Variations of the Surface Sculpture and Cell Wall Ultrastructure of the Zygospores in Chlamydomonas geitleri (Chlorophyta)

The superficial cell wall ornamentation in the zygospores of the alga Chlamydomonas geitleri Ettl (Chlorophyta) is formed by thickenings of the cell wall which are shaped into a network of anastomosing ribs, sometimes with local wart-like protuberances. Clearly different sculpture patterns (given by presence, arrangement and/or morphological modification of sculpture elements) were accompanied by many transient forms. Sculpture variations occurred even in clonal cultures. In the zygospore cell wall of C. geitleri, the inner, outer and middle layer can be distinguished from the morphological point of view. The relatively thin outer (sporopollenin) layer covers the whole surface of the zygospore wall. The thicker inner layer adhering to the zygospore protoplast forms, either solely or together with the middle layer (possessing a fine meshwork substructure), variously shaped thickening of the zygospore cell wall. Discussed are the ultrastructural morphology of the cell wall in Chlamydomonas zygospores, the striking similarity of the cell wall ultrastructure of zygospores in C. geitleri to the ultrastructure of the cell wall of vegetative cells in some green algae (subfamily Scotiellocystoideae), as well as the extensive morphological variability of the zygospore wall sculpture in C geitleri and its species specificity.     

Comparative electrophoretic study on ribosomal proteins from algae

The proteins from cytoplasmic ribosomal subunits of eight species of algae were analyzed by two-dimensional gel electrophoresis. The molecular weights of the proteins were in the range of 10,000 to 55,000. We have compared the protein patterns from the ribosomal subunits of the different species to those of Chlamydomonas reinhardii. It was quite clear that there are many similarities in the protein patterns of all the investigated species. We found for Chlamydomonas eugametos 48, Chlamydomonas noctigama 42, Chlorogonium elongatum 47, Scenedesmus obliquus 40, Chlorella fusca 35, and Euglena gracilis 35 proteins which were homologous to those of Chlamydomonas reinhardii. For the colorless flagellate Polytoma papillatum, we detected 45 proteins homologous to Chlamydomonas reinhardii, so that the generally assumed close relationship between Chlamydomonas and Polytoma is confirmed.     

Do volvocal algae form their cultures as autonomous systems?

A low reproducibility of some characteristics in the life cycle of the volvocal algaChlamydomonas geitleri was observed in repeated experiments. The sets of the cultures were very similar in the number of the studied characteristics, but some of them differed significantly in one or several characteristics whereas the others agreed in a whole set. This is documented by the growth in a nitrogenless medium, the formation of zygotes, and their maturation and germination. The results of a small representative set of experiments were treated by an analysis of variance. Some possible explanations are discussed.     

Immunological studies of ferredoxin-nitrite reductases and ferredoxin-glutamate synthases from photosynthetic organisms

Polyclonal antiserum specific for ferredoxin-nitrite reductase (EC 1.7.7.1) from the green alga Chlamydomonas reinhardii recognized the nitrite reductase from other green algae, but did not cross-react with the corresponding enzyme from different cyanobacteria or higher plant leaves. An analogous situation was also found for ferredoxin-glutamate synthase (EC 1.4.7.1), using its specific antiserum. Besides, the antibodies raised against C. reinhardii ferredoxin-glutamate synthase were able to inactivate the ferredoxin-dependent activity of nitrite reductase from green algae.These results suggest that there exist similar domains in ferredoxin-nitrite reductases and ferredoxin-glutamate synthases from green algae. In addition, both types of enzymes share common antigenic determinants, probably located at the ferredoxin-binding domain. In spite of their physicochemical resemblances, no apparent antigenic correlation exists between the corresponding enzymes from green algae and those from higher plant leaves or cyanobacteria.Abbreviations Fd ferredoxin - GOGAT glutamate synthase - MV⁺ reduced methyl viologen (radical cation) - NiR nitrite reductase - PMSF phenylmethylsulphonyl fluoride - SDS sodium dodecyl sulfate     

Resolving the phylogenetic relationship between Chlamydomonas sp. UWO 241 and Chlamydomonas raudensis sag 49.72 (Chlorophyceae) with nuclear and plastid DNA sequences

The Antarctic psychrophilic green alga Chlamy‐domonas sp. UWO 241 is an emerging model for studying microbial adaptation to polar environments. However, little is known about its evolutionary history and its phylogenetic relationship with other chlamydomonadalean algae is equivocal. Here, we attempt to clarify the phylogenetic position of UWO 241, specifically with respect to Chlamydomonas rau‐densis SAG 49.72. Contrary to a previous report, we show that UWO 241 is a distinct species from SAG 49.72. Our phylogenetic analyses of nuclear and plastid DNA sequences reveal that UWO 241 represents a unique lineage within the Moewusinia clade (sensu Nakada) of the Chlamydomonadales (Chlorophyceae, Chlorophyta), closely affiliated to the marine species Chlamydomonas parkeae SAG 24.89.     

Bacteria and phosphorus regeneration in lakes. An experimental study

The aerobic decomposition of the green alga Chlamydomonas reinhardii by a mixed population of lake bacteria was studied in batch and chemostat cultures. Bacterial chemostats were supplied with continuously heatkilled algae. The dead algae rapidly released most of their phosphorus as SRP. In the batch experiments bacteria acted as consumers of the released algal phosphorus. This phosphorus uptake was dependent on the C:P ratio of the algae. During the death phase of the bacteria most of the bacterial phosphorus itself was released. The continuous supply of energy in form of dead algae in the chemostat experiments prevented the death phase of the bacteria and thus any net regeneration of phosphorus. The influence of the C:P stoichiometry of algae and bacteria on the regeneration of algal phosphorus is discussed.     

DNA-Binding Proteins and Structural Characteristics of Chloroplast Nucleoids

A comparative analysis of proteins from chloroplast nucleoids was performed in two higher-plant species (Pisum sativumL. andArabidopsis thalianaL.) and a green alga Chlamydomonas reinhardtiiDang. In the nucleoids of the higher plants and the alga, 26–27 proteins were detected with their mol wts ranging from 10 to more than 94 kD. In all the species tested, the distribution of nucleoid proteins by their mol wts was similar, especially between the predominant proteins with mol wts of 10 to 40 kD. Six DNA-binding proteins (12–18 kD) were detected in nucleoids fromCh. reinhardtiichloroplasts after in vivocovalent cross-linking between chloroplast DNA and proteins. Under an electron miscroscope, some regular structures resembling nucleosome-like particles of bacterial cells were revealed.     

Food selection by calanoid copepods in response to between-lake variation in food abundance

1. Food selection experiments were conducted by acclimating calanoid copepods (Eudiaptomus spp.) in suspensions of natural seston and then adding pairs of dual-labelled (¹⁴C/³²P) algae. Each feeding trial measured selectivity between a small, high-quality reference alga, Chlamydomonas reinhardii, and a test alga that differed in size and/or food quality. The influence of food concentration on food selection was tested by using seston from two lakes with contrasting food abundance and by including treatments with filtered lake water ('starved’) and seston diluted with filtered water or enriched with cultured algae. 2. Copepods that had been starved or acclimated to natural seston with low food abundance preferred the larger of two labelled algae, regardless of the nutritional quality of the algae. In agreement with the predictions of an optimal diet model, however, copepods that were acclimated to high food conditions discriminated against low-quality foods, including digestion-resistant algae and dead algae. 3. Selectivity coefficients showed excellent agreement with a previous study involving the same taxa of copepods and labelled algae but in which the copepods had been acclimated to pairs of cultured algae rather than natural seston. Thus, these comparisons emphasize the importance of food availability in modulating copepod selectivity for foods that differ in nutritional quality and suggest that such behaviour occurs in nature.     

Photooxidation of 3,3′-diaminobenzidine by blue-green algae and Chlamydomonas reinhardii

1.

1. The photooxidation of 3,3′-diaminobenzidine was investigated in whole cells of the wild-type and two mutant strains of Chlamydomonas reinhardii and in four species of blue-green algae.     

Untersuchungen an einer p-Aminobenzoesäure-Mangelmutante von Chlamydomonas reinhardii: Chloramphenicol als p-Aminobenzoesäure-Ersatz

Zusammenfassung Die p-Aminobenzoesäure-Mangelmutante pab 1 von Chlamydomonas reinhardii ist in der Lage, Chloramphenicol anstelle von p-Aminobenzoesäure als Supplementstoff zu verwenden. Es konnte jedoch gezeigt werden, daß die Algen selbst nicht imstande sind, Chloramphenicol zu p-Aminobenzoesäure abzubauen. Der Abbau erfolgt vielmehr spontan ohne Mitwirkung der Organismen, allerdings nur in belichteten Versuchsansätzen und nicht in Dunkelheit.Die Entstehung der p-Aminobenzoesäure geht über p-Nitrobenzaldehyd. Sie erfolgt rasch und reichlich, so daß für die Mutante ein Wachstum ermöglicht wird, das dem Wildtyp-Wachstum in Minimalmedium entspricht.

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Investigations on a p-Aminobenzoic auxotrophic mutant of Chlamydomonas reinhardii: Chloramphenicol as a substitute for p-aminobenzoic-acid

Summary The p-aminobenzoic-acid mutant pab 1 of Chlamydomonas reinhardii is able to use chloramphenicol as a supplement instead of p-aminobenzoic-acid. Nevertheless, it could be shown, that the algae are not in the position to reduce chloramphenicol to p-aminobenzoic-acid. On the contrary, the decomposition occurs spontaneously without the participation of the organisms, but only in experimental arrangements, exposed to light.The formation of the p-aminobenzoic-acid works rapidly and a high yield via p-nitrobenzaldehyde. Therefore the growth of the mutant is possible, corresponding to the growth of the wildtype cells in minimal-medium.

     

A linear DNA molecule of 5.9 kilobase-pairs is highly homologous to the chloroplast DNA in the green alga Chlamydomonas moewusii

Summary The unicellular green alga Chlamydomonas moewusii contains small DNA species of unknown cellular location. We report that the most abundant of these DNAs, here designated low-molecular-weight DNA (LMW DNA), is a linear molecule of 5.9 kilobase pairs (kbp). Southern blot hybridization and restriction enzyme analysis revealed that the LMW DNA sequence also exists as an integrated sequence in a discrete region of the chloroplast genome. We have confirmed earlier reports that small DNA species related to the LMW DNA are absent from Chlamydomonas eugametos, an alga which is interfertile with C. moewusii. In the C. eugametos chloroplast genome we found only remnants of the LMW DNA sequence.     

First DNA sequence of a chloroplast mutation: A missense alteration in the ribulosebisphosphate car☐ylase large subunit gene

Sequence comparison of the chloroplast genes of the large subunit of ribulosebisphosphate car☐ylase from wild-type and from a uniparental mutant of the green unicellular algaChlamydomonas reinhardii has revealed a single nucleotide change. The corresponding Gly to Asp amino acid substitution would introduce a negative charge into the presumptive substrate binding region of the enzyme and would explain the inactivity of the mutant protein. This is the first chloroplast mutation whose DNA sequence is known. Our results establish the first exact point of correlation between the physical map of the chloroplast genome ofC. reinhardii and a specific genetic locus.     

Potential importance of algae in the diet of adult Cyclops vicinus

• 1 The potential importance of phytoplankton to the nutrition of adult Cyclops vicinus was studied.
• 2 The flagellate Chlamydomonas reinhardii was ingested and digested at a higher rate than the coccale green alga Monoraphidium minutum.
• 3 The predation rate on the rotifer Brachionus rubens decreased if C. reinhardii was also available as food. No significant reduction of predation was found when M. minutum was offered together with B. rubens.
• 4 The species of available phytoplankton influenced egg production. Females which were allowed to feed on B. rubens and C. reinhardii produced more eggs than females which fed on rotifers only or a diet containing rotifers and M. minutum. Egg production was also possible when rotifers were absent from the diet.
• 5 Production efficiency was higher when C. reinhardii was the only food resource than on a diet containing rotifers only.

     

The mechanism of hydrogen photoproduction by several algae

Summary The contribution of PS II to H₂ photoproduction by several unicellular green algae was measured both when O₂ evolution and photophosphorylation were unimpaired and also when these processes had been eliminated by Cl-CCP. As judged by the effects of DCMU, a PS II contribution was found under both sets of experimental conditions for several strains of Chlorella, Ankistrodesmus and Scenedesmus. However, H₂ photoproduction by Chlamydomonas moewusii was insensitive to DCMU and thus was entirely due to PS I. With cells treated with Cl-CCP, the relative amount of PS II contribution varied from zero in autotrophically grown Chlamydomonas reinhardii, to 20% in photoheterotrophically grown and 50% in autotrophically grown cells of Ankistrodesmus braunii, Chlorella fusca, Chlorella vulgaris and Scenedesmus obliquus. The dehydrogenation of reduced H-donors by PS II of Scenedesmus treated with Cl-CCP showed the same biphasic kinetics previously described for H₂ photoproduction by PS I of this alga.Abbreviations Cl-CCP carbonyl cyanide m-chlorophenylhydrazone - DCMU 3-(3,4-dichlorophenyl)-1,1-dimethylurea - ICC Indiana Culture Collection - PS photosystem - SAL salicylaldoxime - SIO Marine Botany Culture Collection, Scripps Institution of Oceanography These studies were supported by contract No. AT-(40-1)-2687 from the U.S. Atomic Energy Commission.     

Mechanisms of response to salinity in halotolerant microalgae

Summary A limited number of organic solutes are used by microalgae to adjust their internal osmotic pressure in response to changing external salinities. Glycerol and proline are used by the most extremely halotolerant algae. Only glycerol allows growth at salinities approaching saturation. In addition to organic osmoregulatory solutes, inorganic ions also play an important role in osmoregulation. The ability of microalgae to maintain intracellular ions at levels compatible with metabolic functions may set upper limits for their salt tolerance. Requirements for NaCl in the external medium for nutrient transport may define the lower salinity limits for growth observed for some euryhaline algae.Osmotic upshocks generally cause severe temporary inhibition of photosynthesis in euryhaline microalgae. Extensive osmotic downshocks have little effect on photosynthesis in microalgae with strong cell walls, while wall-less species appear to be more sensitive. Rapid glycerol synthesis takes place in response to increased external salinity inChlamydomonas pulsatilla both in light and dark. Starch supplies carbon for glycerol synthesis in the dark and also during the initial periods of inhibition of photosynthesis in the light. Turnover of osmoregulatory solutes such as glycerol and isofloridoside may be an important aspect of the osmoregulatory mechanism.At salinities beyond the growth limit for the green flagellateChlamydomonas pulsatilla, resting spores are formed that enable this alga to survive extreme salinities.     

Stable nuclear transformation of Gonium pectorale

Background  

Green algae of the family Volvocaceae are a model lineage for studying the molecular evolution of multicellularity and cellular differentiation. The volvocine alga Gonium is intermediate in organizational complexity between its unicellular relative, Chlamydomonas, and its multicellular relatives with differentiated cell types, such as Volvox. Gonium pectorale consists of ~16 biflagellate cells arranged in a flat plate. The detailed molecular analysis of any species necessitates its accessibility to genetic manipulation, but, in volvocine algae, transformation procedures have so far only been established for Chlamydomonas reinhardtii and Volvox carteri.     

Ammonium (methylammonium) is the co-repressor of nitrate reductase in Chlamydomonas reinhardii

Methylammonium cannot be used as a nitrogen source by the green alga Chlamydomonas reinhardii and, like ammonia, caused the repression of nitrate reductase without affecting the photosynthetic activity. Glutamine synthetase catalyzed the conversion ofmethylammonium to a single product, identified as γ-N-methylglutamine, which accumulated in the cells. Derepression of nitrate reductase was accompanied by a decrease in the intracellular concentration of methylammonium and a concomitant accumulation of γ-N-methylglutamine inside the cells. These facts strongly suggest that ammonium (methylammonium) per se, and not a product of its metabolism, is the co-repressor of nitrate reductase in C. reinhardii     

Protein adaptation to low temperatures: a comparative study of α-tubulin sequences in mesophilic and psychrophilic algae

The α-tubulin genes from two psychrophilic algae belonging to the genus Chloromonas (here named ANT1 and ANT3) have been isolated and sequenced. The genes ant1 and ant3 contain 4 and 2 introns, respectively. The coding DNA sequences are 90% identical but the degree of isology is very high at the polypeptide level (more than 97% strict identities). The ANT1 and ANT3 α-tubulin amino acid sequences were compared to the corresponding sequence of the mesophilic alga Chlamydomonas reinhardtii. Of the 15 substitutions detected in ANT1 and/or ANT3, 5 are common to both psychrophilic algae. The recorded substitutions have been analyzed in terms of cold adaptation on the basis of the available three-dimensional structure of the α,β-tubulin heterodimer from pig brain. Most of these are subtle changes, but two substitutions, M268V and A295V occurring in the region of interdimer contacts, could be of great significance for the cold stability of Antarctic algae microtubules due to the fact that the entropic control of microtubule assembly is particularly high in cold adaptes species. Received: December 24, 1998 / Accepted: April 2, 1999     

Taxonomic study of a new green alga,Annulotesta cochlephila gen. et sp. nov. (Kornmanniaceae,Ulvales, Ulvophyceae), growing on the shells of door snails

Some algae are known to grow on shellfish shells. Most of these have been reported in aquatic environments. The species specificity for substrate shells varies, and some algae grow only on the shells of a certain species of shellfish, such as Pseudocladophora conchopheria (Cladophorales, Ulvophyceae) on Lunella coreensis (Trochida, Gastropoda). There are very few reports of algae that grow on land snails. In this study, we discovered green algae growing on the shells of six species of door snails (Clausiliidae) from nine localities in Japan. These green algae formed a green mat composed of thalli embedded in the extracellular matrix. The thallus was composed of aggregated oval cells and peripheral branched filaments. The cells possessed a single parietal chloroplast with a pyrenoid surrounded by two starch sheaths and transversed by a thylakoid. Oil droplets in the cell and ring-like structures on the cell wall surface were frequently observed. The 18S rDNA sequences of all shell-attached algae on different clausiliid species from different localities were almost identical and formed a new clade in the family Kornmanniaceae (Ulvales, Ulvophyceae). No other algae forming visible colonies on the clausiliid shell were found. These findings indicate the presence of specificity between the alga and clausiliid shells. Based on the results of morphological observation and molecular phylogenetic analysis, we propose a new genus and new species of shell-attached green alga, Annulotesta cochlephila.

     

Universal genetic code evidenced in mitochondria ofChlamydomonas reinhardii

Summary With the ultimate intent to establish a transformation system for eukaryotic organelles, the structure and organization of mitochondrial genes from the unicellular algaChlamydomonas reinhardii has been investigated. Using DNA hybridisation and DNA sequencing techniques, 3.9 kb of DNA, comprising about 25% of the mitochondrial genome, have been analysed in detail. By comparing the primary structure of homologous genes from other eukaryotic systems, we were able to identify the continuous genes coding for cytochrome oxidase subunit I (COI) and a NADH dehydrogenase subunit (ND5). The two genes are coded by opposite DNA strands and are not overlapping. The COI and the ND5 genes code for 505 and 567 amino acids, respectively. Interestingly, the comparative analysis with homologous genes from other eukaryotes shows that the universal genetic code is used in mitochondria ofC. reinhardii. This situation is different from all other mitochondrial systems studied so far. The results provide evidence thatC. reinhardii would be the appropriate organism for development of a transformation and expression system, where foreign genes, translated via the universal genetic code, are introduced into mitochondria.