Purification and properties of an extracellular endo-1,4-β-glucanase fromLenzites trabea

An extracellular endo-1,4--glucanase (EC 3.2.1.4) has been isolated and purified from the culture solution of the basidiomyceteLenzites trabea grown on glucose and cellulose. Besides-glucosidase activity (EC 3.2.1.21) no evidence for C₁-activity (EC 3.2.1.91) in the culture solution was found.The endoglucanase has been purified in a four-step procedure including chromatography on Sepharose 6-B and DEAE-Sephadex A-50, adsorption on hydroxylapatite and gel filtration on Bio-Gel P-100. The enzyme showed maximum activity at pH 4.4 and 70°C. A molecular weight of 29000 Daltons was estimated by calibration on Bio-Gel P-100. The enzyme hydrolyses carboxymethyl cellulose (CMC) as well as xylan.List of Abbreviations CMC carboxymethyl cellulose - D.S. degree of substitution - D.P. degree of polymerisation - MW molecular weight     

Purification and properties of an extracellular β-glucosidase from Lenzites trabea

Summary When culturing the cellulolytic-active Basidiomycete and brown-rot fungus Lenzites trabea A-419 in submerged culture with glucose and cellulose as a carbon source, the fungus only excreted -glucosidase (EC 3.2.1.21) and an endo-1,4--glucanase (EC 3.2.1.4).No evidence for C₁ activity (EC 3.2.1.91) was found in the culture filtrate or in the ultra concentrate. -Glucosidase could be separated from endoglucanase by chromatography on Sepharose 6-B. Further fractionation of the -glucosidase on DEAE-Sephadex A-25 resulted in a 525-fold purification. The molecular weight of the isolated -glucosidase was determined by co-chromatography on Sephadex G-200 to be 320,000 daltons. The enzyme developed maximum activities at pH 4.5 and 75°C. The enzyme does not act on crystalline cellulose or CMC, but it hydrolyzes cellotriose,-tetraose, and-pentaose to cellobiose and glucose. -glucosidase activity was strongly inhibited by the reaction product, glucose. A K_i value of 2.7×10^–3 (M) for noncompetitive inhibition was found.     

DEVELOPMENT OF THE OVULE AND FEMALE GAMETOPHYTE IN EUSTACHYS PETRAEA AND E. GLAUCA (POACEAE)

The unilocular pistil in Eustachys contains a single ovule with lateral placentation. In E. petraea and E. glauca, the mature ovule is bitegmic, tenuinucellate, and amphitropous with the endostomic micropyle oriented toward the base of the locule. A single hypodermal archesporial cell enlarges to form the megasporocyte. The chalazal dyad member is larger than the micropylar one, and meiosis II is nonsynchronized. Two-thirds of the tetrads are linear and one-third T-shaped. The chalazal megaspore is functional. Initially ovoid, the two-nucleate female gametophyte becomes curved as it enlarges. The four-nucleate stage becomes wider at its extremities and constricted in the center. Synchronous mitotic divisions establish the eight-nucleate stage with four nuclei at each pole separated by a large central vacuole. In E. petraea, the maturation sequence begins with antipodal differentiation, followed by differentiation of the egg apparatus, migration of the polar nuclei to the center, and division of the antipodals to produce twelve cells. The sequence in E. glauca begins with migration of the polar nuclei followed by differentiation of the antipodals, egg apparatus, and antipodal replication to six cells. The polar nuclei fuse to form a secondary nucleus appressed to the egg cell in E. glauca and separated from it by a vacuole in E. petraea. T-tests for length measurements for various stages of development indicate that the functional megaspore and two-nucleate female gametophyte are significantly larger in E. glauca than in E. petraea. There is no significant difference in gametophyte length at the four-nucleate stage, and at the eight-nucleate stage, length in E. petraea surpasses that in E. glauca. This gap widens significantly at the mature stage. Nuclear volumes are significantly greater in E. glauca than in E. petraea in the functional megaspore and two-nucleate stage, but the volumes are similar at the four-nucleate stage. Consideration of the differences in structural complexity between the sporophyte and gametophyte generations leads to the conclusion that the female gametophytes of these species are more distinctive than are the sporophytes.     

Sympathetic discharge and vascular resistance after bed rest

Shoemaker, J. Kevin, Cynthia S. Hogeman, Urs A. Leuenberger,Michael D. Herr, Kristen Gray, David H. Silber, and Lawrence I. Sinoway. Sympathetic discharge and vascular resistance after bedrest. J. Appl. Physiol. 84(2):612-617, 1998.The effect of 6° head-down-tilt bedrest (HDBR) for 14 days on supine sympathetic discharge andcardiovascular hemodynamics at rest was assessed. Mean arterialpressure, heart rate (n = 25), musclesympathetic nerve activity (MSNA; n = 16) burst frequency, and forearm blood flow(n = 14) were measured, and forearmvascular resistance (FVR) was calculated. Stroke distance,our index of stroke volume, was derived from measurements of aorticmean blood velocity (Doppler) and R-R interval(n = 7). With these data, an index oftotal peripheral resistance was determined. Heart rate at rest wasgreater in the post (71 ± 2 beats/min)- compared with the pre-HDBRtest (66 ± 2 beats/min; P < 0.003), but mean arterial pressure was unchanged. Aortic strokedistance during post-HDBR (15.5 ± 1.1 cm/beat) was reduced frompre-HDBR levels (20.0 ± 1.5 cm/beat)(P < 0.03). Also, MSNA burstfrequency was reduced in the post (16.7 ± 2.8 beats/min)- comparedwith the pre (25.2 ± 2.6 beats/min)-HDBR condition(P < 0.01). Bed rest did not alterforearm blood flow, FVR, or total peripheral resistance. Thusreductions in MSNA with HDBR were not associated with a decrease inFVR.

     

Head-down-tilt bed rest alters forearm vasodilator and vasoconstrictor responses

To test thehypothesis that head-down-tilt bed rest (HDBR) for 14 days altersvascular reactivity to vasodilatory and vasoconstrictor stimuli, thereactive hyperemic forearm blood flow (RHBF, measured by venousocclusion plethysmography) and mean arterial pressure (MAP, measured byFinapres) responses after 10 min of circulatory arrest were measured ina control trial (n = 20) and whensympathetic discharge was increased by a cold pressor test (RHBF + coldpressor test; n = 10). Vascularconductance (VC) was calculated (VC = RHBF/MAP). In the control trial,peak RHBF at 5 s after circulatory arrest (34.1 ± 2.5 vs.48.9 ± 4.3 ml · 100 ml¹ · min¹)and VC (0.34 ± 0.02 vs. 0.53 ± 0.05 ml · 100 ml¹ · min¹ · mmHg¹)were reduced in the post- compared with the pre-HDBR tests(P < 0.05). Total excess RHBF over 3 min was diminished in the post- compared with the pre-HDBR trial (84.8 vs. 117 ml/100 ml, P < 0.002). Theability of the cold pressor test to lower forearm blood flow was lessin the post- than in the pre-HDBR test(P < 0.05), despite similarincreases in MAP. These data suggest that regulation of vasculardilation and the interaction between dilatory and constrictorinfluences were altered with bed rest.

     

Frequency analysis of tumor-reactive cytotoxic T lymphocytes in peripheral blood of a melanoma patient vaccinated with autologous tumor cells

A limiting-dilution assay was developed and used to determine the frequency of autologous tumor-reactive cytotoxic T lymphocytes (CTL) in peripheral blood of a melanoma patient MZ2, who has been free of detectable disease since several years. In this patient, the frequencies of tumor-reactive CTL spontaneously varied only by a factor of 1.5. After vaccinations with autologous mutagenized and lethally irradiated tumor cells a two- to tenfold increase in frequencies of tumor-reactive CTL was found within the first 2 weeks. Thereafter, CTL frequencies returned to values measured prior to vaccinations. We conclude, that the limiting-dilution assay applied in this study can detect changes in the T cell response to autologous tumor cells. The frequency of tumor-reactive CTL determined with this approach can serve as an immunological parameter for monitoring the T cell response to autologous tumor cells in individual cancer patients receiving tumor cell vaccinations.     

Waardenberg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: First report of the WS consortium

Previous studies have localized the gene for Waardenburg syndrome (WS) type I to the distal portion of chromosome 2q, near the ALPP locus. We pooled linkage data obtained from 41 WS type I and 3 WS type II families which were typed for six polymorphic loci on chromosome 2q in order to refine the location of the WS locus (WS1) and evaluate the extent of genetic heterogeneity. In the course of this work, we developed diagnostic criteria for genetic and phenotypic studies. Our findings, based on two-locus and multilocus analysis using a linkage map established from reference pedigrees, suggest that there are two or more mutations causing WS, one of which (i.e., WS1) is located on chromosome 2q, between the ALPP and FN1 loci, at distances of 7.8 cM and 11.2 cM for each marker, respectively. The results also indicate that WS1 is responsible for the illness in approximately 45% of all families in this sample. However, the odds favoring this position over a location between ALPP and SAG are only 2:1 when alternate assumptions about the proportion of linked families are considered. We conclude that a more saturated map of this region of chromosome 2q, including highly polymorphic markers, will be needed to accurately distinguish linked families and, ultimately, isolate the mutant gene.