Panikov Nicolai S, Sizova Maria V
Department of Chemistry & Chemical Biology, Stevens Institute of Technology, NJ 07030, USA.
FEMS Microbiol Ecol. 2007 Feb;59(2):500-12. doi: 10.1111/j.1574-6941.2006.00210.x. Epub 2006 Oct 5.
We developed a procedure to culture microorganisms below freezing point on solid media (cellulose powder or plastic film) with ethanol as the sole carbon source without using artificial antifreezes. Enrichment from soil and permafrost obtained on such frozen solid media contained mainly fungi, and further purification resulted in isolation of basidiomycetous yeasts of the genera Mrakia and Leucosporidium as well as ascomycetous fungi of the genus Geomyces. Contrary to solid frozen media, the enrichment of liquid nutrient solutions at 0 degrees C or supercooled solutions stabilized by glycerol at -1 to -5 degrees C led to the isolation of bacteria representing the genera Polaromonas, Pseudomonas and Arthrobacter. The growth of fungi on ethanol-microcrystalline cellulose media at -8 degrees C was exponential with generation times of 4.6-34 days, while bacteria displayed a linear or progressively declining curvilinear dynamic. At -17 to -0 degrees C the growth of isolates and entire soil community on 14C-ethanol was continuous and characterized by yields of 0.27-0.52 g cell C (g of C-substrate)(-1), similar to growth above the freezing point. The 'state of maintenance,' implying measurable catabolic activity of non-growing cells, was not confirmed. Below -18 to -35 degrees C, the isolated organisms were able to grow only transiently for 3 weeks after cooling with measurable respiratory and biosynthetic (14CO2 uptake) activity. Then metabolic activity declined to zero, and microorganisms entered a state of reversible dormancy.
我们开发了一种程序,可在不使用人工防冻剂的情况下,以乙醇作为唯一碳源,在固体培养基(纤维素粉末或塑料薄膜)上于冰点以下培养微生物。从土壤和永久冻土中富集得到的此类冷冻固体培养基上主要含有真菌,进一步纯化后分离出了Mrakia属和Leucosporidium属的担子菌酵母以及Geomyces属的子囊菌。与固体冷冻培养基相反,在0℃的液体营养液或用甘油在-1至-5℃稳定的过冷溶液中富集,导致分离出了Polaromonas属、Pseudomonas属和Arthrobacter属的细菌。真菌在-8℃的乙醇-微晶纤维素培养基上的生长呈指数增长,代时为4.6-34天,而细菌则呈现线性或逐渐下降的曲线动态。在-17至-0℃时,分离菌株和整个土壤群落对14C-乙醇的生长持续进行,产量为0.27-0.52 g细胞碳/(g碳底物),与冰点以上的生长情况相似。未证实存在“维持状态”,即非生长细胞具有可测量的分解代谢活性。在-18至-35℃以下,分离出的生物体在冷却后仅能短暂生长3周,具有可测量的呼吸和生物合成(14CO2吸收)活性。然后代谢活性降至零,微生物进入可逆休眠状态。