A variety of hyperthermophilic bacteria and archaea(1) have been isola
ted from high-temperature environments by plating and serial dilutions
(2). However, these techniques allow only the small percentage of orga
nisms able to form colonies, or those that are predominant within envi
ronmental samples, to be obtained in pure culture, Recently, in situ 1
6S ribosomal RNA analyses of samples from the Obsidian hot pool at Yel
lowstone National Park, Wyoming, revealed a variety of archaeal sequen
ces, which,were all different from those of previously isolated specie
s(3,4). This suggests substantial diversity of archaea with so far unk
nown morphological, physiological and biochemical features, which may
play an important part within high-temperature ecosystems, Here we des
cribe a procedure to obtain pure cultures of unknown organisms harbour
ing specific 16S rRNA sequences identified previously within the envir
onment, It combines visual recognition of single cells by phylogenetic
staining(5-9) and cloning by 'optical tweezers'(10,11). Our result va
lidates polymerase chain reaction data on the existence of large archa
eal communities.