The herbicide-resistant D1 mutant L275F of Chlamydomonas reinhardtii fails to show the bicarbonate-reversible formate effect on chlorophyll a fluorescence transients View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

1991-03

AUTHORS

Govindjee, Beatrix Schwarz, Jean David Rochaix, Reto J. Strasser

ABSTRACT

Herbicide-resistant mutants of the eukaryotic green alga Chlamydomonas reinhardtii, that are altered in specific amino acids in their D-1 protein, show differential bicarbonate-reversible formate effects. These results suggest the involvement of D1 protein in the ‘bicarbonate effect’. A 25 mM formate treatment of mixotrophically or photoautotrophically grown wild type cells results in a slower rise of chlorophyll a fluorescence transient followed by a dramatically slowed decline during measurements in continuous light. These effects are fully reversed upon addition of 10 mM bicarbonate. The mutant BR-202 [L275F] is, however, highly insensitive to 25 mM formate suggesting that a significant change in formate (bicarbonate) binding has occurred in helix V of the D1 protein near histidine involved in Fe binding. With the exception of DCMU-4 [S264A], which is considerably more sensitive to formate than the wild type, five other different [V219I, A25IV, F255Y, G256D and cell-wall deficient CW-15] mutants display a relatively similar response to formate as wild type. Absence of formate effect on a PS II-lacking [FuD-7] mutant confirms the sole involvement of PS II in the ‘bicarbonate effect’. More... »

PAGES

199-208

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00035841

DOI

http://dx.doi.org/10.1007/bf00035841

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1078840001

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/24414692


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