Baldwin K A, McKay L L
Department of Food Science and Nutrition, University of Minnesota, St. Paul 55108.
J Dairy Sci. 1987 Oct;70(10):2005-12. doi: 10.3168/jds.S0022-0302(87)80247-3.
Transduction for lactose-fermenting ability between the lactose-positive lysogen Streptococcus lactis LM0221 and plasmid-cured, prophage-cured, lactose-negative S. lactis LM2301 resulted in the appearance of lactose-positive transductants surrounded by a zone of clearing in the lactose-negative cell lawn. By using plaque assay procedures, the zones were shown to contain bacteriophage particles, and both spontaneous release and UV induction of prophage from these transductants were demonstrated. The DNA hybridization confirmed that LM2301 did not contain the prophage in its chromosome and that the zone-producing transductant KZ1 was relysogenized by the temperate bacteriophage. Further, a 4.35 Kb EcoRI digestion fragment appeared to contain the DNA sequences for integration into the chromosome and may provide a means for stabilizing cloned DNA by effecting chromosomal insertion in LM2301 derivatives. The selection of zone-producing lactose-positive transductants of LM2301 provided a means for detecting strains relysogenized by the temperate phage induced from LM0221.
在乳糖阳性溶原性乳酸乳球菌LM0221和质粒消除、原噬菌体消除、乳糖阴性的乳酸乳球菌LM2301之间进行乳糖发酵能力的转导,结果在乳糖阴性细胞菌苔中出现了被透明圈包围的乳糖阳性转导子。通过噬菌斑检测程序,表明这些透明圈含有噬菌体颗粒,并且证明了这些转导子中噬菌体的自发释放和紫外线诱导。DNA杂交证实LM2301的染色体中不含有原噬菌体,并且产生透明圈的转导子KZ1被温和噬菌体再次溶原化。此外,一个4.35 Kb的EcoRI消化片段似乎包含整合到染色体中的DNA序列,并且可能通过在LM2301衍生物中实现染色体插入来提供一种稳定克隆DNA的方法。选择LM2301产生透明圈的乳糖阳性转导子提供了一种检测被从LM0221诱导的温和噬菌体再次溶原化的菌株的方法。