Logarithmic Growth Phase (logarithmic + growth_phase)

Distribution by Scientific Domains


Selected Abstracts


Transport of phosphatidylinositol 3-phosphate into the vacuole via autophagic membranes in Saccharomyces cerevisiae

GENES TO CELLS, Issue 6 2008
Keisuke Obara
Vps34, the sole PtdIns 3-kinase in yeast, is essential for autophagy. Here, we show that the lipid-kinase activity of Vps34 is required for autophagy, implying an essential role of its product PtdIns(3)P. The protein-kinase activity of Vps15, a regulatory subunit of the PtdIns 3-kinase complex, is also required for efficient autophagy. We monitored the distribution of PtdIns(3)P in living cells using a specific indicator, the 2xFYVE domain derived from mammalian Hrs. PtdIns(3)P was abundant at endosomes and on the vacuolar membrane during logarithmic growth phase. Under starvation conditions, we observed massive transport of PtdIns(3)P into the vacuole. This accumulation was dependent on the membrane dynamics of autophagy. Notably, PtdIns(3)P was highly enriched and delivered into the vacuole as a component of autophagosome membranes but not as a cargo enclosed within them, implying direct involvement of this phosphoinositide in autophagosome formation. We also found a possible enrichment of PtdIns(3)P on the inner autophagosomal membrane compared to the outer membrane. Based on these results we discuss the function of PtdIns(3)P in autophagy. [source]


The copper-resistant bacterium ACU isolated from the rhizosphere of Eichhornia crassipes (Mart.) increased the endurance of Potamogeton crispus L. to copper toxicity

JOURNAL OF APPLIED MICROBIOLOGY, Issue 4 2008
L. Zhang
Abstract Aims:, This study aimed to develop endurance to copper stress in Potamogeton crispus L. by inoculation with the anti-copper strain ACU , a novel Enterobacteriaceae bacterium isolated from the rhizosphere of Eichhornia crassipes with high copper-removal ability. Methods and Results:, A spherical copper-resistant bacterium, namely ACU, was isolated from the rhizosphere of E. crassipes. It was demonstrated to have substantial copper-removing capability, even at copper concentrations as high as 69 mg l,1. The 16S rRNA gene sequence of ACU suggested it to be a novel Enterobacteriaceae bacterium most closely related to Providencia sp. With increasing copper concentrations, the growth rate of ACU gradually decreased with a delay in the logarithmic growth phase. ACU demonstrated high copper-removal ability at the lag phase when cultivated in media with high copper concentrations. A 48-kDa extracellular copper-binding protein was detected in ACU. When P. crispus was inoculated with ACU, the growth ability of P. crispus significantly improved at all the tested copper concentrations, and the lethal time for 10 mg l,1 was delayed. Further study revealed that while ACU cells were rarely detected in the culture solution, they were associated with the surface of P. crispus. These findings indicated that ACU grew by anchoring itself on the surface of P. crispus and could increase the ability of P. crispus to resist copper toxicity. Conclusion:, To the best of our knowledge, the Enterobacteriaceae bacterium ACU is a novel nonpathogenic bacterium with high copper-removing ability from water. Significance and Impact of the Study:, This study demonstrated that the Enterobacteriaceae bacterium ACU has potential applicability for use in copper removal and in the protection of aquatic plants in copper-polluted water. [source]


Salt- and glyphosate-induced increase in glyoxalase I activity in cell lines of groundnut (Arachis hypogaea)

PHYSIOLOGIA PLANTARUM, Issue 4 2002
Mukesh Jain
Glyoxalase I (EC 4.4.1.5) activity has long been associated with rapid cell proliferation, but experimental evidence is forthcoming, linking its role to stress tolerance as well. Proliferative callus cultures of groundnut (Arachis hypogaea L. cv. JL24) showed a 3.3-fold increase in glyoxalase I activity during the logarithmic growth phase, correlating well with the data on FW gain and mitotic index. Inhibition of cell division decreased glyoxalase I activity and vice versa, thus further corroborating its role as a cell division marker enzyme. Cell lines of A. hypogaea selected in the presence of high salt (NaCl) and herbicide (glyphosate) concentrations, yielded 4.2- to 4.5-fold and 3.9- to 4.6-fold elevated glyoxalase I activity, respectively, in a dose dependent manner reflective of the level of stress tolerance. The stress-induced increase in enzyme activity was also accompanied by an increase in the glutathione content. Exogenous supplementation of glutathione could partially alleviate the growth inhibition of callus cultures induced by methylglyoxal and d -isoascorbic acid, but failed to recover the loss in glyoxalase I activity due to d -isoascorbic acid. The adaptive significance of elevated glyoxalase I activity in maintaining glutathione homeostasis has been discussed in view of our understanding on the role of glutathione in the integration of cellular processes with plant growth and development under stress conditions. [source]


Adipose-derived stem cell: a better stem cell than BMSC

CELL BIOCHEMISTRY AND FUNCTION, Issue 6 2008
Yanxia Zhu
Abstract To further study the proliferation and multi-differentiation potentials of adipose-derived stem cells (ADSCs), the cells were isolated with improved methods and their growth curves were achieved with cck-8. Surface protein expression was analyzed by flow cytometry to characterize the cell phenotype. The multi-lineage potential of ADSCs was testified by differentiating cells with adipogenic, chondrogenic, osteogenic, and myogenic inducers. The results showed that about 5,×,105 stem cells could be obtained from 400 to 600,mg adipose tissue. The ADSCs can be continuously cultured in vitro for up to 1 month without passage and they have several logarithmic growth phases during the culture period. Also, the flow cytometry analysis showed that ADSCs expressed high levels of stem cell-related antigens (CD13, CD29, CD44, CD105, and CD166), while did not express hematopoiesis-related antigens CD34 and CD45, and human leukocyte antigen HLA-DR was also negative. Moreover, stem cell-related transcription factors, Nanog, Oct-4, Sox-2, and Rex-1 were positively expressed in ADSCs. The expression of alkaline phosphatase (ALP) was detected in the early osteogenic induction and the calcified nodules were observed by von Kossa staining. Intracellular lipid droplets could be observed by Oil Red staining. Differentiated cardiomyocytes were observed by connexin43 fluorescent staining. In order to obtain more stem cells, we can subculture ADSCs every 14 days instead of the normal 5 days. ADSCs still keep strong proliferation ability, maintain their phenotypes, and have stronger multi-differentiation potential after 25 passages. Copyright © 2008 John Wiley & Sons, Ltd. [source]