IN-SITU P-31 NUCLEAR-MAGNETIC-RESONANCE FOR OBSERVATION OF POLYPHOSPHATE AND CATABOLITE RESPONSES OF CHEMOSTAT-CULTIVATED SACCHAROMYCES-CEREVISIAE AFTER ALKALINIZATION

Citation
Cd. Castro et al., IN-SITU P-31 NUCLEAR-MAGNETIC-RESONANCE FOR OBSERVATION OF POLYPHOSPHATE AND CATABOLITE RESPONSES OF CHEMOSTAT-CULTIVATED SACCHAROMYCES-CEREVISIAE AFTER ALKALINIZATION, Applied and environmental microbiology, 61(12), 1995, pp. 4448-4453
Citations number
21
Categorie Soggetti
Microbiology,"Biothechnology & Applied Migrobiology
ISSN journal
00992240
Volume
61
Issue
12
Year of publication
1995
Pages
4448 - 4453
Database
ISI
SICI code
0099-2240(1995)61:12<4448:IPNFOO>2.0.ZU;2-6
Abstract
The proposed pH buffering and phosphagenic functions of polyphosphate were investigated by subjecting chemostat-cultivated Saccharomyces cer evisiae to alkalinization (NaOH addition) and anaerobiosis, The subseq uent changes in intracellular phosphate-containing species were observ ed in situ by nuclear magnetic resonance (NMR) spectroscopy by using t he NMR cultivator we developed. For the alkalinization experiments, ch anges in catabolite secretion were also measured in parallel experimen ts, Additionally, a range of potential neutralization capacity was inv estigated: a dilute culture and concentrated cultures with low or high polyphosphate content. The concentrated cultures displayed increased cytosolic pH and rapid polyphosphate degradation to small chains. The pH changes and extent of polyphosphate degradation depended inversely on initial poly phosphate content. The dilute culture restored extrace llular pH rapidly and secreted acetate, The concentrated culture with low polyphosphate reserves also secreted acetate, In contrast to the a lkalinization-induced polyphosphate dynamics, anaerobiosis resulted in the complete hydrolysis of polyphosphate to P-i, as opposed to small chains, and reduced cytosolic pH. The results and calculations suggest that the bulk of NMR-observable polyphosphate (vacuolar) degradation to short polymers conceivably contributes to neutralizing added alkali nity, In other circumstances, such as anaerobiosis, degradation serves other functions, such as phosphorylation potential regulation.