Salzman G C, Griffith J K, Gregg C T
Appl Environ Microbiol. 1982 Nov;44(5):1081-5. doi: 10.1128/aem.44.5.1081-1085.1982.
There is a pressing need in clinical medicine for rapid identification of microorganisms. We describe a method that has the potential for such rapid identification: circular-intensity differential scattering, which is based on the differential scattering of left and right circularly polarized light. The scanning time required to obtain the spectral signature of an organism is about 4 min. Using a commercial circular dichrograph modified to measure circular intensity differential scattering at 90 degrees, we obtained significantly different spectra for five different crude influenza viruses. Salmonella typhimurium TA98 and TA100, and Escherichia coli HB101, HB101(pBR322), and HB101(pMB9). Purified supercoiled plasmid pBR322 DNA was readily distinguishable from linear pBR322 DNA; such differences in nucleic acid packaging may be significant factors in the discriminatory power of this technique.
临床医学迫切需要快速鉴定微生物。我们描述了一种有潜力实现这种快速鉴定的方法:圆强度差散射,它基于左旋和右旋圆偏振光的差散射。获得生物体光谱特征所需的扫描时间约为4分钟。使用一台经过改装以测量90度圆强度差散射的商用圆二色仪,我们获得了五种不同的粗流感病毒、鼠伤寒沙门氏菌TA98和TA100,以及大肠杆菌HB101、HB101(pBR322)和HB101(pMB9)的显著不同的光谱。纯化的超螺旋质粒pBR322 DNA很容易与线性pBR322 DNA区分开来;核酸包装的这种差异可能是该技术鉴别能力的重要因素。