We examined the proportions of major Betaproteobacteria subgroups within bacterial communities in diverse nonaxenic, monospecific cultures of algae or cyanobacteria: four species of cryptophyta (genera Cryptomonas and Rhodomonas), four species of chlorophyta (genera Pediastrum, Staurastrum, and Chlamydomonas), and two species of cyanobacteria (genera Dolichospermum and Aphanizomenon). In the cryptophyta cultures, Betaproteobacteria represented 48 to 71% of total bacteria, the genus Limnohabitans represented 18 to 26%, and the Polynucleobacter B subcluster represented 5 to 16%. In the taxonomically diverse chlorophyta group, the genus Limnohabitans accounted for 7 to 45% of total bacteria. In contrast, cyanobacterial cultures contained significantly lower proportions of the Limnohabitans bacteria (1 to 3% of the total) than the cryptophyta and chlorophyta cultures. Notably, largely absent in all of the cultures was Polynucleobacter necessarius (Polynucleobacter C subcluster). Subsequently, we examined the growth of Limnohabitans strains in the presence of different algae or their extracellular products (EPP). Two strains, affiliated with Limnohabitans planktonicus and Limnohabitans parvus, were separately inoculated into axenic cultures of three algal species growing in an inorganic medium: Cryptomonas sp., Chlamydomonas noctigama, and Pediastrum boryanum. The Limnohabitans strains cocultured with these algae or inoculated into their EPP consistently showed (i) pronounced population growth compared to the control without the algae or EPP and (ii) stronger growth stimulation of L. planktonicus than of L. parvus. Overall, growth responses of the Limnohabitans strains cultured with algae were highly species specific, which suggests a pronounced niche separation between two closely related Limnohabitans species likely mediated by different abilities to utilize the substrates produced by different algal species.There is compelling evidence that phytoplankton community dynamics have a significant impact on the composition of bacterioplankton communities (for example, see references 6, 19, and 21). The apparent driving force of such alga-bacterium interactions is likely the nature and quantity of alga-derived substrates available in the form of extracellular phytoplankton products (EPP) or decaying algal biomass. Although it is usually not known which algal species are the major EPP producers in situ, tight species-specific alga-bacterium relationships have been suggested as characterizing bacterium-alga consortia (e.g., 6, 21, 33). Interactions of phytoplankton and bacteria range from symbiotic to parasitic relationships (3). It is not surprising, then, that specific bacterial assemblages associated with different algae can also stimulate or even inhibit algal growth, as documented for cultures of marine diatoms (6). The latter study also demonstrated that free-living and phytoplankton-associated (i.e., attached to algal surfaces) bacteria are significantly different from each other and are dominated by distinct phylog...