A basic, economical and reproducible change strategy was created for Gram-positive microorganisms. It depended on fomentation of bacterial protoplasts with glass dots within the sight of DNA and polyethylene glycol. By utilizing this strategy, presentation of pGK12 into protoplasts of a few strains of Gram-positive microbes was achieved. The trouble in bringing DNA into cells of Gram-positive microorganisms is one of the main considerations that prevents hereditary investigations of Gram-positive microscopic organisms. The thick peptidoglycan layer in their cell dividers is viewed as a likely hindrance to DNA take-up. Change of these life forms can't happen normally however can be cultivated by specific change strategies, for example, protoplast change and electroporation. Protoplast change was produced for enzymatic expulsion of the cell divider to make protoplasts. Within the sight of polyethylene glycol, DNA take-up by protoplasts is encouraged. It was produced for some Gram-positive microbes Because of its low and profoundly factor proficiency and tedious convention, this strategy is once in a while utilized. Directly, electroporation is the most ordinarily utilized change technique for Gram-positive microscopic organisms. It includes the utilization of high voltage electric beat of brief span to prompt the arrangement of transient pores in cell dividers and films. Under suitable conditions, DNA present in general condition may enter through the pores. This technique was effectively used to bring DNA into a few strains of Gram-positive microscopic organisms. In spite of the fact that electroporation can be utilized to change the microscopic organisms with high effectiveness, it can't be performed by little and less-prepared research facilities as a result of the prerequisite of costly and specific gear. In this investigation, glass dot change was proposed as a basic, reasonable and reproducible change strategy for Gram-positive microscopic organisms.