02573nas a2200265   4500008004100000022001400041245010400055210006900159260001200228300001400240490000700254520177600261653002002037653002102057653001502078653001702093653002402110653001202134653002502146100001202171700002002183700001602203700002902219856005902248       2019                        eng d  a0948-305500aDrivers of protistan community autotrophy and heterotrophy in chemically stratified Antarctic lakes0 aDrivers of protistan community autotrophy and heterotrophy in ch  c01/2019  a225 - 2390 v823 a<p>Single-celled, eukaryotic microorganisms, known as protists, are responsible for 2 important, yet opposing, metabolic activities within aquatic food webs. They are major primary producers and highly active predators in marine and fresh water systems. While genomics has accelerated in recent years for this taxonomically diverse group, our understanding of the metabolic capabilities of most protists remains limited. It is also poorly understood how protist trophic mode is affected by biotic and abiotic factors, and therefore it is difficult to predict how events such as global climate change will affect the balance between autotrophic and heterotrophic activities in protist communities. To address open questions regarding how protist metabolic versatility is influenced by their environment, we characterized the potential for carbon fixation versus organic carbon degradation using enzymatic assays (RubisCO and β-D-glucosaminidase, respectively) within the water columns of ice-covered lakes in McMurdo Dry Valleys (MDV), Antarctica. Steep physical and chemical gradients in the water columns, microorganism domination and minimal allochthonous inputs makes the MDV lakes uniquely suited to investigate environment-microbe interactions. Spatial trends in RubisCO and β-D-glucosaminidase activities were lake-specific and vertically stratified within the water columns. Moreover, bottom-up drivers controlling the activity of C-fixation vs. organic C-degradation among the MDV protist communities were distinct between the upper photic vs. the deep, aphotic zones. We conclude that differential controls over major C-cycling enzymes have important implications on the influence of environmental change on the carbon and nutrient cycles in the MDV lakes.</p>10aAntarctic lakes10aAquatic protists10aAutotrophy10aHeterotrophy10aMcMurdo Dry Valleys10aRubisCO10aβ-D-glucosaminidase1 aLi, Wei1 aDolhi-Binder, J1 aCariani, ZE1 aMorgan-Kiss, Rachael, M.  uhttps://www.int-res.com/abstracts/ame/v82/n3/p225-239/03186nas a2200181   4500008004100000245010400041210006900145260003900214490001000253520255800263653002002821653001602841653002202857653001202879100002102891700002902912856006302941       2014                        eng d00aEnvironmental impacts on RubisCO from green algal laboratory isolates to Antarctic lake communities0 aEnvironmental impacts on RubisCO from green algal laboratory iso  aOxford, OHbMiami Universityc20140 vPh.D.3 a<p>Ribulose-1,5-bisphosphate carboxylase oxygenase (RubisCO) is found in a variety of autotrophic microorganisms ranging from green algae, cyanobacteria, and chemoautotrophic bacteria. As this enzyme has the potential to catalyze carboxylation (carbon fixation) or oxygenation (photorespiration) reactions, it is regulated in response to environmental variables at the levels of transcription, translation, and post-translation by the enzyme, RubisCO activase. A combination of laboratory experiments on green algal isolates and field experiments were utilized to gain insight on carbon fixation in permanently ice-covered Antarctic lakes. RubisCO was investigated as a potential target for cold adaptation of carbon fixation in the psychrophilic green alga, Chlamydomonas raudensis UWO241 (UWO241), isolated from Lake Bonney, Antarctica. RubisCO activity, stability, and whole cell carbon fixation were measured for the psychrophile and compared to a closely related mesophilic alga, C. raudensis SAG49.72 (SAG49.72). The effect of environmental factors including light and temperature on UWO241 and SAG49.72 RubisCO activation state, an indirect measurement of RubisCO activase activity, and abundance was investigated using a modified RubisCO carboxylase assay and immunoblotting, respectively. Lastly, maximum potential RubisCO carboxylase activity was determined using a modified activity assay in multiple ice covered Antarctic lakes including Lake Bonney. This data was complemented with lake depth profiles of enzyme abundance determined by quantitative real-time PCR and RubisCO-harboring organism diversity. While purified RubisCO of the psychrophilic green alga did not function optimally at low temperature, whole cell carbon fixation was greater under such conditions, suggesting that the overall process of carbon fixation is modified to function in UWO241. Increased RubisCO abundance at low temperature may contribute to this phenomenon. Low light levels may be important in regulation of RubisCO via RubisCO activase and should be further investigated. Based on community level RubsiCO activity and enzyme abundance, light and RubisCO harboring organisms including eukaryotic algae and cyanobacteria were positively correlated, but this was variable between lakes. Dark carbon fixation was potentially important in lakes west lobe Bonney and Fryxell and this community was negatively correlated with light. Results of targeted physiology and community level experiments led to development of a carbon fixation model for Lake Bonney.</p>10acarbon fixation10agreen algae10aice-covered lakes10aRubisCO1 aDolhi, Jenna, M.1 aMorgan-Kiss, Rachael, M.  uhttp://rave.ohiolink.edu/etdc/view?acc_num=miami1407056783