Entire Growth Cycle Research Articles

The Hidden Habit of the Entomopathogenic Fungus Beauveria bassiana: First Demonstration of Vertical Plant Transmission

Beauveria bassiana strain 04/01-Tip, obtained from a larva of the opium poppy stem gall wasp Iraella luteipes (Hymenoptera; Cynipidae), endophytically colonizes opium poppy (Papaver somniferum L.) plants and protects them against this pest. The goal of this study was to monitor the dynamics of endophytic colonization of opium poppy by B. bassiana after the fungus was applied to the seed and to ascertain whether the fungus is transmitted vertically via seeds. Using a species-specific nested PCR protocol and DNA extracted from surface-sterilised leaf pieces or seeds of B. bassiana-inoculated opium poppy plants, the fungus was detected within the plant beginning at the growth stage of rosette building and them throughout the entire plant growth cycle (about 120–140 days after sowing). The fungus was also detected in seeds from 50% of the capsules sampled. Seeds that showed positive amplification for B. bassiana were planted in sterile soil and the endophyte was again detected in more than 42% of the plants sampled during all plant growth stages. Beauveria bassiana was transmitted to seeds in 25% of the plants from the second generation that formed a mature capsule. These results demonstrate for the first time the vertical transmission of an entomopathogenic fungus from endophytically colonised maternal plants. This information is crucial to better understand the ecological role of entomopathogenic fungi as plant endophytes and may allow development of a sustainable and cost effective strategy for I. luteipes management in P. somniferum.

Ethylene Modulates the Developmental Plasticity and the Growth Balance Between Shoot and Root Systems in the In Vitro Grown Epiphytic Orchid Catasetum fimbriatum

The epiphytic habitat is potentially one of the most stressful environments for plants, making the effective developmental control in response to external cues critical for epiphyte survival. Because ethylene mediates several abiotic stresses in plants, here, we have examined the ethylene influence in both shoot and root systems of the epiphytic orchid Catasetum fimbriatum. Under controlled conditions, ethylene production was quantified during an entire growth cycle of C. fimbriatum development in vitro, while treatments modulating either ethylene concentration or perception were carried out over the early growth phase of these plants. After treatments, growth measurements and histological features were studied in both shoot and root tissues. Ethylene production showed a decreasing trend over the period of organ elongation; however, it increased considerably when leaves were shed, and a new axillary bud was initiating. The early exposure of young plants to higher concentrations of ethylene triggered morphogenic responses that included root hair formation instead of velamen, and a combination of inhibitory effects (decreases in both stem enlargement and cellular/organ elongation) and inductive effects (increases in leaf and root formation, bud initiation and cellular thickening) on plant growth, which favored biomass allocation to roots. Conversely, inhibition of ethylene perception over the plant growth phase generally resulted in the opposite morphogenic responses. Our data indicate that periodic variations in ethylene concentration and/or sensitivity seem to modulate several developmental features in shoot and root systems of C. fimbriatum which could have adaptive significance during the growing phase of this epiphytic orchid.

마이크로파 산란계를 이용한 밀 생육 추정

Microwave remote sensing can help monitor the land surface water cycle and crop growth. This type of remote sensing has great potential over conventional remote sensing using the visible and infrared regions due to its all-weather day-and-night imaging capabilities. In this paper, a ground-based multi-frequency (L-, C-, and X-band) polarimetric scatterometer system capable of making observations every 10 min was developed. This system was used to monitor the wheat over an entire growth cycle. The polarimetric scatterometer components were installed inside an air-conditioned shelter to maintain constant temperature and humidity during the data acquisition period. Backscattering coefficients for the crop growing season were compared with biophysical measurements. Backscattering coefficients for all frequencies and polarizations increased until dat of year 137 and then decreased along with fresh weight, dry weight, plant height, and vegetation water content (VWC). The range of backscatter for X-band was lower than for L- and C-band. We examined the relationship between the backscattering coefficients of each band (frequency/polarization) and the various wheat growth parameters. The correlation between the different vegetation parameters and backscatter decreased with increasing frequency. L-band HH-polarization (L-HH) is best suited for the monitoring of fresh weight (r=0.98), dry weight (r=0.96), VWC (r=0.98), and plant height (r=0.96). The correlation coefficients were highest for L-band observations and lowest for X-band. Also, HH-polarization had the highest correlations among the polarization channels (HH, VV and HV). Based on the correlation analysis between backscattering coefficients in each band and wheat growth parameters, we developed prediction equations using the L-HH based on the observed relationships between L-HH and fresh weight, dry weight, VWC and plant height. The results of these analyses will be useful in determining the optimum microwave frequency and polarizations necessary for estimating vegetation parameters in the wheat.

Tracking the Location and Dynamics of Chromosomal Loci in E. Coli

We have used widefield fluorescence microscopy to locate fluorescently labeled, specific DNA loci on the E. coli chromosome. Their cellular position, short and long-time motion were tracked with ∼30 nm accuracy. In addition to the conventional analysis of the location of the loci in the long axis of the cell, we have also analyzed their locations along the short axis. The origin of replication (oriC) has been postulated to be anchored to the cell membrane, which helps regulate the initiation of replication. In slow growth conditions the distributions of oriC and the other tested loci (including the rrn operon rrnD) in the short axis are peaked in the center. In moderate growth conditions they are peaked 200-300 nm away from the cell center. We examined the extent to which loci sample the entire nucleoid on a short timescale (1-3 s). Dynamics of each locus were studied for several hundred cells by tracking their position for several seconds. Similar to the other tested loci, in MBM oriC undergoes confined diffusion (D1 = 9.7 x 10−3 μm2s−1) in a ∼100 nm domain that itself diffuses further on a longer time scale (D2 = 7.8 x 10−4 μm2s−1). Foci were also tracked over the entire growth cycle. Periodic motion was observed in the short axis suggesting the DNA rotates as it segregates. The cytoskeletal protein MreB is known to rotate in the short axis and is dependent on cell wall assembly. When cells were treated with the MreB depolymerizing antibiotic A22 and cell wall growth inhibiting antibiotics, the oscillatory motion of the DNA loci was not disrupted. This suggests that loci oscillatory motion is not related to the observed rotation of MreB, but is driven by an as of yet undiscovered source.

RiceXPro Version 3.0: expanding the informatics resource for rice transcriptome

A wide range of resources on gene expression profiling enhance various strategies in plant molecular biology particularly in characterization of gene function. We have updated our gene expression profile database, RiceXPro (http://ricexpro.dna.affrc.go.jp/), to provide more comprehensive information on the transcriptome of rice encompassing the entire growth cycle and various experimental conditions. The gene expression profiles are currently grouped into three categories, namely, ‘field/development’ with 572 data corresponding to 12 data sets, ‘plant hormone’ with 143 data corresponding to 13 data sets and ‘cell- and tissue-type’ comprising of 38 microarray data. In addition to the interface for retrieving expression information of a gene/genes in each data set, we have incorporated an interface for a global approach in searching an overall view of the gene expression profiles from multiple data sets within each category. Furthermore, we have also added a BLAST search function that enables users to explore expression profile of a gene/genes with similarity to a query sequence. Therefore, the updated version of RiceXPro can be used more efficiently to survey the gene expression signature of rice in sufficient depth and may also provide clues on gene function of other cereal crops.

On the Retrieval of Soil Moisture in Wheat Fields From L-Band SAR Based on Water Cloud Modeling, the IEM, and Effective Roughness Parameters

The synthetic aperture radar (SAR)-based soil moisture retrieval of agricultural fields is often hampered by vegetation effects on the backscattered signal. The semiempirical water cloud model (WCM) allows for estimating the backscatter of a vegetated surface, accounting for both the contributions of the vegetation and the underlying soil. The latter is often described through the integral equation model (IEM). Unfortunately, the IEM requires an accurate parameterization of the surface roughness which is very difficult to achieve. Therefore, this letter extends the WCM with a bare soil contribution that is based on the IEM, which, however, relies on calibrated or effective roughness parameters. Furthermore, this letter compares a number of vegetation indicators for their use in the WCM. Based on a series of L-band SAR observations, it is shown that effective roughness parameters are a promising tool for soil moisture retrieval under a wheat canopy and that the use of a leaf area index may be recommended above other vegetation indicators, as it leads to the lowest root-mean-square errors of about 5.5 vol%. These results prove the operational potential of L-band SAR data for soil moisture inferred under a wheat canopy throughout the entire crop growth cycle.

L Band Brightness Temperature Observations over a Corn Canopy during the Entire Growth Cycle

During a field campaign covering the 2002 corn growing season, a dual polarized tower mounted L-band (1.4 GHz) radiometer (LRAD) provided brightness temperature (TB) measurements at preset intervals, incidence and azimuth angles. These radiometer measurements were supported by an extensive characterization of land surface variables including soil moisture, soil temperature, vegetation biomass, and surface roughness. In the period May 22 to August 30, ten days of radiometer and ground measurements are available for a corn canopy with a vegetation water content (W) range of 0.0 to 4.3 kg m−2. Using this data set, the effects of corn vegetation on surface emissions are investigated by means of a semi-empirical radiative transfer model. Additionally, the impact of roughness on the surface emission is quantified using TB measurements over bare soil conditions. Subsequently, the estimated roughness parameters, ground measurements and horizontally (H)-polarized TB are employed to invert the H-polarized transmissivity (γh) for the monitored corn growing season.

Evidence that sulfur metabolism plays a role in microcystin production by Microcystis aeruginosa

Microcystins (MCs) are highly toxic, non-ribosomal cyclic peptides produced by cyanobacteria. A wide range of environmental factors are known to affect MC production, yet the roles these factors play in MC metabolism are poorly understood. In this study a physiological role for sulfur in MC synthesis is proposed. Rates of amino acid and MC-LR production were determined from N-limited chemostat grown cells of the toxic cyanobacterium Microcystis aeruginosa MASH-01A19. Cluster analysis of these rates indicated a correlation between the rates of methionine and MC-LR production, suggesting that a competitive physiological requirement for this sulfur-containing metabolite may limit MC-LR production in this organism. In support of this hypothesis, sulfur limitation in batch cultures led to an approximate 1.5-fold decrease in the intracellular MC-LR quota ( Q MC) over the entire growth cycle, revealing a requirement for sulfur in MC production and suggesting that metabolic demand for methionine may limit MC synthesis.

Drought pretreatment increases the salinity resistance of tomato plants

AbstractAgricultural productivity is worldwide subjected to increasing salinity problems. Various strategies are applied to overcome the deleterious effects of salinity on plants. This study was conducted in order to determine whether drought pretreatment of seedlings or seed pretreatment with NaCl increases the long‐term salinity resistance of tomato (Solanum lycopersicum L.) and whether the adaptive response to salinity is accompanied by physiological changes throughout the plant‐growth cycle. When plants were pretreated at the five‐leaf growth stage, the plant dry weight was significantly higher in drought‐pretreated than in non‐pretreated plants after 50 d of salt treatment. The positive effect of drought pretreatment applied at the five‐leaf stage was maintained throughout the entire growth cycle, as fruit yield of drought‐pretreated plants was 40% higher than that of non‐pretreated plants at the end of the harvest period (150 d of 70 mM NaCl treatment). Moreover, the most productive plants maintained lower Na+ and Cl– accumulation in their leaves until the end of the growth cycle, which shows that adaptation is a long‐term response during which the plants adjust their physiology to the environmental conditions. Salt resistance was also improved through seed pretreatment with NaCl. In conclusion, drought pretreatment applied at the five‐leaf stage or seed pretreatment with NaCl provide an alternative way to enhance salt resistance in tomato, and the increase in yield is associated with physiological changes throughout the plant‐growth cycle.

Dynamics of Microbial Activity Related to N Cycling in Cd-Contaminated Soil During Growth of Soybean

The potential influences of cadmium (Cd) on the biochemical processes of the soil nitrogen (N) cycle, along with the dynamics of ammonification, nitrification, and denitrification processes in the rhizosphere and non-rhizosphere (bulk soil), respectively, were investigated in a Cd-stressed system during an entire soybean growing season. In terms of Cd pollution at the seedling stage, the ammonifying bacteria proved to be the most sensitive microorganisms, whereas the effects of Cd on denitrification were not obvious. Following the growth of soybeans, the influences of Cd on ammonification in the bulk soil were: toxic impacts at the seedling stage, stimulatory effects during the early flowering stage, and adaptation to the pollutant during the podding and ripening stages. Although nitrification and denitrification in the bulk soil decreased throughout the entire growth cycle, positive adaptation to Cd stress was observed during the ripening stage. Moreover, during the ripening stage, denitrification in the bulk soil under high Cd treatment (20 mg kg −1) was even higher than that in the control, indicating a probable change in the ecology of the denitrifying microbes in the Cd-stressed system. Changes in the activity of microbes in the rhizosphere following plant growth were similar to those in the non-rhizosphere in Cd treatments; however, the tendency of change in the rhizosphere seemed to be more moderate. This suggested that there was some mitigation of Cd stress in the rhizosphere.

Parameter stability of the functional-structural plant model GREENLAB as affected by variation within populations, among seasons and among growth stages.

It is increasingly accepted that crop models, if they are to simulate genotype-specific behaviour accurately, should simulate the morphogenetic process generating plant architecture. A functional-structural plant model, GREENLAB, was previously presented and validated for maize. The model is based on a recursive mathematical process, with parameters whose values cannot be measured directly and need to be optimized statistically. This study aims at evaluating the stability of GREENLAB parameters in response to three types of phenotype variability: (1) among individuals from a common population; (2) among populations subjected to different environments (seasons); and (3) among different development stages of the same plants. Five field experiments were conducted in the course of 4 years on irrigated fields near Beijing, China. Detailed observations were conducted throughout the seasons on the dimensions and fresh biomass of all above-ground plant organs for each metamer. Growth stage-specific target files were assembled from the data for GREENLAB parameter optimization. Optimization was conducted for specific developmental stages or the entire growth cycle, for individual plants (replicates), and for different seasons. Parameter stability was evaluated by comparing their CV with that of phenotype observation for the different sources of variability. A reduced data set was developed for easier model parameterization using one season, and validated for the four other seasons. The analysis of parameter stability among plants sharing the same environment and among populations grown in different environments indicated that the model explains some of the inter-seasonal variability of phenotype (parameters varied less than the phenotype itself), but not inter-plant variability (parameter and phenotype variability were similar). Parameter variability among developmental stages was small, indicating that parameter values were largely development-stage independent. The authors suggest that the high level of parameter stability observed in GREENLAB can be used to conduct comparisons among genotypes and, ultimately, genetic analyses.

The Legionella pneumophila Effector SidJ Is Required for Efficient Recruitment of Endoplasmic Reticulum Proteins to the Bacterial Phagosome

The virulence of Legionella pneumophila is dependent on the Dot/Icm type IV protein secretion system, which translocates effectors into infected cells. A large number of such translocated proteins have been identified, but few of these proteins are necessary for intracellular replication of the pathogen, making it difficult to correlate these genes with specific cell-biological events associated with L. pneumophila infection. We report here the identification and characterization of a family of two substrates, SidJ and SdjA, with distinctive phenotypes. In contrast to many Dot/Icm substrates, whose expression levels are elevated when bacteria are grown to postexponential phase, SidJ is produced at a constant rate during the entire bacterial growth cycle. Mutation in sidJ causes a significant growth defect in both macrophage and amoeba hosts, but an sdjA mutant is detectably defective only in protozoan hosts. However, in the amoeba host a mutant lacking both sidJ and sdjA does not display a more severe growth defect than the sidJ mutant. Despite its significant intracellular growth defect, the sidJ mutant is still able to effectively evade fusion with lysosomes. Importantly, recruitment of endoplasmic reticulum (ER) proteins by vacuoles containing the sidJ mutant was considerably delayed in both mammalian and amoeba cells. Our results suggest that SidJ modulates host cellular pathways, contributing to the trafficking or retention of ER-derived vesicles to L. pneumophila vacuoles.

The Secreted Protease Factor CPAF Is Responsible for Degrading Pro-apoptotic BH3-only Proteins in Chlamydia trachomatis-infected Cells

The Secreted Protease Factor CPAF Is Responsible for Degrading Pro-apoptotic BH3-only Proteins in Chlamydia trachomatis-infected Cells

The Hypothetical Protein CT813 Is Localized in theChlamydia trachomatisInclusion Membrane and Is Immunogenic in Women Urogenitally Infected withC. trachomatis

Using antibodies raised with chlamydial fusion proteins, we have localized a protein encoded by hypothetical open reading frame CT813 in the inclusion membrane of Chlamydia trachomatis. The detection of the C. trachomatis inclusion membrane by an anti-CT813 antibody was blocked by the CT813 protein but not unrelated fusion proteins. The CT813 protein was detected as early as 12 h after chlamydial infection and was present in the inclusion membrane during the entire growth cycle. All tested serovars from C. trachomatis but not other chlamydial species expressed the CT813 protein. Exogenously expressed CT813 protein in HeLa cells displayed a cytoskeleton-like structure similar to but not overlapping with host cell intermediate filaments, suggesting that the CT813 protein is able to either polymerize or associate with host cell cytoskeletal structures. Finally, women with C. trachomatis urogenital infection developed high titers of antibodies to the CT813 protein, demonstrating that the CT813 protein is not only expressed but also immunogenic during chlamydial infection in humans. In all, the CT813 protein is an inclusion membrane protein unique to C. trachomatis species and has the potential to interact with host cells and induce host immune responses during natural infection. Thus, the CT813 protein may represent an important candidate for understanding C. trachomatis pathogenesis and developing intervention and prevention strategies for controlling C. trachomatis infection.

Molecular analysis and organization of the sigmaB operon in Staphylococcus aureus.

The alternative sigma factor sigma(B) of Staphylococcus aureus controls the expression of a variety of genes, including virulence determinants and global regulators. Genetic manipulations and transcriptional start point (TSP) analyses showed that the sigB operon is transcribed from at least two differentially controlled promoters: a putative sigma(A)-dependent promoter, termed sigB(p1), giving rise to a 3.6-kb transcript covering sa2059-sa2058-rsbU-rsbV-rsbW-sigB, and a sigma(B)-dependent promoter, sigB(p3), initiating a 1.6-kb transcript covering rsbV-rsbW-sigB. TSP and promoter-reporter gene fusion experiments indicated that a third promoter, tentatively termed sigB(p2) and proposed to lead to a 2.5-kb transcript, including rsbU-rsbV-rsbW-sigB, might govern the expression of the sigB operon. Environmental stresses, such as heat shock and salt stress, induced a rapid response within minutes from promoters sigB(p1) and sigB(p3). In vitro, the sigB(p1) promoter was active in the early growth stages, while the sigB(p2) and sigB(p3) promoters produced transcripts throughout the growth cycle, with sigB(p3) peaking around the transition state between exponential growth and stationary phase. The amount of sigB transcripts, however, did not reflect the concentration of sigma(B) measured in cell extracts, which remained constant over the entire growth cycle. In a guinea pig cage model of infection, sigB transcripts were as abundant 2 and 8 days postinoculation as values found in vitro, demonstrating that sigB is indeed transcribed during the course of infection. Physical interactions between staphylococcal RsbU-RsbV, RsbV-RsbW, and RsbW-sigma(B) were inferred from a yeast (Saccharomyces cerevisiae) two-hybrid approach, indicating the presence of a partner-switching mechanism in the sigma(B) activation cascade similar to that of Bacillus subtilis. The finding that overexpression of RsbU was sufficient to trigger an immediate and strong activation of sigma(B), however, signals a relevant difference in the regulation of sigma(B) activation between B. subtilis and S. aureus in the cascade upstream of RsbU.

SigmaB activity in a Staphylococcus aureus hemB mutant.

Inactivation of hemB in Staphylococcus aureus strain Newman resulted in a small-colony phenotype and was accompanied by an altered expression pattern of global regulators and control of virulence factor production. Transcription profiles followed over 15 h by Northern blot analyses revealed that transcripts of the global regulators arl, rot, sae, sarR, sarS, srr, svrA, and sigB disappeared after the exponential phase and that both agr transcripts were completely absent in the hemB mutant. Apart from a general concentration of transcriptional activity to the exponential phase, premature gene expression was observed for rot, hla, and spa. Nevertheless, reported sigmaB-dependent transcripts, such as sarC and clfA, were produced throughout the 15-h growth period monitored. The absence of these transcripts in a hemB sigB double mutant demonstrated their dependence on sigmaB and indicated an unexpected, permanent sigmaB activity in the hemB mutant. Variations in the extents of the directly sigmaB-controlled asp23, rsbVW-sigB, and sarC transcripts argue for additional factors modulating sigmaB activity. This study provides the first extended synopsis of the transcriptional patterns of different regulators over the entire growth cycle in the widely used Newman strain.

Resource use efficiency of field-grown sunflower, sorghum, wheat and chickpea: I. Radiation use efficiency

Radiation use efficiency ( ɛ) is a crop parameter widely used in crop simulation models, derived here as the slope of the relationship linking crop carbon gain to cumulative intercepted solar radiation. Our objectives were to: (i) determine ɛ of field-grown sunflower, sorghum, wheat and chickpea, at three levels of aggregation—day-time net assimilation ( A), daily net carbon gain as difference between A and night-time dark respiration ( R) and biomass; (ii) assess the robustness of ɛ parameter in terms of ability to discriminate between C 3 and C 4 species, pre- and post-anthesis and impact of nitrogen status; (iii) evaluate the opportunity to normalize ɛ for climate. Field experiments were conducted in 1998 and 1999 in southern Italy. All crops were well watered. Sunflower and sorghum had two nitrogen application treatments, wheat only one and chickpea had no added nitrogen. Daily intercepted solar radiation was derived from measurements of daily incident solar radiation and the percentage of mid-day light interception. Closed-system canopy chambers monitored canopy gas-exchange rates. ɛ, expressed in terms of A, A − R or above-ground biomass, was linear over the entire growth cycle of sorghum and wheat, and up to anthesis in sunflower and chickpea, independent of temperature, vapour pressure deficit and radiation regimes. In sunflower, deviation from linearity was observed after anthesis, due to higher carbon cost in yielding oil seeds. No conclusions could be drawn for post-anthesis chickpea due to the interruption of the experiment caused by a thunderstorm. Overall results showed a great variability in ɛ values, independently of classes of species (C 4 and C 3), crops and nitrogen treatments. This indicates that the robustness of ɛ to predict biomass productivity in crop simulation models is constrained. Attempts to normalize ɛ by vapour pressure deficit ( D), for reducing its variability due to climate and overlaps between crops failed.

Growth Stage, Development, and Spatial Variability in Corn Evaluated Using Optical Sensor Readings*

ABSTRACT Knowing the exact stage of growth where expressed plant variability is at a maximum might lead to the identification of times when in-season fertilization could have the greatest impact. One field experiment was initiated to measure daily plant growth and spatial variability in corn (Zea mays L.) over the entire growth cycle using optical sensor readings (normalized difference vegetative index, or NDVI) collected every 0.05 m in length, 0.6 m wide from 4 corn rows, 27 m in length. Averaged over all 4 rows, plants were spaced 21 ± 7 cm apart. For each row and sensing date, the mean, standard deviation, and coefficient of variation (CV) were computed from the NDVI readings. Eighteen days after planting, NDVI values were near 0.20, and later peaked near 0.81, 54 days after planting at the 10-leaf growth stage (V10). Coefficients of variation were found to peak much earlier, 33 to 35 days after planting at the 6-leaf growth stage (V6), (31% to 34% during this period). Expressed spatial variability decreased from >30% at V6 to just under 10% at the 11-leaf growth stage (V11). Immediately following V11, a distinct increase in CVs was found just following the initiation of tasseling (VT), but lasted for only 2 days. Expressed spatial variability was greatest at the V6 growth stage, and this peak in the within-row-by-plant variability may be the precise growth stage at which treating that variability will have the greatest impact.

Culture performance of different strains and crosses of the European sea bass (Dicentrarchus labrax) reared under controlled conditions at Eilat, Israel

Summary The European sea bass (Dicentrarchus labrax) is one of the most important commercial marine fish species in the Mediterranean basin. However, broodstock domestication and selective breeding on a production scale have yet to be exploited. We reared progeny of sea bass from three different strains and their crosses throughout the entire growth cycle to market size. Data sets were analyzed to assess whether culture performance differs among different strains and crosses reared under controlled laboratory conditions using both separate and communal rearing techniques. Strains and crosses of sea bass varied significantly for traits of economic interest such as growth, survival, body composition, sex ratio, sexual maturation patterns of males, and frequencies of body shape abnormalities. Lack of evidence for substantial heterosis for growth among reciprocal crosses was also detected. Significant sexual dimorphism for length and weight was evident in all strains and crosses. At market size, the resulting weight advantages of females varied between strains and crosses; overall average weight advantage for females was about 39%. Length and weight of individual fish were strongly correlated during different time intervals. This may be useful for the choice of selection criteria, raising the possibility that the response to selection for weight at market time may be achieved by conducting selection on young fish. Generally, the results showed a high culture potential of sea bass strains originating from the southeastern areas of the Mediterranean Sea, suggesting that these domesticated strains can be exploited in future selective breeding programs.

Tracking Operator State Fluctuations in Gene Expression in Single Cells

We report the results of operator state fluctuations in gene expression for the entire bacterial growth cycle, using single-cell analysis and synthetic unregulated and negative-feedback transcription regulatory gene circuits. In the unregulated circuit, during the cell cycle, we observe a crossover from log-normal-to-normal distribution of expressed proteins and an unusual linear dependence of their standard deviation on the mean gene expression levels. With negative-feedback circuits we find the existence of bimodality as the cell cycle progresses. We suggest that such long-tail and bimodal distributions may be used as selection mechanisms in developmental switches and for assigning cell identity.