety of marine prokaryotes. Results of flow cytometric DNA analyses were compared with those obtained with the UV-excited dyes bis-benzimide Hoechst 33342 or 4', 6-diamidino-2-phenylindole (DAPI). YOYO-1, YO-PRO-1, and PicoGreen can be used only on aldehyde-fixed cells and need to be supplemented with cofactors such as potassium, citrate, or EDTA. They are highly sensitive to ionic strength. Consequently, seawater culture samples cannot be stained directly with these dyes and require at least a 10-fold dilution with distilled water to obtain reliable fluorescence signals. After treatment with RNase, coefficients of variation for the G1 peak of the DNA distributions of the different strains tested with YOYO-1 or PicoGreen indicated in general an improvement over Hoechst 33342 staining. These novel dyes can be used to enumerate prokaryotic cells by flow cytometry, as demonstrated with E. coli. However, their sensitivity to ionic strength makes them unsuitable for cell cycle analysis in natural samples.
新型蓝光激发的核酸荧光染料(YOYO-1、YO-PRO-1和PicoGreen)在大肠杆菌和多种海洋原核生物培养物上进行了测试。流式细胞术DNA分析结果与用紫外线激发染料双苯甲酰亚胺Hoechst 33342或4',6-二脒基-2-苯基吲哚(DAPI)获得的结果进行了比较。YOYO-1、YO-PRO-1和PicoGreen仅可用于醛固定细胞,并且需要补充钾、柠檬酸盐或乙二胺四乙酸等辅助因子。它们对离子强度高度敏感。因此,海水培养样品不能直接用这些染料染色,需要用蒸馏水至少稀释10倍才能获得可靠的荧光信号。在用核糖核酸酶处理后,用YOYO-1或PicoGreen测试的不同菌株的DNA分布G1峰的变异系数总体上表明比Hoechst 33342染色有所改善。这些新型染料可用于通过流式细胞术对原核细胞进行计数,如大肠杆菌所示。然而,它们对离子强度的敏感性使其不适用于天然样品中的细胞周期分析。