Standard

A possible molecular mechanism of Chlamydomonas reinhardtii adaptation to different trophic conditions. / Пузанский, Роман Константинович; Романюк, Д.А.; Шаварда, Алексей Леонидович; Емельянов, Владислав Владимирович; Шишова, Мария Федоровна.

в: Protistology, Том 15, № 3, 01.01.2021, стр. 170-189.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

APA

Vancouver

Author

BibTeX

@article{9aad05995dfc48ad9f38ca228e89fa74,
title = "A possible molecular mechanism of Chlamydomonas reinhardtii adaptation to different trophic conditions",
abstract = "Microalgae are able to metabolize exogenous organic substrates. Differences in sets of available sources of energy and carbon cause various metabolic and physiological alterations. To characterize those in Chlamydomonas reinhardtii, we compared cells fed with acetate in batch cultures of CC-124 (wt-light) and CC-981 (mutant deficient in phosphoribulokinase, incapable to fix CO 2), growing under illumination (prk-light) or in the darkness (prk-dark). The growth intensity of the wt-light culture was higher only at the beginning of the culture cycle. Its final density only slightly exceeded such of prk-light ones. The growth rate and final density of the prk-dark culture were several times lower. The GC-MS analysis revealed clear metabolomic differences in cultures with different trophic status. Cells of prk-light were characterized by higher content of fatty acids, sterols, glycolate, malate, and putrescine. Cells of prk-dark accumulated, in particular, relatively higher levels of arginine, ornithine, AMP, some other nitrogen-containing compounds, glycerol, citrate, and sucrose. Higher levels of some amino acids and threonic acid were detected in wt-light cells. Simultaneously, we tested expression of genes encoding key enzymes of plant metabolism. The expression of RBCS1 (Rubisco small subunit), CIS1, 2 (citrate synthase), AAA1 (chloroplast ATP/ADP antiporter), APE2 (triose phosphate translocator), OMT1 (oxoglutarate/malate antiporter) was analyzed. The comparison revealed that RBCS1 was drastically upregulated in prk-light cultures. The expression level of AAA1 in prk-dark cells slightly exceeded such in wt-light algae, but was almost zero in prk-light cells. The level of CIS1, 2, APE2 and OMT1 was maximal in wt-light cells. ",
keywords = "Acetate, Batch culture, Chlamydomonas, Heterotrophic, Metabolomics, Mixotrophic, Prk1",
author = "Пузанский, {Роман Константинович} and Д.А. Романюк and Шаварда, {Алексей Леонидович} and Емельянов, {Владислав Владимирович} and Шишова, {Мария Федоровна}",
note = "Publisher Copyright: {\textcopyright} 2021 The Author(s)",
year = "2021",
month = jan,
day = "1",
doi = "10.21685/1680-0826-2021-15-3-7",
language = "English",
volume = "15",
pages = "170--189",
journal = "Protistology",
issn = "1680-0826",
publisher = "Protozoological Society Affiliated With The Russian Academy Of Sciences",
number = "3",

}

RIS

TY - JOUR

T1 - A possible molecular mechanism of Chlamydomonas reinhardtii adaptation to different trophic conditions

AU - Пузанский, Роман Константинович

AU - Романюк, Д.А.

AU - Шаварда, Алексей Леонидович

AU - Емельянов, Владислав Владимирович

AU - Шишова, Мария Федоровна

N1 - Publisher Copyright: © 2021 The Author(s)

PY - 2021/1/1

Y1 - 2021/1/1

N2 - Microalgae are able to metabolize exogenous organic substrates. Differences in sets of available sources of energy and carbon cause various metabolic and physiological alterations. To characterize those in Chlamydomonas reinhardtii, we compared cells fed with acetate in batch cultures of CC-124 (wt-light) and CC-981 (mutant deficient in phosphoribulokinase, incapable to fix CO 2), growing under illumination (prk-light) or in the darkness (prk-dark). The growth intensity of the wt-light culture was higher only at the beginning of the culture cycle. Its final density only slightly exceeded such of prk-light ones. The growth rate and final density of the prk-dark culture were several times lower. The GC-MS analysis revealed clear metabolomic differences in cultures with different trophic status. Cells of prk-light were characterized by higher content of fatty acids, sterols, glycolate, malate, and putrescine. Cells of prk-dark accumulated, in particular, relatively higher levels of arginine, ornithine, AMP, some other nitrogen-containing compounds, glycerol, citrate, and sucrose. Higher levels of some amino acids and threonic acid were detected in wt-light cells. Simultaneously, we tested expression of genes encoding key enzymes of plant metabolism. The expression of RBCS1 (Rubisco small subunit), CIS1, 2 (citrate synthase), AAA1 (chloroplast ATP/ADP antiporter), APE2 (triose phosphate translocator), OMT1 (oxoglutarate/malate antiporter) was analyzed. The comparison revealed that RBCS1 was drastically upregulated in prk-light cultures. The expression level of AAA1 in prk-dark cells slightly exceeded such in wt-light algae, but was almost zero in prk-light cells. The level of CIS1, 2, APE2 and OMT1 was maximal in wt-light cells.

AB - Microalgae are able to metabolize exogenous organic substrates. Differences in sets of available sources of energy and carbon cause various metabolic and physiological alterations. To characterize those in Chlamydomonas reinhardtii, we compared cells fed with acetate in batch cultures of CC-124 (wt-light) and CC-981 (mutant deficient in phosphoribulokinase, incapable to fix CO 2), growing under illumination (prk-light) or in the darkness (prk-dark). The growth intensity of the wt-light culture was higher only at the beginning of the culture cycle. Its final density only slightly exceeded such of prk-light ones. The growth rate and final density of the prk-dark culture were several times lower. The GC-MS analysis revealed clear metabolomic differences in cultures with different trophic status. Cells of prk-light were characterized by higher content of fatty acids, sterols, glycolate, malate, and putrescine. Cells of prk-dark accumulated, in particular, relatively higher levels of arginine, ornithine, AMP, some other nitrogen-containing compounds, glycerol, citrate, and sucrose. Higher levels of some amino acids and threonic acid were detected in wt-light cells. Simultaneously, we tested expression of genes encoding key enzymes of plant metabolism. The expression of RBCS1 (Rubisco small subunit), CIS1, 2 (citrate synthase), AAA1 (chloroplast ATP/ADP antiporter), APE2 (triose phosphate translocator), OMT1 (oxoglutarate/malate antiporter) was analyzed. The comparison revealed that RBCS1 was drastically upregulated in prk-light cultures. The expression level of AAA1 in prk-dark cells slightly exceeded such in wt-light algae, but was almost zero in prk-light cells. The level of CIS1, 2, APE2 and OMT1 was maximal in wt-light cells.

KW - Acetate

KW - Batch culture

KW - Chlamydomonas

KW - Heterotrophic

KW - Metabolomics

KW - Mixotrophic

KW - Prk1

UR - http://www.scopus.com/inward/record.url?scp=85118980326&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/8f92d16e-6274-323e-a80f-9a4beb49c50d/

U2 - 10.21685/1680-0826-2021-15-3-7

DO - 10.21685/1680-0826-2021-15-3-7

M3 - Article

VL - 15

SP - 170

EP - 189

JO - Protistology

JF - Protistology

SN - 1680-0826

IS - 3

ER -

ID: 86540810