Growth characteristics and expression of iron-regulated outer-membrane proteins of chemostat-grown biofilm cells of Pseudomonas aeruginosa.

An in vitro chemostat system was used to study the growth and the expression of iron-regulated outer-membrane proteins (IROMPs) by biofilm cells of Pseudomonas aeruginosa cultivated under conditions of iron limitation. The population of the planktonic cells decreased when the dilution rate was increased. At a dilution rate of 0.05 h-1, the populations of planktonic cells of both mucoid and nonmucoid P. aeruginosa were 3 x 10(9) cells/mL. This value dropped to 5 x 10(6) cells/mL when the dilution rate was increased to 1.0 h-1. The reverse was observed for the biofilm cells. The number of biofilm cells colonising the silicone tubing increased when the dilution rate was increased. The number of biofilm cells of the mucoid strain at steady state was 2 x 10(8) cells/cm (length) when the dilution rate was fixed at 0.05 h-1. The figure increased to 8 x 10(9) cells/cm when the dilution rate was increased to 1.0 h-1. The population of biofilm cells of the nonmucoid strain was 9 x 10(7) cells/cm (length) when the dilution rate was 0.05 h-1. It increased to 2 x 10(9) cells/cm when the dilution rate was set at 1.0 h-1. The expression of IROMPs was induced in the biofilm cells of both mucoid and nonmucoid strains when the dilution rates were 0.05 and 0.2 h-1. IROMPs were reduced but still detectable at the dilution rate of 0.5 h-1. However, the expression of IROMPs was repressed when the dilution rate was increased to 1.0 h-1. The data suggest that the biofilm cells of P. aeruginosa switch on the expression of IROMPs to assist iron acquisition when the dilution rate used for the chemostat run is below 0.5 h-1. The high affinity iron uptake system is not required by the biofilm cells when the dilution rate is increased because the trace amount of iron present in the chemostat is sufficient for the growth of adherent biofilm cells.     

Carbon determination in human teeth by activation with He-3 ions

A nuclear analytical method, involving activation with³He ions, was developed to determine carbon content in human teeth with well-documented histories. The tooth samples were irradiated with 2.7-MeV³He particles at 50 nA intensity, and the activity of¹⁴O induced through the reaction¹²C(³He, n)¹⁴O, determined by counting the 2.31-MeV gammas. Different dental hard tissues were studied separately. A solid piece of silver steel, the carbon content of which was accurately determined by chemical means, was used as the standard. The carbon content in different teeth varied from 4–7%. The overall experimental accuracy was better than 4.5%.

     

中国鸡皮衣属和泡鳞衣属地衣2个新记录种

报道了采自中国西北部新疆博格达山区哈熊沟森林公园的鸡皮衣属和泡鳞衣属地衣的2个中国新记录种,即南方鸡皮衣(Pertusaria australis Vian)和北极泡鳞衣(Toninia arctica Timdal),并描述了二者的形态学、解剖学以及化学成分特征,提供了其形态特征和内部解剖结构照片.标本保存于新疆大学...     

Dietary fat intake and risk of stroke in male US healthcare professionals: 14 year prospective cohort study

Objective To examine the association between intake of total fat, specific types of fat, and cholesterol and risk of stroke in men.Design and setting Health professional follow up study with 14 year follow up.Participants 43 732 men aged 40-75 years who were free from cardiovascular diseases and diabetes in 1986.Main outcome measure Relative risk of ischaemic and haemorrhagic stroke according to intake of total fat, cholesterol, and specific types of fat.Results During the 14 year follow up 725 cases of stroke occurred, including 455 ischaemic strokes, 125 haemorrhagic stokes, and 145 strokes of unknown type. After adjustment for age, smoking, and other potential confounders, no evidence was found that the amount or type of dietary fat affects the risk of developing ischaemic or haemorrhagic stroke. Comparing the highest fifth of intake with the lowest fifth, the multivariate relative risk of ischaemic stroke was 0.91 (95% confidence interval 0.65 to 1.28; P for trend = 0.77) for total fat, 1.20 (0.84 to 1.70; P = 0.47) for animal fat, 1.07 (0.77 to 1.47; P = 0.66) for vegetable fat, 1.16 (0.81 to 1.65; P = 0.59) for saturated fat, 0.91 (0.65 to 1.28; P = 0.83) for monounsaturated fat, 0.88 (0.64 to 1.21; P = 0.25) for polyunsaturated fat, 0.87 (0.62 to 1.22; P = 0.42) for trans unsaturated fat, and 1.02 (0.75 to 1.39; P = 0.99) for dietary cholesterol. Intakes of red meats, high fat dairy products, nuts, and eggs were also not appreciably related to risk of stroke.Conclusions These findings do not support associations between intake of total fat, cholesterol, or specific types of fat and risk of stroke in men.     

Microbiological Analysis of Tube-Well Water in a Rural Area of Bangladesh

Five tube-wells in Matlab, Bangladesh, were selected for analysis of selected biophysicochemical parameters. The results showed that all tube-well water samples contained zooplankton and bacteria. Results for some of the parameters were outside the accepted limits recommended by the World Health Organization for drinking water. It is concluded that water from tube-wells should be treated if used as drinking water.     

Sequencing and Expression of a β-Mannanase Gene from the Extreme Thermophile Dictyoglomus thermophilum Rt46B.1, and Characteristics of the Recombinant Enzyme

A β-mannanase gene (manA) was isolated from the extremely thermophilic bacterium Dictyoglomus thermophilum Rt46B.1. ManA is a single-domain enzyme related to one group of β-mannanases (glycosyl hydrolase family 26). The manA gene was expressed in the heat-inducible vector pJLA602 and the expression product, ManA, purified to homogeneity. The recombinant ManA is a monomeric enzyme with a molecular mass of 40 kDa and an optimal temperature and pH for activity of 80°C and 5.0. In the absence of substrate, the enzyme showed no loss of activity at 80°C over 16 h, while at 90°C the enzyme had a half-life of 5.4 min. Hydrolysis of the galactomannan locust bean gum (LBG) by purified ManA released mainly mannose, mannobiose, and mannotriose, confirming that ManA is an endo-acting β-mannanase. Sequence comparisons with related β-mannanases has allowed the design of consensus PCR primers for the identification and isolation of related genes. Received: 7 June 1999 / Accepted: 6 July 1999     

Nematicidal Activity of Some Phenolics on Root Knot, Growth and Yield of Capsicum frutescens cv. California Wonder

Abstract Free living nematode Caenorhabditis elegans was used as a test system for screening anthelmintic phenolics. The most effective concentrations (100, 500 and 1000 μg ml⁻¹) were used against root knot nematode Meloidogyne incognita. Effect of these phenolics was determined on growth and development of host plant Capsicum frutescens cv. California Wonder, Second stage juveniles of M. incognita were hatched from egg masses collected from roots of host plant and subjected to similar phenol concentrations for 48 h. Mortality of M. incognita was recorded on the basis of parameters used for test organism bioassay. Both healthy and inoculated plants of C. frutescens cv. California Wonder were treated withsolutions of salicylic acid (SA) and p-betahydroxy benzoic acid (BA) so that each pot received 100, 500 and 1000 mg phenol. Control plants were supplied with distilled water, Plants were uprooted 21 days after inoculation and roots were gall indexed. Some plants were left in the pots for further growth and development. Surface sterilised seedlings of host plant were raised and inoculated with second stage Juveniles of M. incognita. Thereafter observations were recorded on the vegetative and reproductive parameters of the plants. Drench application of SA and BA were found quite effective with no apparent phytotoxic effect.     

Halothane alters contractility and Ca2+ transport in ventricular myocytes from streptozotocin-induced diabetic rats

General anaesthetics have previously been shown to have profound effects on myocardial function. Moreover, many patients suffering from diabetes mellitus are anaesthetised during surgery. This study investigated compromised functioning of cardiac myocytes from streptozotocin (STZ)-induced diabetic rats and the additive effects of halothane on these dysfunctions. Ventricular myocytes were isolated from 8 to 12 weeks STZ-treated rats. Contraction and intracellular free calcium concentration ([Ca²⁺] _i ) were measured in electrically field-stimulated (1 Hz) fura-2-AM-loaded cells using a video-edge detection system and a fluorescence photometry system, respectively. L-type Ca²⁺ current was measured in whole cell, voltage-clamp mode. Halothane significantly (p < 0.01) depressed the amplitude and the time course of the Ca²⁺ transients in a similar manner in myocytes from control and STZ-treated rats. However, the effect of halothane on the amplitude of shortening and L-type Ca²⁺ current was more pronounced in myocytes from STZ-treated animals compared to age-matched controls. Myofilament sensitivity to Ca²⁺ was significantly (p < 0.01) increased in myocytes from STZ-treated rats compared to control. However, in the presence of halothane the myofilament sensitivity to Ca²⁺ was significantly (p < 0.05) reduced to a greater extent in myocytes from STZ-treated rats compared to controls. In conclusion, these results show that contractility, Ca²⁺ transport and myofilament sensitivity were all altered in myocytes from STZ-treated rats and these processes were further altered in the presence of halothane suggesting that hearts from STZ-induced diabetic rats are sensitive to halothane. (Mol Cell Biochem 261: 251–261, 2004)