Purification and kinetics of extracellular phospholipase a ofSalmonella newport

Attempts were made to purify and study the kinetics of extracellular phospholipase A of Salmonella newport (6,8, eb; 1,2). The enzyme was purified by salt precipitation followed by gel filtration, using different grades of Sephadex. The enzymically active purified preparation was found to be a protein, having molar mass ranging between 43 and 67 kDa. The enzyme had a pH optimum at 7.5, giving 18.2 micrograms of lysophosphatidylcholine per mg protein. Its activity was enhanced by all metal ions except potassium, by solvents and surfactants except sodium dodecyl sulfate. It hydrolyzed the membrane phospholipids of red blood cells and was inhibitory to the growth of other microorganisms.     

Factors affecting production and activity of phospholipase C by Yersinia enterocolitica

The production of phospholipase C by Yersinia enterocolitica strain SG was optimum at 37 degrees C at pH 6.5. No enzyme activity could be detected when the organism was grown at extreme pH values (pH greater than 8.5 or less than 5.0). The enzyme production was maximum when the organism was grown under static conditions in TSB medium. All solvents and salts inhibited the enzyme activity, whereas loss of activity was 95% in presence of methanol (20%) and 99% in presence of sodium azide (0.2 mol/l). The enzyme activity was increased twofold in the presence of cysteine and decreased by 98% in the presence of sodium perchlorate (0.2 mol/l).     

Factors affecting production and activity of phospholipase C by Yersinia enterocotttica

The production of phospholipase C by Yersinia enterocolitica strain SG was optimum at 37†C at pH 6·5. No enzyme activity could be detected when the organism was grown at extreme pH values (pH > 8·5 or <5·0). The enzyme production was maximum when the organism was grown under static conditions in TSB medium. All solvents and salts inhibited the enzyme activity, whereas loss of activity was 95% in presence of methanol (20%) and 99% in presence of sodium azide (0·2 mol/l). The enzyme activity was increased twofold in the presence of cyste-ine and decreased by 98% in the presence of sodium perchlorate (0·2 mol/1).     

Structural and functional changes in rabbit ileum by purified extracellular phospholipase a ofSalmonella newport

As phospholipases ofSalmonella species may play a role in the pathogenesis of gastrointestinal tract diseases.Salmonella newport, the causative agent of infantile diarrhoea was examined for the production of phospholipase. The enzyme was purified by gel filtration chromatography and was found to be a protein of molar mass ranging from 43 to 67 kDa. The purified enzyme alone or in combination with organisms, produced both structural and functional changes in rabbit ileum, contributing towards pathogenesis of diarrhoea due to this organism.     

A sucrose-inducible promoter system for the intra- and extracellular protein production in Bacillus megaterium

A sucrose-inducible promoter system (P(sacB)) from Bacillus megaterium was identified using a secretome approach. It was successfully employed for the extracellular production of the homologous levansucrase SacB (4252.4 U l(-1)) and the heterologous green fluorescent protein GFP (7.9 mg g(CDW)(-1)). Mutational analysis of B. megaterium P(sacB) allowed the identification of important promoter elements. The sucrose-inducible promoter provides a useful alternative to the established xylose-inducible promoter system (P(xylA)) for recombinant gene expression in B. megaterium.     

Factors affecting goat milk production and quality

Differences between production systems based on grazing and browsing vs. use of harvested feedstuffs in confinement largely depend on specific feedstuffs and plants available and being consumed. Low forage nutrient ingestion should have relatively greater impact on tissue mobilization than milk production in early than later periods of lactation, with a transition to proportionally greater change in milk production in late lactation. However, low body condition at kidding would limit tissue energy mobilization and restrict impact of level of nutrient intake to milk yield and, likewise, tissue mobilization would be less with one vs. two or three milkings per day. As lactation advances after freshening, fat and protein levels decrease with increasing milk yield, and when production declines in mid- to late lactation, fat and protein concentrations increase. Milk production generally peaks at a parity of 3 or 4, thereafter declining slowly. Elevated somatic cell count alone in dairy goats is not a valid indication of mammary infection. Extended lactations offer opportunities to minimize or avoid seasonal fluctuations in milk production and lessen production costs. If differences in performance between suckled and machine-milked dairy goats occur, they may be restricted to or of greater magnitude during the suckling period compared with post-weaning, and differences in milk yield will either be absent or less with one kid compared with greater litter sizes. The magnitude of effects of milking frequency on milk yield is less for goats of low vs. high production potential and with low vs. high diet quality. Likewise, the effect of milking frequency is greater in early and mid-lactation when yield is higher than in late lactation, along with a shorter period of peak production with one vs. two daily milkings. Physical form of the diet can affect production and composition of goat milk, although effects appear of smaller magnitude than in dairy cattle. When tissue is mobilized to support milk production in early lactation, levels of C18:0 and C18:1 cis in milk increase and levels of medium-chain fatty acids decline. Effects of elevated levels of dietary fatty acids on specific long-chain fatty acids in milk and milk products vary with the fatty acid profile of fat sources used.     

Factors affecting hemolysin production byVibrio vulnificus

Factors affecting the hemolytic activity ofVibrio vulnificus cultures supernatant fluids against sheep erythrocytes were studied in order to optimize conditions and develop an assay system to assess the pathogenic potential of marineV. vulnificus strains. The heat-labile hemolysin produced during logarithmic growth ofV. vulnificus was produced optimally in heart infusion broth (HIB). Lesser amounts of hemolysin were produced in brain-heart infusion and tryptic soy broths. Hemolytic activity of HIB cultures decreased with increasing NaCl concentrations. Higher NaCl concentrations were found to affect hemolysin production but not its activity. The assay system described herein is a simple and rapid method that is being applied to the study of the pathogenic potential ofV. vulnificus strains from marine environments.     

同源四倍体水稻原种制备及影响因素分析

本研究已将从全国各地征集的50份水稻优良种质资源(2n=2x=24)诱变为同源四倍体水稻原种。本文讨论不同处理日期、不同秋水仙碱浓度和处理时间、以及不同品种的抗药性等因素对加倍成功率的影响,结果表明:①不同日期处理水稻幼芽,其加倍成功率不同,4月6日～15日加倍效果最好,加倍成功率达19.4%。②不同浓度秋水仙碱和处理时间其加倍成功率存在一定的差别。0.1%秋水仙碱处理48h 和0.2%处理24h 为佳,其芽恢复率超过58%,加倍成功率超过16%。③不同水稻品种抗药性不同。在所加倍的50个水稻品种中,中作9025抗药性最强,芽恢复率达92.4%,加倍成功率38.7%。盐州14抗药性最差,芽恢复率仅为10.6%。     

Factors affecting pheromone production in beetles

Pheromone production and/or release by beetles is coordinated with a variety of behavioral, physiological, and environmental factors. To data, two basic mechanisms for the regulation of pheromone biosynthesis in beetles have been proposed. Pheromone biosynthesis may simply be dependent on the availability of biosynthetic precursors. Alternatively, certain stimuli or events may trigger pheromone biosynthesis via juvenile hormone (JH) action. JH may either act directly at the site of pheromone biosynthesis to enhance pheromone production or may act indirectly, through a brain hormone (which might be related to the pheromone biosynthesis activating neuropeptide) or through effects on antennal sensory response. Knowledge of the regulation of the initiation and termination of pheromone biosynthesis is reviewed. Mechanisms by which pheromone stereochemistry is controlled are also discussed. This is an important aspect of pheromone production in Coleoptera, since slight changes in the stereochemistry can completely alter the activity of the molecule. © 1994 Wiley-Liss, Inc.     

Factors affecting the phospholipase activity of Candida species in vitro

The phospholipase activity of 41 isolates of oral Candida species was determined by a plate assay. Seventy nine per cent of the C. albicans isolates were phospholipase producers whereas none of the C. tropicalis, C. glabrata or C. parapsilosis isolates produced the enzyme. The degree of phospholipase activity (Pz value) of individual isolates was remarkably constant despite the large variation in activity among different isolates. Experiments with 10 phospholipase positive C. albicans isolates indicate that phospholipase production in vitro is limited to a narrow pH range (c. 3.6-4.7) and is suppressed by increasing concentrations of sucrose and galactose in the media (r = 0.9). Hence, candidal phospholipases seem to play a complex role in the aetiopathology of human candidoses.     

Interplay between intra- and extracellular calcium ions

Two, well characterized cationic channels, the ryanodine receptor (RyR) and the canonical transient receptor potential cation channel (TRPC) are briefly reviewed with a particular attention on recent developments related to the interplay between the two channel families.     

Factors affecting the production of pyrroloquinoline quinone by the methylotrophic bacterium W3A1

Two variants of the methylotrophic bacterium W3A1, designated W3A1-S (slimy) and W3A1-NS (nonslimy), were compared with respect to their ability to grow in batch culture on the C1 substrates methylamine, methanol, and trimethylamine. Substrate utilization, cell density, pH, cellular and soluble polysaccharide production, and concentrations of the enzymes methylamine dehydrogenase, trimethylamine dehydrogenase, and methanol dehydrogenase produced were measured as a function of growth. The ability of the two bacterial variants to excrete the redox cofactor pyrroloquinoline quinone into the growth medium was also investigated. The two variants were similar with respect to all properties measured, except that W3A1-S produced significantly more capsular polysaccharides than variant W3A1-NS. Pyrroloquinoline quinone was excreted when either variant was grown on any of the C1 substrates investigated but was maximally produced when the methylamine concentration was 0.45% (wt/vol). This cofactor is excreted only as bacterial growth enters the stationary phase, a time when the levels of trimethylamine dehydrogenase and the quinoproteins methanol dehydrogenase and methylamine dehydrogenase begin to decline. It is not known whether the pyrroloquinoline quinone found in the medium is made de novo for excretion, derived from the quinoprotein pool, or both. Pyrroloquinoline quinone excretion has been observed with other methylotrophs, but this is the first instance where the excretion was observed with substrates other than methanol.     

Factors affecting laboratory production of buffalo embryos: A meta-analysis

In vitro fertilization (IVF) provides an excellent and inexpensive source of embryos for carrying out basic research on developmental physiology, farm animal breeding, and for commercial applications. Meta-analysis of the results from different publications rather than a narrative review may provide a current status of this technology in buffalo (Bubalus bubalis). In order to gain an idea of the factors affecting the IVF in buffalo, a review of the various studies conducted on buffalo IVF and a meta-analysis of their findings was undertaken. More than 100 articles published from 1991 to 2008 were searched, and results were subjected to meta-analysis to determine the treatment variations without any bias. Thirty factors affecting in vitro embryo production in buffalo were considered. Initially, both fixed- and random-effect models were used. We did not observe any heterogeneity between the studies. Thereafter, all the studies were pooled using the fixed-effect model for analysis. Our analysis suggested that good buffalo oocytes with more than three to five cumulus layers recovered from large-sized follicles in cold seasons when cultured in TCM-199 supplemented with serum, follicle-stimulating hormone, and cysteamine resulted in maximum maturation rate and subsequent embryonic development after insemination. The values obtained in the current study may be considered for a simulation model in establishing a cost-effective suitable method for buffalo IVF in further planned research.     

Influence of intra- and extracellular sucrases of Zymomonas mobilison the ethanol production and by-product formation

A spontaneous mutant of Zymomonas mobilis LS1A lacking intracellular sucrase SacA was isolated from a levan-sucrase mutant of Z. mobilis LS1. The intracellular sucrase SacA does not have a role in sucrose hydrolysis and fermentation. The amount of the extracellular levansucrase SacB produced by the strain B-806 was about one third of the total sucrase activity. In the absence of the SacB, the strains LS1 and LS1A did not produce levan during sucrose fermentation. The extracellular sucrase SacC was sufficient for the complete hydrolysis of sucrose for fermen-tation. The low hydrolysis rate of sucrose was responsible for the increased amount of ethanol production (37.5 g/l to 44.2 g/l) and the decreased amount of sorbitol production (4.5 g/l to 1.2 g/l) by the strains LS1 and LS1A.     

Novel plasmid-based expression vectors for intra- and extracellular production of recombinant proteins in Bacillus subtilis

Two plasmid-based expression vectors have been constructed where one allows intracellular production of recombinant proteins while the second directs the proteins into the culture medium. Both vectors use the strong promoter preceding the groESL operon (codes for the essential heat shock proteins GroES and GroEL) of Bacillus subtilis fused to the lac operator allowing their induction by addition of ITPG. While the background level of expression of these expression cassettes is very low in the absence of the inducer, an induction factor of about 1300 was measured. When the genes htpG and pbpE (coding for a heat shock protein and a penicillin-binding protein, respectively) were fused to the groE promoter, the amount of recombinant protein produced after addition of IPTG represented 10 and 13%, respectively, of the total cellular protein. To obtain secretion of recombinant proteins, the coding region for the signal peptide of the amyQ gene encoding an alpha-amylase from Bacillus amyloliquefasciens was fused to the groE promoter. High-level secretion of amyQ alpha-amylase and cellulase A and B of Clostridium thermocellum was demonstrated.     

Controlled intra- or extracellular production of staphylococcal nuclease and ovine omega interferon in Lactococcus lactis

A system for controlled targeting of heterologous protein was developed in the food-grade bacterium Lactococcus lactis. It is composed of the L. lactis strain NZ9000 and of two broad host range expression vectors pCYT:Nuc and pSEC:Nuc for, respectively, cytoplasmic and secreted staphylococcal nuclease (Nuc) nisin-inducible production. The level of intracellular production of Nuc measured with pCYT:Nuc (3 mg x l(-1)) is significantly lower than the one obtained with pSEC:Nuc ( approximately 20 mg x l(-1)). The secretion efficiency (SE) of Nuc is estimated to be approximately 70%, corresponding to approximately 15 mg of secreted Nuc x l(-1). Furthermore, we established that Nuc production continued in L. lactis 10 h after a 1-h nisin-pulse induction. This system was then used for intra- and extracellular production of a protein of therapeutical interest in L. lactis, the ovine interferon-omega (IFN-omega). The SE and the quantity of secreted active IFN-omega were evaluated respectively to be approximately 70% and approximately 1 mg x l(-1) ( approximately two-fold higher than the cytoplasmic form).     

Factors affecting progeny production of Anaphes iole

Anaphes iole Girault(Hymenoptera: Mymaridae) is a native, solitaryegg parasitoid of Lygus spp.(Heteroptera: Miridae) in North America. Current research is considering factors thatmay optimize the in-vivo rearing of A.iole using Lygus hesperus Knight(Heteroptera: Miridae) as host. The effects ofhost density, day of oviposition and foodpresence, parasitoid age and mate presence onproduction of A. iole progeny weredetermined in this study. After exposingindividual parasitoids to host patches for 24h, the percentage of hosts containing a latestage A. iole pupa wassignificantly greater at a moderate hostdensity (41–70 eggs per patch) than at a lowdensity (10–40 eggs). But, no differenceswere detected between moderate and high density(71–100 eggs) or between high and low densitytreatments. More adult progeny were generatedby females (of variable age; 0–2 d old) onthe first day of oviposition rather than thesecond day, regardless of food presence. Progeny sex ratio was decidedly male-biased onthe second day. Female age (0 d vs 1 d old)had a marginal effect on production in 24 h; 0d old females tended to generate more adultprogeny than 1 d old females. Overall, thisresearch suggests that exposing newly-emerged,unfed, mated A. iole females to amoderate to high host density for 1 to 2 dcould lead to time-efficient production ofadult progeny in an in-vivo rearing system.