Molnár J, Csiszár K, Nishioka I, Shoyama Y
Acta Microbiol Hung. 1986;33(3):221-31.
Some cannabispiro compounds and tetrahydrocannabidiolic acid were tested for antibacterial plasmid curing activity and inhibition of plasmid transfer. MIC values of the compound were above 1500 micrograms/ml. Cannabispirol and tetrahydrocannabidiolic acid eliminated the F'lac plasmid from Escherichia coli, but acetylcannabispirol, cannabispirone and cannabispirenone were ineffective as curing agents. Each compound, except acetyl-cannabispirol, selectively killed plasmid carrying bacteria. The compounds inhibited R144 plasmid transfer from E. coli into E. coli cells via inhibition of mating pair formation, zygotic killing and inhibition of transconjugal DNA synthesis in a lesser extent. All of the cannabispiro compounds and tetrahydrocannabidiolic acid inhibited the transformation with pBR322 plasmid DNA when the bacteria were pretreated with the compounds, via inhibition of the DNA penetration or decreasing the synthesis of plasmid DNA during bacterial growth. Although each of the compounds, except acetyl-cannabispirol, had a weak antibacterial effect which was more definite on plasmid carrying bacteria than plasmidless ones, and inhibited intercellular plasmid transfer and transforming activity of plasmid DNA, only two of them were able to cure F'lac plasmid showing that plasmid elimination is a complex process which strictly depends on the stereochemical configuration of curing agents.
对一些大麻螺环化合物和四氢大麻二酚酸进行了抗性质粒消除活性和质粒转移抑制作用的测试。该化合物的最低抑菌浓度(MIC)值高于1500微克/毫升。大麻螺酚和四氢大麻二酚酸可消除大肠杆菌中的F'lac质粒,但乙酰大麻螺酚、大麻螺酮和大麻螺烯酮作为消除剂无效。除乙酰大麻螺酚外,每种化合物都能选择性地杀死携带质粒的细菌。这些化合物通过抑制配对形成、合子杀伤以及在较小程度上抑制接合后DNA合成,抑制了R144质粒从大肠杆菌向大肠杆菌细胞的转移。当用这些化合物预处理细菌时,所有的大麻螺环化合物和四氢大麻二酚酸都通过抑制DNA渗透或减少细菌生长过程中质粒DNA的合成,抑制了pBR322质粒DNA的转化。尽管除乙酰大麻螺酚外的每种化合物都有微弱的抗菌作用,对携带质粒的细菌的作用比对无质粒细菌更明显,并且抑制细胞间质粒转移和质粒DNA的转化活性,但只有其中两种能够消除F'lac质粒,这表明质粒消除是一个复杂的过程,严格取决于消除剂的立体化学构型。