The effect of light and temperature on the growth and photosynthesis of Gracilariopsis chorda (Gracilariales, Rhodophtya) from geographically separated locations of Japan

The effect of light and temperature on the growth and photosynthesis of the Japanese agarophyte, Gracilariopsis chorda (Gracilariaceae, Rhodophyta), was determined to better understand its physiology so that we could identify candidates for mass cultivation. Above the photosynthetic active radiation of 66 μmol photons m^?2 s^?1, photosynthetic rates saturated for all strains that were collected from six different locations (Hokkaido, Chiba, Tokushima, Saga, Kagoshima, and Okinawa); furthermore, either photosynthesis or growth was observed at all temperature treatments examined in our study (4–32 °C for photosynthesis, 16–32 °C for growth experiments). We identified a temperature range for optimal photosynthesis and growth, which occurred within 20.1–29.1 °C and roughly correlated with the water temperatures of the collection locations and strongly suggests that this species tolerates a wide variety of water temperature. In particular, the Kagoshima strain had the widest range of optimal temperatures (20.8–29.1 °C), whereas the Saga strain had the narrowest range (23.1–27.3 °C). It is important to note that all the optimal temperature ranges overlapped among the strains; therefore, no definitive distinction can be determined. The broad tolerance to temperatures commonly observed from northern to southern Japan suggests that the cultivation of this species should succeed during spring to summer in the majority of the coastal regions in Japan.     

The effects of desiccation and salinity gradients on the PSII photochemical efficiency of an intertidal brown alga,Sargassum fusiforme from Kagoshima,Japan

The responses of photochemical efficiency to desiccation and salinity gradients in an intertidal edible brown macroalga, Sargassum fusiforme (Harvey) Setchell (Sargassaceae, Fucales), were determined using a pulse amplitude modulation (PAM)-chlorophyll fluorometer. The effective quantum yields (ΔF/F_m'; = Φ_PSII) of photosystem II (PSII) dropped to zero after 360-min aerial exposure under low irradiance (20 μmol photons m⁻² s⁻¹) and 120-min exposure under high irradiance (700 μmol photons m⁻² s⁻¹) for this species at 20°C and 50% relative humidity. Under these conditions, ΔF/F_m' failed to recover to initial levels even after 1-day rehydration in seawater. In general, ΔF/F_m' decreased as desiccation reduced the absolute water content (AWC, %). Nevertheless, when AWC was above ca. 20%, ΔF/F_m' was mostly restored to initial levels after 1-day rehydration in seawater, suggesting strong tolerance to dehydration. Furthermore, S. fusiforme appeared to tolerate a broad range of salinity (i.e. 15–50 psu) during six days of culture; however, ΔF/F_m' declined when salinity was <10 and 60 psu. Strong tolerance to dehydration and salinity stress likely provides S. fusiforme an advantage that allows it to flourish in the intertidal habitat.     

Effects of S-3307, an Inhibitor of Gibberellin Biosynthesis, on Swelling of Leaf Sheath Cells and on the Arrangement of Cortical Microtubules in Onion Seedlings

Treatment with S-3307, a newly developed growth retardant, causedswelling of leaf sheaths in 2- to 3-leafed young onion seedlings(Allium ccpa L. cv. Senshu-Chuko), which otherwise showed noswelling even under long-day conditions. Before swelling becameevident, changes occurred in the arrangement of cortical microtubulesin leaf sheath cells of S-3307-treated seedlings. Cortical microtubulesin leaf sheath cells, which are normally oriented transverselyto the cell axis in untreated seedlings, were oriented longitudinallyor obliquely in treated seedlings. S-3307 exerted these effectsonly in seedlings grown under long-day conditions, but not undershort-day conditions. Simultaneously applied gibberellin reversed the effect of S-3307on swelling, indicating that S-3307 acts as an inhibitor ofgibberellin biosynthesis in onion seedlings. Endogenous gibberellinseems to play an important role in arranging cortical microtubulestransversely to the cell axis. (Received July 14, 1984; Accepted September 26, 1984)     

Differential Expression of Genes Involved in the Biosynthesis and Perception of Ethylene during Ripening of Passion Fruit (Passiflora edulis Sims)

An increase in the enzyme activity of 1-aminocyclopropane-1-carboxylicacid (ACC) synthase and ACC oxidase induces the evolution ofethylene during the ripening of passion fruit. A much higherlevel of ethylene is produced in arils than in seeds or peelsduring ripening. The pattern of expression of two ACC synthasegenes (PE-ACS1 and PE-ACS2), one ACC oxidase gene (PE-ACO1),and two ethylene receptor genes (PE-ETR1 and PE-ERS1) revealedthat the expression of these genes is differentially regulated.Expression of PE-ACS1 and PE-ACO1 was enhanced during ripeningand after ethylene treatment. However, prominent expressionof PE-ACS1 was delayed compared to that of PE-ACO1. Much largerquantities of PE-ACS1 mRNA and PE-ACO1 mRNA were seen in arilsthan in seeds; this corresponds well with an increase in theamount of ethylene produced by the plant tissue itself. Thelevel of PE-ACS2 mRNA was detectable in arils of the preclimactericfruit, although it decreased during ripening. These resultssuggest that expression of PE-ACS1 and PE-ACO1 is required toincrease the activity of ethylene biosynthetic enzymes duringripening. The level of expression of PE-ETR1 and PE-ERS1 didnot significantly change over the course of ripening; however,the mRNA levels of PE-ETR1 and PE-ERS1 were much higher in arilsthan in seeds. ⁴Present address: Center forMolecular Genetics Research, Shizuoka University, Shizuoka, 422-8529 Japan.     

Isothermal and non-isothermal bioreactors in the detoxification of waste waters polluted by aromatic compounds by means of immobilised laccase from Rhus vernicifera

Laccase from Rhus vernicifera was immobilised on a nylon membrane chemically grafted with glycidyl methacrylate (GMA). Hexamethylenediamine (HMDA) and glutaraldehyde (GLU) were used as spacer and bifunctional coupling agent, respectively. Quinol was used as substrate.

To know how the immobilisation procedures affected the enzyme reaction rate the catalytic behaviour of soluble and insoluble laccase was studied under isothermal conditions as a function of pH, temperature and substrate concentration. From these studies, two main singularities emerged from the experimental data: (i) the narrower pH-activity profile of the insoluble enzyme in comparison to that of the soluble counterpart; (ii) the increase of the affinity of the immobilised enzyme for its substrate.

The behaviour of the catalytic membrane was also studied in a non-isothermal bioreactor as a function of substrate concentration and size of the applied transmembrane temperature difference. It was found that, under non-isothermal conditions and keeping constant the average temperature of the bioreactor, the enzyme reaction rate linearly increases with the increase of the temperature difference. These results have been discussed in the frame of reference of the process of thermodialysis driving thermodiffusive transmembrane substrate fluxes, which add to the diffusive ones.

The advantages of the catalytic process carried out under non-isothermal conditions have been thrown in relief through the evaluation of the reduction of the production times and of the percentage increases of the enzyme activity.     

Construction of scrA::lacZ gene fusions to investigate regulation of the sucrose PTS of Streptococcus mutans

The scrA gene coding for sucrose EnzymeII of the phosphoenolpyruvate dependent phosphotransferase system previously isolated from Streptococcus mutans was fused in vitro to the promoterless lacZ' gene to monitor the expression of the scrA gene. The scrA::lacZ gene fusion was introduced back into S. mutans GS-5IS3 by two independent transformation procedures involving either linear or plasmid DNA to produce both scrA and scrA+ mutants. These mutants should prove useful for analyzing the regulation of sucrose transport in S. mutans.     

A simple and sensitive method for determination of human urinary kallikrein activity (kininogenase activity), using human low molecular weight kininogen

Human low molecular weight kininogen was partially purified and applied to the measurement of human glandular kallikrein as a substrate. The prepared human low molecular weight kininogen did not contain any significant amounts of kinin generating or destroying enzymes. When ethanol was added to the assay tube to stop the enzyme reaction, the substrate was almost completely removed from the incubation solution. Moreover, less than 1.25% ethanol had no effect on the kinin radioimmunoassay. These data suggest that the measurement of generated kinin can be done directly after the addition of ethanol. In this assay system, control tubes were unnecessary since the small volume of the urine samples (0.5 to 2.0 nl) contained negligible amounts of endogenous kinin. In a comparison of the availability as a substrate for human urinary kallikrein among human, dog and bovine low molecular weight kininogens, the enzyme activity was 5 or 100 times as high in the human substrate as in the dog and bovine substrates, suggesting that a human substrate is best for the human enzyme. A significant correlation was found between our previous method using bovine substrate and this method for human urinary kallikrein activity. In both methods, urinary kallikrein excretions were significantly lower in patients with essential hypertension and higher in those with primary aldosteronism, respectively. This simple, specific and sensitive kininogenase assay system seems to be very useful for investigating the physiological or pathophysiological role of the renal kallikrein-kinin system in hypertensive and renal diseases.