Isolation of an aboriginal bacterial community capable of utilizing cyanide, thiocyanate, and ammonia from metallurgical plant wastewater

An aboriginal bacterial community capable of degrading cyanide (10 mg/l) and thiocyanate (2 g/l) and eliminating ammonia (120 mg/l) had been isolated from recycled water samples after blast-furnace gas purification of a metallurgical plant wastewater. It was shown that the optimal conditions for this bacterial community were as follows: temperature, 34 degrees C; pH, 8.8-9.0; available organic matter concentration (glucose equivalent), 5 g/l; and dissolved O2 concentration, 8-10 mg/l. This aboriginal community was formed by the bacteria belonging to the genus Pseudomonas.     

Development of an Oil-Degrading Biopreparation by Activation of Aboriginal Hydrocarbon-Oxidizing Microflora

A method of activation of aboriginal hydrocarbon-oxidizing microorganisms for remediation of soil and water basins polluted with oil products was developed. The optimum composition of activating additives was found (g/l): mineral components, 10.0; oil, 5.0; and a synthetic detergent, 0.2. The resulting biopreparations increased the degree of purification by factors of 4–8 in soil and 18–24 in water when applied at a concentration of 10⁷ cells/g(ml).     

Some physical,chemical, and microbiological characteristics of two beaches of anglesey

Observations during 1971 and 1972 of some of the physical, chemical, and microbiological characteristics of contrasting Anglesey beaches, Newborough and Llanddona, are reported. The fine sandy beach at Newborough was observed to be very unstable and topographical changes were recorded. In particular, the movement of a sand wave across the intertidal zone from low water to extinction at the foot of the dune system was observed. The more extensive fine sandy beach at Llanddona had greater stability.Chemically, each beach was variable both spatially and temporally, with ill-defined patterns of concentration changes. Sand from Newborough beach was low in organic carbon (0.07–0.40 mg C/g dry sand) and well aerated, and the soluble inorganic nitrogen in the ground water (up to 30 μg-at. N/l) was dominated by nitrate form (up to 22 μg NO₃-N/l). By contrast, Llanddona sand had a more variable organic carbon content (0.22–2.25 mg C/g dry sand), was wetter, and poorly aerated with consequent sulphide lenses; its dissolved inorganic nitrogen (over 70 μg-at. N/l) was completely dominated by the ammonium form.Microbiologically, the beaches possessed dissimilar bacterial floras, and sediment from Llanddona gave higher bacterial counts than that from Newborough. For both beaches it is shown that estimated bacterial numbers decreased with depth as well as down the intertidal zone.     

Effects of dissolved oxygen concentration and DO-stat feeding strategy on CoQ10 production with Rhizobium radiobacter

The cell growth and CoQ₁₀ (coenzyme Q₁₀) formation of Rhizobium radiobacter WSH2601 were investigated in a 7-1 bioreactor under different dissolved oxygen (DO) concentrations. A maximal CoQ₁₀ content (C/B) of 1.91 mg/g dry cell weight (DCW) and CoQ₁₀ concentration of 32.1 mg/l were obtained at the appropriate DO concentration of 40% (of air saturation). High DO concentration was favourable to the cell growth of Rhizobium radiobacter WSH2601. In order to achieve the maximal yield of CoQ₁₀ production, a new DO-stat feeding strategy was proposed, which significantly improved cell growth and CoQ₁₀ formation. With this strategy, the maximal CoQ₁₀ concentration and DCW reached 51.1 mg/l and 23.9 g/l, respectively, which were 67 and 44.8% higher than those obtained in the batch culture with DO concentration controlled.     

Effect of basal medium, growth regulators and Phytagel concentration on initiation of embryogenic cultures from immature zygotic embryos of loblolly pine (Pinus taeda L.)

Low initiation frequency is one of the main barriers in applying somatic embryogenesis to the clonal production of Pinus species. Factors affecting initiation, including basal medium, plant growth regulators, and Phytagel concentration, have been investigated in loblolly pine (Pinus taeda L.). BM₁ basal medium proved superior to DCR₁ and LP (LP basal salts plus BM₁ organic nutrients). No extrusion from megagametophytes was exhibited on LP medium. The combination of 3 mg/l 2,4-dichlorophenoxyacetic acid (2,4-D) and 0.5 mg/l 6-benzylaminopurine (BA) resulted in a higher extrusion frequency than that of 11 mg/l 2,4-D, 4.5 mg/l BA and 4.3 mg/l kinetin. Phytagel at 1 g/l resulted in the highest explant browning, but the lowest extrusion frequency, while 4 g/l Phytagel induced some dry embryogenic extrusions. Phytagel at 2 g/l was regarded as the best level for initiation of embryogenic cultures. Received: 23 December 1996 / Revision received: 22 July 1997 / Accepted: 2 September 1997     

The influence of hexavalent chromium salt on the population growth,cell morphology,and physiological parameters of the benthic microalga <Emphasis Type="Italic">Attheya ussurensis</Emphasis> Stonik,Orlova, Crawford, 2006 (BACILLARIOPHYTA) in culture

The presence of hexavalent chromium salt in culture medium negatively affected the growth dynamics and physiological parameters of the benthic microalga Attheya ussurensis. After 1 day of exposure to toxicant at concentrations of 2, 4, 7, and 10 mg/l, the cell counts were 10, 7.9, 5.6, and 4.3 × 10³ cells/ml, respectively (versus 13 × 10³ cells/ml in the control). A tendency towards a decrease in cell number remained until the end of the experiments; after 7 days of exposure the cell counts were 133, 102, 11, and 7.5 × 10³ cells/ml (versus 204 × 10³ cells/ml in the control). With increase in potassium bichromate concentration in the culture medium, there was an increase in the ratio of cell height to width and a change in the form of the cell to horseshoe shaped. The contents of chlorophyll a in microalgal cells after 1 day of exposure to 2, 4, 7, and 10 mg/l were 40, 37, 34, and 30 μg/l, respectively (45 μg/l in the control). After 7 days, at chromium salt concentrations of 2 and 4 mg/l, the chlorophyll a content was higher (670 and 647 μg/l) than in the control (605 μg/l); at 7 and 10 mg/l, it significantly decreased to 87 and 65 μg/l, respectively. The contents of carotinoids in microalgal cells after 7 days of exposure to 2 and 4 mg/l were comparable to the control values, while at 7 and 10 mg/l they decreased sharply. The amount of phaeophytin (as a percentage of total chlorophyll a content) increased with increasing potassium bichromate concentration.     

溶菌酶对瘤胃体外发酵、甲烷生成及微生物菌群结构的影响

【目的】通过体外静态模拟瘤胃发酵法研究溶菌酶对瘤胃发酵、甲烷生成及微生物菌群结构的影响。【方法】采用单因素多水平试验设计,溶菌酶添加水平分别为0(L-0,对照组)、0.1 mg/100 m L(L-0.1)、1 mg/100 m L(L-1)、10 mg/100 m L(L-10)和100 mg/100 m L(L-100),定时测定产气量和甲烷产量,培养24 h后,发酵液用于发酵参数和微生物菌群数量的q PCR测定,其中L-0、L-1和L-100三个组发酵液同时进行16S r RNA基因Illumina高通量测序。【结果】与对照组相比,低剂量溶菌酶添加(L-0.1组)不影响甲烷产量、氨氮浓度、干物质消失率、有机物消失率和总挥发性脂肪酸等瘤胃发酵参数(P0.05);随着剂量提高,L-1处理组甲烷产量、氨氮浓度显著降低(P0.05),丙酸浓度显著增加(P0.05),并且干物质消失率、有机物消失率和总挥发性脂肪酸不受影响(P0.05);而较高剂量组(L-10和L-100组)虽然甲烷产量显著降低,丙酸浓度显著增加(P0.05),但干物质消失率和有机物消失率也显著降低(P0.05)。q PCR结果显示高剂量组(L-100组)总菌、原虫、甲烷菌数量与对照组相比显著降低(P0.05),而L-0.1、L-1和L-10组总菌、真菌和原虫数量与对照组相比均无显著变化(P0.05)。高通量测序主成分分析(PCA)显示对照组与溶菌酶添加组间瘤胃细菌组成的明显区分,说明添加溶菌酶显著改变了瘤胃细菌菌群结构。溶菌酶通过增加月形单胞菌和琥珀酸弧菌等丙酸生成菌的相对丰度,使更多的氢被用于生成丙酸,导致甲烷产量降低;溶菌酶可抑制普雷沃氏菌和拟杆菌属等蛋白降解菌的生长,进而减少蛋白质过度降解,降低氨氮浓度。【结论】添加适宜浓度(1 mg/100 m L)的溶菌酶可通过调控瘤胃微生态改变瘤胃发酵模式,降低瘤胃甲烷和氨的生成,短期内并不影响饲料消化。     

Functional diversity of an aboriginal microbial community oxidizing the ore with high antimony content at 46–47°C

A procedure for rapid (7–10 days) obtaining of enrichment cultures of aboriginal thermoacidophilic microbial communities from ores with high antimony content (Sb 26%) was developed. This technique allows for rapid alkalization of the medium due to the abundance of calcites, as well as the low antioxidant status of the initial cells. The ore concentration in the medium was gradually increased to 10 g/l. In the course of this process, selection of enrichment cultures containing microbial strains preferentially oxidizing ore, S₀, or Fe²⁺ is carried out. A combination of three enrichment cultures allowed us to rapidly (in six days) adapt the aboriginal strains to high-density pulp (16%) in the reactor at 46°C, as well as to carry out a three-stage semi-continuous cultivation in the reactors at D = 0.0042 h⁻¹ and to isolate from each reactor the pure cultures of predominant bacteria involved in the process of bioleaching/oxidation of the mixture of antimonite-containing ores and sulfide flotation concentrates. It was demonstrated that, in the microbial community of reactor I, strain Sb-K exhibiting high rates of growth and initial substrate oxidation was predominant. In reactor II, strain Sb-F prevailed, showing a high substrate specificity with respect to Fe²⁺. A sulfur-oxidizing strain involved in active oxidation of reduced inorganic sulfur compounds (RISCs) was predominant in reactor III. Nevertheless, together, all three strains showed synergism and were able to oxidize S⁰, Fe²⁺, and sulfide minerals (including antimonite Sb₂S₃ in the presence of 0.02% yeast extract) in reactors. The strains differed from each other in their DNA restriction profiles, growth rates, and the rates of inorganic substrate oxidation under mixotrophic conditions. The phenotypic properties of all the studied isolates have a certain similarity to those of sulfobacilli.     

Effect of temperature and salinity on the oxygen consumption of laboratory produced Penaeus californiensis postlarvae

• 1.1. The oxygen consumption by P. californiensis postlarvae (mean wt = 0.38 g) was determined at five different temperatures and four salinities.
• 2.2. The O₂ in each chamber was recorded at 10 min intervals for 1 hr. The time course of oxygen depletion was independent of O₂ concentration down to 1.6 mg/l.
• 3.3. Oxygen consumption increased with temperature from 0.0045 mg/g/min at 19°C, to 0.0142 mg/g/min at 35°C. The thermal coefficient (Q₁₀) indicated a very high sensitivity of the postlarvae to temperature variations at 19–23°C.
• 4.4. The results show that oxygen consumption significantly depends on temperature (P < 0.001) while salinity has only a marginal effect.

     

土壤细菌呼吸对西双版纳热带森林恢复的响应

揭示不同恢复阶段热带森林土壤细菌呼吸季节变化及其主控因素,对于探明土壤细菌呼吸对热带森林恢复的响应机制具有重要的科学意义。以西双版纳不同恢复阶段热带森林(白背桐群落、崖豆藤群落和高檐蒲桃群落)为研究对象,运用真菌呼吸抑制法及高通量宏基因组测序技术分别测定土壤细菌呼吸速率和细菌多样性,并采用回归分析及结构方程模型揭示热带森林恢复过程中土壤细菌多样性、pH、土壤碳氮组分变化对土壤细菌呼吸速率的影响特征。结果表明：1)不同恢复阶段热带森林土壤细菌呼吸速率表现为：高檐蒲桃群落((1.51±0.62)CO₂ mg g^-1 h^-1)显著高于崖豆藤群落((1.16±0.56)CO₂ mg g^-1 h^-1)和白背桐群落((0.82±0.60)CO₂ mg g^-1 h^-1)(P<0.05)。2)不同恢复阶段土壤细菌呼吸速率呈显著的单峰型季节变化(P<0.05),最大值均出现在9月：高檐蒲桃群落((...     

Effect of different salt adaptation strategies on the microbial diversity, activity, and settling of nitrifying sludge in sequencing batch reactors

The effect of salinity on the activity of nitrifying bacteria, floc characteristics, and microbial community structure accessed by fluorescent in situ hybridization and polymerase chain reaction–denaturing gradient gel electrophoresis techniques was investigated. Two sequencing batch reactors (SRB₁ and SBR₂) treating synthetic wastewater were subjected to increasing salt concentrations. In SBR₁, four salt concentrations (5, 10, 15, and 20 g NaCl/L) were tested, while in SBR₂, only two salt concentrations (10 and 20 g NaCl/L) were applied in a more shock-wise manner. The two different salt adaptation strategies caused different changes in microbial community structure, but did not change the nitrification performance, suggesting that regardless of the different nitrifying bacterial community present in the reactor, the nitrification process can be maintained stable within the salt range tested. Specific ammonium oxidation rates were more affected when salt increase was performed more rapidly and dropped 50% and 60% at 20 g NaCl/L for SBR₁ and SBR₂, respectively. A gradual increase in NaCl concentration had a positive effect on the settling properties (i.e., reduction of sludge volume index), although it caused a higher amount of suspended solids in the effluent. Higher organisms (e.g., protozoa, nematodes, and rotifers) as well as filamentous bacteria could not withstand the high salt concentrations.     

Mass culture of the protozoa Colpoda steinii

Growth of the ciliate, Colpoda steinii, was studied in shake flasks, 30-l., stirred jars, and a conventional 50-gal. stainless-steel fermentor. This organism was growth with either washed or unwashed Escherichia coli cells as the sole food source. Generation times of 3–4 hr. were obtained at 30°C. With average yields of 78% (0.78 g. of protozoa/g. of bacteria). In a 100-l. fermentation, a dry weight concentration of 12.5 g./l. (1.04 × 10⁷ protozoa/ml.) was reached by means of periodic addition of E. coli paste. The influence of bacterial concentration on the growth rate of the protozoa was also investigated. It was found that this relationship could be represented by a Michaelis-Menten equation with a maximum specific growth rate of 0.23 hr. ^?1 (3-hr. generation time) and a bacterial concentration for half-maximum growth rate of 6.0 mg. (dry wt.)/l.     

The use of biomarkers in Daphnia magna toxicity testing. IV. Cellular Energy Allocation: a new methodology to assess the energy budget of toxicant-stressed Daphnia populations

The Cellular Energy Allocation (CEA) methodology wasdeveloped as biomarker technique to assess the effectof toxic stress on the energy budget of testorganisms. This short-term assay is based on thebiochemical assessment of changes in the energyreserves (total carbohydrate, protein and lipidcontent) and the energy consumption (electrontransport activity). The CEA methodology was evaluatedusing Daphnia magna juveniles exposed for 96hto sublethal lindane and mercury chlorideconcentrations. The ecological relevance of the CEAassay was assessed by comparing the sub-organismalresponse with population level parameters (obtainedfrom 21 day life table experiments) such as theintrinsic rate of natural increase (r_m) and themean total offspring per female. Two differentmethodologies were used to assess the effect levels:the no (lowest) observed effect level (NOAECs-LOAECs)approach and the regression-based approach. Bothtoxicants caused a significant decrease in the netenergy budget of D. magna, with a LowestObserved (Adverse) Effect Concentration (LOAEC) of0.18 mg/l and 5.6 µg/l for lindane andHgCl₂,respectively. Changes in the lipid content of theorganisms were detected at toxicant concentrationslower than those affecting the total carbohydrate andprotein content. Toxicant specific effects wereobserved on the electron transport activity.Comparison of the CEA results with those of thepopulation level tests revealed that for mercury theCEA based LOAEC was a three times lower than thatbased on r_m and the total brood size(18 µg/l). For lindane the CEA based LOAEC was twotimes lower than the LOAEC based on r_m(0.32 mg/l) but was higher than that based on thetotal number of offspring produced (0.1 mg/l).Using the regression-based approach, EC₁₀ valueswere calculated using three parameter sigmoid orlogistic models. Comparison between the CEA andr_m based EC₁₀ values demonstrates that forboth chemicals similar effect concentrations areobtained: the CEA-based EC₁₀ (0.20 mg/l) forlindane is 1.5 times higher than the r_m-basedEC₁₀ threshold (0.13 mg/l), while for mercury thebiomarker-based EC₁₀ value (9 µg/l) was 1.4times lower than the population-based EC₁₀ value(12.5 µg/l).From these results, we suggest that the short-term CEAassay may be useful for predicting long-term effectsat the population level. The consequences of theobserved effects on the energy budget of the testorganism are discussed in the context of the effectsemerging at the population and community level.     

Methanogenic degradation of hydroquinone in an anaerobic fixed-bed reactor

Summary A 500-ml fixed-bed reactor filled with glass sinter spools was used to study the dynamics and potential of methanogenic hydroquinone degradation. The concentration of hydroquinone as sole energy and carbon source in the inflowing medium varied from 0.55 to 2.2 g/l. Degradation of hydroquinone to methane and CO₂ was complete at low flow rates (170 ml/h) and low hydroquinone concentrations (0.55 g/l). At higher hydroquinone concentrations and/or higher flow rates, acetate accumulated in the reactor, and traces of hydroquinone were detected in the outflowing medium. The maximum degradation rate was 0.3–0.4 hydroquinone/h per 500 ml reactor volume. The bacterial community that established in the reactor after several weeks of operation was fairly stable, and consisted primarily of three bacterial species: a rod-shaped bacterium responsible for the degradation of hydroquinone to acetate and hydrogen, and two species of methanogenic bacteria, Methanospirillum hungatei and Methanothix sp.     

Acute toxicity of a household bleach,sodium hypochlorite,to a whirligig beetle Orectogyrus alluaudi Régimbart, 1889 (Coleoptera: Gyrinidae)

Acute response of Orectogyrus alluaudi Régimbart, 1889 to sodium hypochlorite was reported after a 48-h acute toxicity test in an imitated field condition. O. alluaudi belongs to the water beetle family Gyrinidae (whirligig beetles) which includes more than 700 species. The test organisms were exposed to various concentrations of sodium hypochlorite ranging from 10 to 160 mg/l along with the control, and median lethal concentration (LC₅₀) values at 24 and 48 h of exposure were assessed. Mortality increased with the concentration of exposure. The 24 and 48 h LC₅₀ values estimated for sodium hypochlorite were 87.30 (73.21–107.06) and 72.32 (62.24–84.53) mg/l, respectively. A significant mortality (P < 0.001) was observed at 40, 80 and 160 mg/l of sodium hypochlorite when compared with the control. Addition of sodium hypochlorite altered the alkalinity and pH of the test water. Behavioural responses such as agitation and disorientation were also observed. The finding showed that indiscriminate use of the household bleach would have serious impact on the bionomics of this species.     

Seasonal Changes in the Structure of the Anoxygenic Phototrophic Bacterial Community in Lake Mogilnoe,a Relict Lake on Kil'din Island in the Barents Sea

An anaerobic phototrophic bacterial community in Lake Mogilnoe, a relict lake on Kil'din Island in the Barents Sea, was studied in June 1999 and September 2001. Irrespective of the season, the upper layer of the anaerobic zone of this lake had a specific species composition of sulfur phototrophic bacteria, which were dominated by the brown-colored green sulfur bacterium Chlorobium phaeovibrioides. The maximum number of sulfur phototrophic bacteria was observed in June 1999 at a depth of 9 m, which corresponded to a concentration of bacteriochlorophyll (Bchl) e equal to 4.6 mg/l. In September 2001, the maximum concentration of this pigment (3.4 mg/l) was found at a depth of 10 m. In both seasons, the concentration of Bchl a did not exceed 3 μg/l. Purple sulfur bacteria were low in number, which can be explained by their poor adaptation to the hydrochemical and optical conditions of the Lake Mogilnoe water. In June 1999, the water contained a considerable number of Pelodictyon phaeum microcolonies and Prosthecochloris phaeoasteroides cell chains, which was not the case in September 2001. A 16S rDNA-based phylogenetic analysis of pure cultures of phototrophic bacteria isolated from the lake water confirmed that the bacterial community is dominated by Chl. phaeovibrioides and showed the presence of three minor species, Thiocystis gelatinosa, Thiocapsa sp., and Thiorhodococcus sp., the last of which is specific to Lake Mogilnoe.     

A mathematical model of kinetics of the biosynthesis of tetracyclines

Summary A mathematical model simulating the behaviour or Streptomyces aureofaciens in batch culture under conditions when tetracyclines are synthesized in excessive amounts has been formulated. The response of the mathematical model to the experimental conditions applied corresponds with data obtained in the experiments. The mathematical model demonstrated that the level of tetracycline production is determined during the period of culture growth beginning with exhaustion of inorganic phosphate from the medium and ending with inhibition of the synthesis of enzymes caused by the synthesized tetracyclines. Further tetracycline synthesis is then proportional to the amount of enzymes synthesized in this interval.List of symbols E Activity of ACT-oxygenase (10×nkat/g) - P Product concentration (mg/l) - k ₁-k ₆ Rate constants - K _S Saturation constant (g sugar/l) - K _I1 Inhibition constant (mg product/l) - K _I2 Inhibition constant (mM phosphate/l) - K _I3 Inhibition constant (mg product/l) - S ₁ Substrate sucrose (g sugar/l) - S ₂ Substrate concentration — phosphate (mM/l) - r _P Specific rate of product formation (mg product/g · h) - r _E Specific rate of enzyme synthesis (10×nkat/g² · h), Expressed by activity units - t Cultivation time (hour) - X Biomass dry weight (g/l) - Y _S/X Yield coefficient - Specific growth rate (h^-1)     

The effects of copper,cadmium and zinc on particle filtration and uptake of glycine in the pacific oyster Crassostrea gigas

1. The filtration rate (volume of water completely cleared of collodial carbon per unit time) by control oysters is 36.60 ml/g hr ± 7.68 (sd).2. Filtration rates decrease with increasing concentrations of Cd²⁺ and Zn²⁺.3. In 8–16 mg/l Cu²⁺, filtration rates are significantly higher than the control, but in Cu²⁺ concentrations above 32 mg/l, filtration rates are lower than controls.4. Influx of ¹⁴C-glycine is characterized by Michaelis-Menten kinetics with J_max and K_t values of 1.85 ± 0.097 μmol/g hr and 33.7 ± 4.6 μM respectively.5. The uptake rate of glycine from 1 μM solution is 37.79 μmol/g hr.6. In order of degree of inhibition of glycine uptake, Cu²⁺ > Cd²⁺ > Zn²⁺.7. In 128 mg/l Cu²⁺, glycine uptake rate is reduced to 3.96 nmol/g hr or 10.5% of control.8. The rate of glycine uptake by filter feeding bivalves is dependent on rate of water pumping rate.9. The volume specific glycine transport (amount of glycine transported/unit volume of seawater completely cleared of colloidal carbon) by control oysters in 1 μM glycine concentrations is 1.03 μmol/l.10. The volume specific glycine transport remains constant in increasing Zn²⁺ concentrations, and declines in increasing Cu²⁺ concentrations, suggesting differential effects of the metals on particle filtration and the epithelial amino acid carriers.11. The apparent volume specific glycine transport increases to 2.14 μmol/l in 128 mg/l Cd²⁺. This volume specific transport greater than the glycine concentration in the medium suggests that there may be uptake of cadmium complexed glycine by the oysters.     

Carbon partitioning into sorbitol,sucrose, and starch in source and sink apple leaves as affected by elevated CO2

Experiments were conducted in controlled growth chambers to evaluate how increases in CO₂ concentration ([CO₂]) affected carbon metabolism and partitioning into sorbitol, sucrose, and starch in various ages of apple leaves. Apple plants (Malus domestica), 1 year old, were exposed to [CO₂] of 200, 360, 700, 1000, and 1600 μl l⁻¹ up to 8 days. Six groups of leaves (counted from the shoot apex): leaves 1–5 (sink), 6–7 (sink to source transition), 8–9 (sink to source transition), 10–11 (nearly-matured source), 21–22 (mid-age source), and 30–32 (aged source), were sampled at 1, 2, 4, and 8 days after [CO₂] treatments for carbohydrate analysis. Increases in [CO₂] from a sub-ambient (200 μl l⁻¹) to an ambient level (360 μl l⁻¹) significantly increased the concentrations of sorbitol, sucrose, glucose, and fructose tested in all ages of leaves. Continuous increase in [CO₂] from ambient to super-ambient levels up to 1600 μl l⁻¹ also increased sorbitol concentration by ≈50% in source leaves, but not in sink and sink to source transition leaves. Increases in [CO₂] from 360 to 1600 μl l⁻¹, however, had little effect on sucrose content in all ages of leaves. Starch concentrations increased in all ages of leaves as [CO₂] increased. Rapid starch increases (e.g. 5-, 6-, 20-, and 50-fold increases for leaf groups 1–5, 6–7, 10–11, and 21–22, respectively) occurred from 700 to 1600 μl l⁻¹ [CO₂] during which increases in sorbitol concentration either ceased or slowed down. Our results indicate that changes in carbohydrates were much more responsive to CO₂ enrichment in source leaves than in sink and sink to source transition leaves. Carbon partitioning was favored into starch and sorbitol over sucrose in all ages of leaves when [CO₂] was increased from 200 to 700 μl l⁻¹, and was favored into starch over sorbitol from 700 to 1600 μl l⁻¹ [CO₂].     

Effects of lactoferrin supplementation on ileal and total tract nutrient digestibility,gastrointestinal microbial populations,and immune characteristics of ileal cannulated,healthy, adult dogs

Abstract

Orally supplemented lactoferrin derived from bovine milk is purported to have beneficial effects on gut health of animals. Bovine lactoferrin (0, 60, or 120 mg/d) was fed to ileal cannulated, adult dogs in a replicated 3 × 3 Latin square design with 14 d periods. Control dogs tended (p = 0.06) to have higher fecal DM concentrations compared with dogs supplemented with 120 mg/d lactoferrin (34.5 vs. 32.9%). Fecal scores ranged from 3.0 – 3.3, suggesting that feces of all dogs was near the desired consistency, with dogs supplemented with 120 mg/d lactoferrin tending (p = 0.08) to have higher fecal scores. Ileal azoreductase activity tended (p < 0.10) to be higher in dogs supplemented with 60 or 120 mg/d lactoferrin (609 vs. 592 nmol/h per g ileal DM, respectively) as compared with unsupplemented dogs (272 nmol/h per g ileal DM). The following bacterial groups were measured: bifidobacteria, Campylobacter spp., Clostridium spp., eubacteria, Escherichia coli, Lactobacillus spp., Staphylococcus spp., and Streptococcus spp. Fecal streptococci concentrations were lower (p < 0.05) for dogs receiving 60 mg/d lactoferrin (8.60 log₁₀ cfu/g fecal DM) as compared with unsupplemented dogs (9.19 log₁₀ cfu/g fecal DM) or dogs receiving 120 mg lactoferrin/d (9.43 log₁₀ cfu/g fecal DM). Dogs supplemented with 120 mg/d lactoferrin tended (p = 0.08) to have higher fecal indole concentrations as compared to unsupplemented dogs (1.80 vs. 1.46 μmol/g fecal DM). Because most bacterial groups measured were unaffected, it appears that lactoferrin did not exhibit prebiotic activity, and based on the data collected, lactoferrin also did not appear to have major effects on indices of health in the dog.