According to metagenomics, DNA is extracted from a mixture of microbial community in soil, cloned into a vector and later on a metagenomic library is constructed. the ability of the community to produce a specific protein or antibiotic is also tested. However my doubt is that how the specific organism of interest can be isolated from the metagenome library which has hundreds of microbial community. there also exists a possibility that we may not know the primer sequence for a novel microorganism not yet studied which may be producing the specific antibiotic.Can somebody make this point clear to me