scholarly journals CHROMATOGRAPHIC SEPARATION OF PEPTIDES-PROTEINS FROM Microcystis aeruginosa

Author(s):  
Seda Kusoglu
2020 ◽  
Vol 85 ◽  
pp. 47-58
Author(s):  
Y Jiang ◽  
Y Liu

Various studies have observed that increased nutrient supply promotes the growth of bloom-forming cyanobacteria, but only a limited number of studies have investigated the influence of increased nutrient supply on bloom-forming cyanobacteria at the proteomic level. We investigated the cellular and proteomic responses of Microcystis aeruginosa to elevated nitrogen and phosphorus supply. Increased supply of both nutrients significantly promoted the growth of M. aeruginosa and the synthesis of chlorophyll a, protein, and microcystins. The release of microcystins and the synthesis of polysaccharides negatively correlated with the growth of M. aeruginosa under high nutrient levels. Overexpressed proteins related to photosynthesis, and amino acid synthesis, were responsible for the stimulatory effects of increased nutrient supply in M. aeruginosa. Increased nitrogen supply directly promoted cyanobacterial growth by inducing the overexpression of the cell division regulatory protein FtsZ. NtcA, that regulates gene transcription related to both nitrogen assimilation and microcystin synthesis, was overexpressed under the high nitrogen condition, which consequently induced overexpression of 2 microcystin synthetases (McyC and McyF) and promoted microcystin synthesis. Elevated nitrogen supply induced the overexpression of proteins involved in gas vesicle organization (GvpC and GvpW), which may increase the buoyancy of M. aeruginosa. Increased phosphorus level indirectly affected growth and the synthesis of cellular substances in M. aeruginosa through the mediation of differentially expressed proteins related to carbon and phosphorus metabolism. This study provides a comprehensive description of changes in the proteome of M. aeruginosa in response to an increased supply of 2 key nutrients.


1962 ◽  
Vol 41 (2) ◽  
pp. 234-246 ◽  
Author(s):  
H. J. van der Molen

ABSTRACT A procedure for the quantitative determination of 5β-pregnan-3α-ol-20-one in urine is described. After acid hydrolysis of the pregnanolone-conjugates in urine, the free steroids are extracted with toluene. Pregnanolone is isolated in a pure form as its acetate; after chromatographic separation of the free steroids on alumina, the fraction containing pregnanolone is acetylated and rechromatographed on alumina. Quantitative determination of the isolated pregnanolone-acetate is carried out with the aid of the infrared spectrum recorded by a micro KBr-wafermethod. The reliability of the method under various conditions is discussed under the headings, specificity, accuracy, precision and sensitivity. It is possible to determine 30–40 μg pregnanolone in a 24-hours urine portion with a precision of 25%.


2003 ◽  
Vol 16 (4) ◽  
pp. 286-288 ◽  
Author(s):  
Andrej Oriňák ◽  
Monika Ádámová ◽  
Ladislav Halás ◽  
Peter Tomčík ◽  
Martina Justinová

2002 ◽  
Vol 15 (5) ◽  
pp. 341-344 ◽  
Author(s):  
Helena Majstorović ◽  
Živoslav Tešić ◽  
Dušanka Milojković-Opsenica

2004 ◽  
Vol 17 (1) ◽  
pp. 9-13 ◽  
Author(s):  
Helena Majstorović ◽  
Danijela Ratkov-Žebeljan ◽  
Živoslav Tešić ◽  
Dušanka Milojković-Opsenica

2019 ◽  
Vol 46 (1) ◽  
pp. 73-84
Author(s):  
L. Zhou ◽  
S. Nakai ◽  
G. F. Chen ◽  
Q. Pan ◽  
N. X. Cui ◽  
...  

2018 ◽  
Vol 43 (2) ◽  
pp. 265-274 ◽  
Author(s):  
W.X. Hong ◽  
S.P. Zuo ◽  
L.T. Ye ◽  
B.Q. Qin

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