Reproductive cycles and spawning periods of two Lessepsian siganid fishes on the Lebanese coast

A total of 1048 specimens of Siganus rivulatus and Siganus luridus were collected from the Batrun area of the Mediterranean Sea from January 1999 to August 2000. The sex-ratio in both species did not differ significantly from 1 : 1 between size classes or months. For S. rivulatus , the estimated mean length at first maturity ( L _T50) was 132·5 mm for males and 136·5 mm for females, and 139·0 and 142·0 mm, respectively, for male and female S. luridus . Spawning occurred in June in S. rivulatus and from May to July in S. luridus . High temperature in summer appeared to be a limiting factor in the gonadal development of both siganid species, which have reduced their breeding seasons on the Lebanese coast compared to their native Red Sea.     

Ecology of the acanthocephalan Sclerocollum rubrimaris Schmidt and Paperna, 1978 (Rhadinorhynchidae: Gorgorhynchinae) from wild populations of rabbitfish (genus Siganus) in the northern Red Sea

The abundance, host relationships and microhabitat of Sclerocollum rubrimaris Schmidt & Paperna. 1978 (Rhadinorhynchidae: Gorgorhynchinae) were investigated in wild populations of the herbivorous rabbitfish ( Siganus spp.) from the Gulf of Eilat, northern Red Sea. Siganus rivulatus (Forsskål, 1775) and S. argenteus (Quoy & Gaimard, 1825), judging by the high infection prevalences, are the primary definite hosts, whereas S. luridus (Ruppell, 1828) was only rarely infected and thus regarded as an accessory host. Overdispersion of S. rubrimaris suprapopu-lations was greatest in S. rivulatus. Juvenile worms occurred year-round, but enhanced recruitment was evident in both host populations between February and July. A high parasite abundance observed during spring (March-May) was correlated with an extensive period of pre-spawning algal grazing by the host fish. In S. rivulatus , parasite abundance increased with increasing host size, whereas in S. argenteus it was highest in young hosts, and decreased in larger fish. The variability of infection patterns in the three rabbitfish species probably stems not only from parasite specificity but also from the different habitats, feeding habits and diet preferences. Sclerocollum rubrimaris has a restricted host range and is not known to infect other herbivorous coral reef fish. The main region of attachment of S. rubrimaris is the anterior 5–25% of the gut in both S. rivulatus and S. argenteus , and the mean position of immature worms is significantly more posterior than that of sexually mature individuals.     

In vitro culture decreases the expression of TGF(beta), Hsp47 and type I procollagen and increases the expression of CTGF in avian tendon explants

Weight-bearing tendons in many species, including humans, chickens and horses, are prone to failure, in many cases without a discernible cause. The normal function of the tendon depends on the proper assembly of fibrils of type I collagen, the main structural component of the tendon. We studied the effect of in vitro culture, temperature (37 degrees C vs. 43 degrees C) and wounding on the expression of mRNAs for several collagen regulators, transforming growth factor beta (TGF(beta)), heat shock protein 47 (Hsp47) and connective tissue growth factor (CTGF), in chicken embryonic gastrocnemius tendon explants. The expression of mRNAs for TGF(beta) and Hsp47, a chaperone of collagen assembly, remained strong during the first day of in vitro culture, but then it decreased, slightly more at higher temperature. Additional injury in selected tendons had no significant effect on the levels of TGF(beta) and Hsp47 mRNAs. Likewise, the level of immunostained type I procollagen also decreased with the length of culture. The expression of CTGF gradually increased from 0 at the time of tendon removal with the duration of culture to strong after three days of culture when the expression of TGF(beta) and Hsp47 was low. We conclude that in vitro culture over the period of several days rather than an increase in temperature or additional wounding decreases the expression of TGF(beta), Hsp47 and type I procollagen and increases the expression of CTGF.     

Compensating in the wild: is flexible growth the key to early juvenile survival?

We explore the mechanisms underlying the survival of a cohort of a coral reef fish ( Pomacentrus amboinensis ) in the first month following settlement. To investigate the extent to which growth history immediately following settlement is linked to early survival, we tagged 900 fish the morning after settlement and recaptured the survivors (n=34) 30 days later. Otolith analysis showed that individuals that were larger at settlement preferentially survived the first month in benthic habitats. We also compared these survivors with conspecifics from the same cohort that were collected at settlement and then outgrown in two experimental feeding conditions to produce fast- and slow-growing fish. Comparison of the growth histories exhibited by the survivors to those of experimental conspecifics revealed that survivors exhibited relatively slow initial growth during their first few days on the reef, followed by a period of accelerated growth. We suggest that the flexibility in growth potential of young fish allows for the occurrence of periods of rapid (and compensatory) growth that might enhance post-settlement survival by attenuating the high risk of size-selective mortality.     

Intermediates in the assembly of ribosomes by a mutant of Escherichia coli.

Escherichia coli strain 15--28 is a mutant that accumulates ribonucleoprotein ('47 S') particles during exponential growth. These particles contain mature 23 S rRNA, but lack three of the proteins of the larger ribosomal subunit, to which they are a precursor. In organisms growing at 20 degrees C, assembly of 47 S particles involves three intermediates that contain precursor 23 S rRNA, one of which has the same sedimentation properties as 47 S particles. Assembly of 50 S ribosomal subunits in the parent strain is 'normal'. There are three intermediates; each contains precursor 23 S rRNA, and one cannot be distinguished from completed subunits by sedimentation. Synthesis of 30 S ribosomal subunits in parent and mutant strains is qualitatively similar, but quantitatively different. When growth is at 37 degrees C, assembly in the mutant alters. There are now two sequential precursors to 47 S particles. Both contain precursor 23 S rRNA; one has the same sedimentation coefficient as 47 S particles. In some respects, synthesis in the mutant proceeds as though 47 S particles, rather than 50 S ribosomal subunits, are the end-product of assembly.     

Induction and resuscitation of viable but nonculturable Salmonella enterica serovar typhimurium DT104

Salmonella enterica serovar Typhimurium DT104 11601 was tested for its ability to maintain viability in minimal, chemically defined solutions. Periodic monitoring of growth and survival in microcosms of different ion concentrations, maintained at various temperatures, showed a gradual decline in culturable organisms ( approximately 235 days) at 5 degrees C. Organisms maintained at a higher temperature (21 degrees C) showed continuous, equivalent CFU per milliliter ( approximately 10(6)) up to 400 days after inoculation. Fluorescence microscopy with Baclight revealed that nonculturable cells were actually viable, while observations with scanning electron microscopy showed that the cells had retained their structural integrity. Temperature upshift (56 degrees C +/- 0.5, 15 s) of the nonculturable organisms (5 degrees C) in Trypticase soy broth followed by immediate inoculation onto Trypticase soy agar (TSA) gave evidence of resuscitation. Interestingly, S. enterica serovar Typhimurium DT104 from the microcosms at either 5 degrees C (1 to 200 days) or 21 degrees C (1 to 250 days) did not show enhanced growth after intermittent inoculation onto catalase-supplemented TSA. Furthermore, cells from 21 degrees C microcosms exposed to oxidative and osmotic stress showed greater resistance to stresses over increasing times of exposure than did recently grown cells. It is possible that the exceptional survivability and resilience of this particular strain may in part reflect the growing importance of this multidrug-resistant organism, in general, as a cause of intestinal disease in humans. The fact that S. enterica serovar Typhimurium DT104 11601 is capable of modifying its physiological characteristics, including entry into and recovery from the viable but nonculturable state, suggests the overall possibility that S. enterica serovar Typhimurium DT104 may be able to respond uniquely to various adverse environmental conditions.     

Laboratory spawning, larval development, and metamorphosis of the limpets Lottia digitalis and Lottia asmi (Patellogastropoda, Lottiidae)

Abstract. This study describes and compares laboratory spawning, larval development, and metamorphosis in the patellogastropod limpets Lottia digitalis and Lottia asmi. Both species were dioecious and freely spawned their gametes, which were fertilized externally. Eggs from L. digitalis and L. asmi averaged 155 and 134 μm in diameter, respectively. Early cleavage patterns were typical of other patellogastropods. Swimming trochophore larvae had developed ∼ 15 hours after fertilization, and ultimately developed into lecithotrophic veliger larvae that reached metamorphic competence at 5.25–5.5 days after fertilization (13°C). Food particles were frequently visible in the gut of newly metamorphosed individuals one day after settlement, and adult shell growth was typically initiated within 2–4 days of settlement. Small egg size in L. asmi , relative to other eastern Pacific lottiids, may be directly related to the need for high fecundity in this small-bodied species; however, developmental information is available for relatively few lottiid species. Because broadcasting lottiids do not secure egg masses in safe microhabitats for development, this reproductive mode may have been conducive to their ecological radiation into novel habitats.     

中国对虾继饥饿后的补偿生长研

1999年7至8月份,在25.0±0.5℃条件下对中国对虾（湿重,1.454±0.150g）进行了不同时间的饥饿处理后再供食的恢复生长实验。对照组C连续饱食投喂32d;处理组S4、S8和S12分别饥饿4、8和12d后再饱食投喂28、24和20d。主要结果如下饥饿结束时各处理组的干重和湿重显著低于对照组（P<0.05）;实验结束时S4组和对照组间的干重和湿重差异不显著（P>0.05）,而S8和S12两组的干重和湿重仍显著低于对照组（P<0.05）;恢复生长后各处理组的湿重摄食率显著高于对照组（P<0.05）。实验结果表明,中国对虾继饥饿后再恢复喂食出现完全或部分补偿生长效应,且这种补偿生长效应主要是通过恢复生长阶段食欲增大,摄食水平提高实现的。     

Genetic and physiological alterations occurring in a yeast population continuously propagated at increasing temperatures with cell recycling

This work investigated the effects of increasing temperature from 30°C to 47°C on the physiological and genetic characteristics of Saccharomyces cerevisiae strain 63M after continuous fermentation with cell recycling in a system of five reactors in series. Steady state was attained at 30°C, and then the temperature of the system was raised so it ranged from 35°C in the last reactor to 43°C in the first reactor or feeding reactor with a 2°C difference between reactors. After 15 days at steady state, the temperature was raised from 37°C to 45°C for 25 days at steady state, then from 39°C to 47°C for 20 days at steady state. Starter strain 63M was a hybrid strain constructed to have a MAT a/α, LYS/lys, URA/ura genotype. This hybrid yeast showed vigorous growth on plates at 40°C, weak growth at 41°C, positive assimilation of melibiose, positive fermentation of galactose, raffinose and sucrose. Of 156 isolates obtained from this system at the end of the fermentation process, only 17.3% showed the same characteristics as starter strain 63M. Alterations in mating type reaction and in utilization of raffinose, melibiose, and sucrose were identified. Only 1.9% of the isolates lost the ability to grow at 40°C. Isolates showing requirements for lysine and uracil were also obtained. In addition, cell survival was observed at 39–47°C, but no isolates showing growth above 41°C were obtained.     

The biology of Dendropoma corallinaceum and Serpulorbis natalensis, two South African vermetid gastropods

D. corallinacewn forms sheet-like colonies at Mean Low Water (MLW) on exposed rocky shores: S. natalensis forms loose aggregations under stones below MLW in more sheltered situations. Both species released young from July— December. D. corallinaceun has single embryos in capsules brooded free in the mantle cavity; S. natalensis has 20–40 embryos per capsule, the latter being attached to the roof of the shell and hanging through a dorsal slit in the mantle. The morphology of the crawling young is similar in both species, resembling adult errant prosobranchs. D. corallinaceum has a stouter, more streamlined protoconch than S. natalensis correlated with the more turbulent water of its habitat. The crawling young secrete a sticky mucous trail for adhesion to the substratum. They are strongly photopositive until settlement. D. corallinaceum can settle within 24 hours but may delay settlement to 4–5 days if suitable substrata are absent. Metamorphosis is complete 2 days after settlement. D. corallinaceum prefer to settle on Lithothamnion which is easily eroded by the radula to provide a groove for rapid, firm attachments to the substratum. Both species feed from mucous nets, S. natalensis having a slower feeding rhythm commensurate with its larger size. Contiguous pairs of S. natalensis have synchronised feeding rhythms, probably to reduce mutual net robbing. Particles are also filtered out of suspension; many particles are rejected in the pseudofaeces but some are ingested. D. corallinaceum and S. natalensis have many similar ecologically equivalent species throughout the warm temperate and tropical seas of the world.     

The alien false limpet (Siphonaria pectinata) in the Bizerte channel (northern Tunisia): spawning,development and growth under laboratory conditions

Spawning, development and growth of Siphonaria pectinata in the laboratory were studied and described in detail during a one-year study period. Egg ribbons were observed in February, March, April, June, July, August and September, with a peak in number of ribbons per individual in July. On average, individuals laid 9.0 ± 5.1 egg ribbons at a spawning frequency of one egg ribbon day^?1. The number of eggs per ribbon ranged from 752 to 50,400 depending on ribbon length. Embryonic development studied in February (13–15 °C), April (15–17 °C) and July (25–27 °C), reached hatching within 8–16 days with average larval lengths of 76.7 ± 5.9, 83.0 ± 11.3 and 78.3 ± 9.0 μm, respectively. Massive mortality was registered a few days after hatching, with larval longevity depending on the study period. Larval settlement occurred within 36–38 days after hatching, but only in the spawn deposited in February. Larval growth was slow during the first three weeks (18–26 μm week^?1) and then accelerated until the sixth week (40–67 μm week^?1). The present study contributes knowledge on the spawning, development and growth of S. pectinata, an alien species recently spreading throughout the Tunisian coast.     

Characterization of two alkyl hydroperoxide reductase C homologs alkyl hydroperoxide reductase C_H1 and alkyl hydroperoxide reductase C_H2 in Bacillus subtilis

AIM: To identify alkyl hydroperoxide reductase subunit C(AhpC) homologs in Bacillus subtilis(B. subtilis) and to characterize their structural and biochemical properties. AhpC is responsible for the detoxification of reactive oxygen species in bacteria.METHODS: Two AhpC homologs(AhpC_H1 and AhpC_H2) were identified by searching the B. subtilis database; these were then cloned and expressed in Escherichia coli. AhpC mutants carrying substitutions of catalytically important Cys residues(C37S, C47 S, C166 S, C37/47 S, C37/166 S, C47/166 S, and C37/47/166 S for AhpC_H1; C52 S, C169 S, and C52/169 S for AhpC_H2) were obtained by site-directed mutagenesis and purified, and their structure-function relationship was analyzed. The B. subtilis ahp C genes were disrupted by the short flanking homology method, and the phenotypes of the resulting AhpC-deficient bacteria were examined.RESULTS: Comparative characterization of AhpC homologs indicates that AhpC_H1 contains an extra C37, which forms a disulfide bond with the peroxidatic C47, and behaves like an atypical 2-Cys AhpC, while AhpC_H2 functions like a typical 2-Cys AhpC. Tryptic digestion analysis demonstrated the presence of intramolecular Cys37-Cys47 linkage, which could be reduced by thioredoxin, resulting in the association of the dimer into higher-molecular-mass complexes. Peroxidase activity analysis of Cys→Ser mutants indicated that three Cys residues were involved in the catalysis. AhpC_H1 was resistant to inactivation by peroxide substrates, but had lower activity at physiological H2O2 concentrations compared to AhpC_H2, suggesting that in B. subtilis, the enzymes may be physiologically functional at different substrate concentrations. The exposure to organic peroxides induced AhpC_H1 expression, while AhpC_H1-deficient mutants exhibited growth retardation in the stationary phase, suggesting the role of AhpC_H1 as an antioxidant scavenger of lipid hydroperoxides and a stress-response factor in B. subtilis. CONCLUSION: AhpC_H1, a novel atypical 2-Cys AhpC, is functionally distinct from AhpC_H2, a typical 2-Cys AhpC.     

Characterization of spermatozoa and eggs of the rabbitfish

The spermatozoon of Siganus rivulatus is symmetrical in its longitudinal axis, has no acrosome, an almost spherical nucleus, a small mid-piece with six mitochondria, centrioles arranged at an acute angle to each other, no nuclear fossa, and a flagellum without fins. Sperm motility is reversibly inhibited in the seminal plasma, and in electrolyte and non-electrolyte solutions of 100 mosmol kg⁻¹ and activated by an increase in osmotic pressure. The sperm motility parameters remain constant for 5 min after activation, then motility starts to decrease and stops 25–30 min after activation. Osmolalities between 600 and 1100 mosmol kg⁻¹ and a pH between 7·5 and 9·0 do not affect the sperm motility parameters. The eggs of S. rivulatus contain several large central lipid droplets composed of neutral lipids and glycolipids. Glycogen granules and sialoglycoproteins are dispersed between the lipid droplets. The protein yolk, consisting of neutral and slightly basic proteins is located peripherally. The cortical alveoli containing neutral polysaccharids are located in the outermost regions in close vicinity to the oolemma. The chorion is two-layered and has no specialized surface structures.     

Linking larval history to juvenile demography in the bicolor damselfish Stegastes partitus (Perciformes: Pomacentridae)

Otolith-based reconstructions of daily larval growth increments were used to examine the effect of variation in larval growth on size and age at settlement and post-settlement growth, survival and habitat preferences of juvenile bicolor damselfish (Stegastes partitus Poey). During August 1992 and 1994, newly settled S. partitus were collected from Montastraea coral heads and Porites rubble piles in Tague Bay, St. Croix, U.S. Virgin Islands (17 degrees 45'N, 64 degres 42' W). Daily lapillar otolith increments from each fish were counted and measured with Optimas image analysis software. S. partitus pelagic larval duration was 23.7 d in 1992 (n = 70) and 24.6 d in 1994 (n = 38) and larval age at settlement averaged 13.0 mm total length both years. Analysis of daily otolith increments demonstrated that variation in larval growth rates and size and age at settlement had no detectable effect on post-settlement survivorship but that larger larvae showed a preference for Montastraea coral at settlement. Late larval and early juvenile growth rates showed a significant positive relationship indicating that growth patterns established during the planktonic stage can span metamorphosis and continue into the benthic juvenile phase. Larval growth rates during the first two weeks post-hatching also had a strong effect on age to developmental competence (ability to undergo metamorphosis) in both 1992 and 1994 with the fastest growing larvae being 8 d younger and 0.8 mm smaller at settlement than the slowest growing larvae. These differential growth rates in early stage larvae established trajectories toward larval developmental competence and may prove important in biogeographical studies of larval dispersal.     

Growth and reduction of microorganisms in sediments collected from a greywater treatment system

AIMS: To study the effects of competitive microbiota, temperature and nutrient availability on Salmonella, Enterococcus, Campylobacter spores of sulphite reducing anaerobes and bacteriophages MS2 and phiX174 in sediments from a greywater treatment system. METHODS AND RESULTS: Standard culture methods were used. Bacteria died off rapidly under normal conditions (20 degrees C, competitive microbiota) but remained stable or grew in the other conditions studied. When the sediments became nutrient depleted after 2 weeks, a log-linear die-off was observed for Salmonella, which was higher at 20 degrees C than at 4 degrees C. Bacteriophage decay was shown to be log-linear from day 0, with T90 values ranging from 9 (phiX174, 20 degrees C) to 55 days (phiX174, 4 degrees C). The MS2 phage had a significantly higher decay rate in tyndallized sediments (T90 = 17 days) than in original sediments (T90 = 47 days) (P < 0.001), with temperature not shown to affect the decay rate. Spores of sulphite-reducing anaerobes were not significantly reduced during the study period (35 days). Campylobacter died-off rapidly or entered a viable but non-culturable state and subsequently results were not provided. CONCLUSIONS: Competition was the most important factor to suppress pathogenic bacterial growth in an eutrophic environment. When nutrient depleted conditions prevailed, temperature was more important and log-linear decay of microorganisms could be observed. SIGNIFICANCE AND IMPACT OF THE STUDY: These findings suggest that the normally occurring microbiota will suppress pathogenic bacterial growth in nutrient rich sediments. With lower nutrient status, temperature is the more important factor in reducing pathogens.     

Survival and growth of Salmonella Enteritidis PT 30 in almond orchard soils

Aims:  To evaluate factors potentially contributing to the long-term persistence of Salmonella enterica serovar Enteritidis phage type (PT) 30 in an almond orchard. Methods and Results:  Surface and subsurface soil temperatures, and air temperatures in a radiation shelter, were recorded during a 12-month period, and were used to identify relevant storage temperatures (20 or 35°C) for microcosms of two different soil types (clay and sandy loams) with moisture levels near saturation or near field capacity. Salmonella Enteritidis PT 30 was inoculated into the microcosms at 6 log CFU g⁻¹ dry weight. Between 14 and 180 days of incubation, counts of S. Enteritidis PT 30 decreased rapidly at 35°C and were significantly different (P < 0·05) from counts at 20°C, regardless of the soil type or moisture level. Salmonella was detected by enrichment of 10-g samples from all microcosms after 180 days of incubation at 20°C, but from none of the microcosms held at 35°C. To measure the potential for the growth of S. Enteritidis PT 30 in clay loam soil, an aqueous extract of almond hulls (containing 1·6% mono and disaccharides) or equivalent volume of water was added 7 days after inoculation. Significant (P < 0·05) growth of S. Enteritidis PT 30 was observed within 8 or 24 h of adding hull extract, but not water, to soil. Conclusions:  Opportunities may exist for S. Enteritidis PT 30 to survive for an extended time in almond orchard soils and to grow in these soils where hull nutrients are released. Significance and Impact of the Study:  Temperature has a significant impact on the long-term survival of S. Enteritidis PT 30 in soil, and nutrients leached from almond hulls may result in Salmonella growth. These factors should be considered in the design of Good Agricultural Practices for almonds.     

Induction and Resuscitation of Viable but Nonculturable Salmonella enterica Serovar Typhimurium DT104†

Salmonella enterica serovar Typhimurium DT104 11601was tested for its ability to maintain viability in minimal, chemically defined solutions. Periodic monitoring of growth and survival in microcosms of different ion concentrations, maintained at various temperatures, showed a gradual decline in culturable organisms (~235 days) at 5°C. Organisms maintained at a higher temperature (21°C) showed continuous, equivalent CFU per milliliter (~10⁶) up to 400 days after inoculation. Fluorescence microscopy with Baclight revealed that nonculturable cells were actually viable, while observations with scanning electron microscopy showed that the cells had retained their structural integrity. Temperature upshift (56°C ± 0.5, 15 s) of the nonculturable organisms (5°C) in Trypticase soy broth followed by immediate inoculation onto Trypticase soy agar (TSA) gave evidence of resuscitation. Interestingly, S. enterica serovar Typhimurium DT104 from the microcosms at either 5°C (1 to 200 days) or 21°C (1 to 250 days) did not show enhanced growth after intermittent inoculation onto catalase-supplemented TSA. Furthermore, cells from 21°C microcosms exposed to oxidative and osmotic stress showed greater resistance to stresses over increasing times of exposure than did recently grown cells. It is possible that the exceptional survivability and resilience of this particular strain may in part reflect the growing importance of this multidrug-resistant organism, in general, as a cause of intestinal disease in humans. The fact that S. enterica serovar Typhimurium DT104 11601 is capable of modifying its physiological characteristics, including entry into and recovery from the viable but nonculturable state, suggests the overall possibility that S. enterica serovar Typhimurium DT104 may be able to respond uniquely to various adverse environmental conditions.     

Release of ferulic acid and feruloylated oligosaccharides from sugar beet pulp by Streptomyces tendae

Given several promising industrial applications of ferulic acid, this study was designed to identify actinomycete strains able to release high levels of this acid from sugar beet pulp (SBP). Out of 47 strains tested, 37% were found to release free ferulic acid from the growth substrate. One strain, identified as Streptomyces tendae by 16S RNA gene sequencing, was capable of releasing 80% of the ferulic acid ester-linked to the pectin in SBP after 5 days of growth. These data suggest that some actinomycetes are able to release ferulic acid and feruloylated oligosaccharides from SBP. During growth on SBP, it seems that Streptomyces species solubilize and release feruloylated oligosaccharides by specific carbohydrase activities before de-esterification and release of free ferulic acid.     

Regulation mechanism of ERM (ezrin/radixin/moesin) protein/plasma membrane association: possible involvement of phosphatidylinositol turnover and Rho-dependent signaling pathway

Candida boidinii Pmp47, an integral peroxisomal membrane protein, belongs to a family of mitochondrial solute transporters (e.g., ATP/ADP exchanger), and is the only known peroxisomal member of this family. However, its physiological and biochemical functions have been unrevealed because of the difficulties in the molecular genetics of C. boidinii. In this study, we first isolated the PMP47 gene, which was the single gene encoding for Pmp47 in a gene-engineerable strain S2 of C. boidinii. Sequence analysis revealed that it was very similar to PMP47A and PMP47B genes from a polyploidal C. Boidinii strain (ATCC32195). Next, the PMP47 gene was disrupted and the disruption strain (pmp47delta) was analyzed. Depletion of PMP47 from strain S2 resulted in a retarded growth on oleate and a complete loss of growth on methanol. Both growth substrates require peroxisomal metabolism. EM observations revealed the presence of peroxisomes in methanol- and oleate-induced cells of pmp47delta, but in reduced numbers, and the presence of material of high electron density in the cytoplasm in both cases. Methanol-induced cells of pmp47delta were investigated in detail. The activity of one of the methanol-induced peroxisome matrix enzymes, dihydroxyacetone synthase (DHAS), was not detected in pmp47delta. Further biochemical and immunocytochemical experiments revealed that the DHAS protein aggregated in the cytoplasm as an inclusion body, while two other peroxisome matrix enzymes, alcohol oxidase (AOD) and catalase, were active and found in peroxisomes. Two peroxisome-deficient mutants, strains M6 and M13 (described in previous studies), retained DHAS activity although it was mislocalized to the cytoplasm and the nucleus. We disrupted PMP47 in these peroxisome- deficient mutants. In both strains, M6-pmp47delta and M13-pmp47delta, DHAS was enzymatically active and was located in the cytoplasm and the nucleus. We suggest that an unknown small molecule, which PMP47 transports, is necessary for the folding or the translocation machinery of DHAS within peroxisomes. Pmp47 does not catalyze folding directly because active DHAS is observed in the M6-pmp47delta and M13-pmp47delta strains. Since both AOD and DHAS have the PTS1 motif sequences at their carboxyl terminal, our results first show that depletion of Pmp47 could dissect the peroxisomal import pathway (PTS1 pathway) of these proteins.     

Thermophysiology of Streptococcus mutans and related lactic-acid bacteria

The temperature ranges for growth of Streptococcus mutans GS-5 and S. sobrinus 6715 were found to be very narrow, from about 30 to 47 °C, with optimal growth around 37 °C. Thus, the organisms showed little potential to grow in the environment outside of the animal host. In contrast wider ranges were found for Enterococcus hirae, S. rattus and S. sanguis. Detailed study of S. mutans GS-5 showed that energetic coupling, reflected in yields of biomass per mol of glucose utilized, were not greatly affected by changes in temperature within the growth range. However, since glycolysis occurred over a wider temperature range (about 10 to 52 °C) than growth, yield values dropped to zero at temperatures above or below the growth range. The temperature range for glycolysis could be related to temperature sensitivity of the phosphoenolpyruvate: sugar phosphotransferase system for sugar uptake. F-ATPases were active over a similar range of temperatures, but with a broad optimal range from about 30 to 50 °C. Proton permeability of S. mutans increased steadily with temperature in a manner similar to that of other mesophilic bacteria, such as Escherichia coli. Growth of the bacteria in media supplemented with various fatty acids had major effects on proton permeabilities but the effects were not well reflected by changes in growth or glycolysis of the bacteria. The overall conclusions were that S. mutans is a typical mesophile in relation to membrane and catabolic functions but its narrow temperature range for growth is related to temperature sensitivities of anabolic systems.