Identification of protein X of Escherichia coli as the recA+/tif+ gene product.

Summary Protein X, molecular weight 40,000, has been separated from the other proteins of E. coliby a two-dimensional gel electrophoretic technique which separates proteins according to isoelectric point (pI) in the firstdimension and according to molecular weight in the second. When protein X is induced in wild-type cells by mitomycin C treatmentit has a pI6.0. However, when protein X is induced in a tif-1 mutant, either by temperatureshift-up to 42° or by mitomycin C treatment at 30°, it has a pI6.2. The low level of protein X which is present inuninduced tif mutants at 30° also has a pI6.2. These results suggest thattif-1 is a mis-sense mutation in the gene coding for protein X. Since transduction andcomplementation studies indicate that tif-1 is a mutation of therecA ⁺ gene (Castellazzi, Morand, George and Buttin, 1977) it follows that protein X is the recA ⁺ gene product.A model has been formulated to account for the relationship between protein X synthesis and the recA ⁺ and lexA ⁺ genes. In this model, a repressor coded by lexA ⁺ binds to the operator of the recA ⁺ gene from whence it can normally only be removed by the combined action of an inducer and protein X, the recA ⁺ product. Thus, protein X controls its own synthesis. The tif-1 mutation leads to a temperature sensitive form of protein X which, at 42°, can spontaneously remove the repressor without the intervention of the inducer.     

The genusOligolecithus Vercammen-Grandjean (Digenea: Telorchiidae) fromXenopus spp. (Anura: Pipidae), with a description ofO. siluranae n. sp. fromX. tropicalis (Gray) in Ghana

The taxonomy, host range and geographical distribution ofOligolecithus Vercammen-Grandjean, 1960, a genus of telorchiid digeneans fromXenopus spp. in Africa, is reviewed.O. jonkershoekensis Pritchard, 1964 is established as a junior synonym ofO. elianae Vercammen-Grandjean, 1960, andO. siluranae n. sp. is described fromX. tropicalis in Ghana. These two species are differentiated by variations in body length, testicular arrangement and ventral sucker width in proportion to body size.O. elianae occurs inX. laevis laevis from South Africa and Zimbabwe (new locality record),X. l. poweri from Zaire,X. l. victorianus from Zaire, Uganda and Rwanda (new locality record),X. l. bunyoniensis (new host record) from Uganda andX. l. sudanensis from Sudan (new host and locality record). It is also found inX. wittei from Uganda and Zaire andX. vestitus (new host record) from Uganda. The host ofO. siluranae belongs to a separate species group within the genusXenopus from the hosts ofO. elianae; this tropicalis group is phylogenetically isolated, but it also occurs in a different biotype, lowland tropical rain forest, ecologically distinct from the other known host species.     

Two new species of Xiphinema (Nematoda: Dorylaimida) from Colombia

Summary Two new species of Xiphinema are described from Colombia. X. colombiense n.sp. is characterized by a continuous lip region, a median vulva with both genital tracts fully developed and without Z-differentiation, a total stylet length of 197–233 m and a short, rounded tail bearing two pairs of pores and with refractive lines leading through the cuticle to a terminal depression in the protoplasm; it is differentiated from X. clavatum Heyns, 1965, X. guirani Luc & Williams, 1978, X. pyrenaicum Dalmasso, 1969, X. silvaticum Luc & Williams, 1978 and X. yapoense Luc, 1958. X. riocaquetae n.sp. is distinguished from X. macrostylum Esser, 1966. ac]19810707     

A revised polytomous key for the identification of species of the genusXiphinema Cobb, 1913 (Nematoda: Longidoridae) with exclusion of theX. americanum-group: Supplement 2

Thirty-one species and one subspecies have been described since publication of the first supplement to the polytomous key toXiphinema spp. (see Loof & Luc, 1993). Of these, 11 species belonging to the X. americanum-group are not considered here. Of the 20 remaining species, 13 are considered valid, for which identification codes are given. Three species were described earlier, but had not come to authors' notice; two of them,X. chothecolla andX. clavatus (sic) have already been synonymised withX. radicicola (see Luc & Loof, 1993); codes are given for the third species,X. codiaei. Xiphinema adenohystherum, X. cohni, X. macrogastrum, X. nuragicum andX. sphaerocephalum were considered junior synonyms ofX. pyrenaicum by Baujardet al. (1996);X. hunaniense is considered a junior synonym ofX. radicicola andX. hispanum ofX. aceri. Changes in the group and/or identification codes are made forX. aceri, X. barense, X. dentatum, X. diversicaudatum, X. filicaudatum filicaudatum, X. globosum, X. hardingi, X. paritaliae (= X. dolosum), X. paulistanum, X. pyrenaicum andX. transkeiense. The specific nameX. swarti is emended toX. swartae. Information is given for computerisation of the key.     

Evolution under the multilocus Levene model without epistasis

Evolution under the multilocus Levene model is investigated. The linkage map is arbitrary, but epistasis is absent. The geometric-mean fitness, , depends only on the vector of gene frequencies, ρ; it is nondecreasing, and the single-generation change is zero only on the set, Λ, of gametic frequencies at gene-frequency equilibrium. The internal gene-frequency equilibria are the stationary points of . If the equilibrium points of ρ(t) (where t denotes time in generations) are isolated, as is generic, then ρ(t) converges as t→∞ to some . Generically, ρ(t) converges to a local maximum of . Write the vector of gametic frequencies, p, as , where d represents the vector of linkage disequilibria. If is a local maximum of , then the equilibrium point is asymptotically stable. If either there are only two loci or there is no dominance, then d(t)→0 globally as t→∞. In the second case, has a unique maximum and is globally asymptotically stable. If underdominance and overdominance are excluded, and if at each locus, the degree of dominance is deme independent for every pair of alleles, then the following results also hold. There exists exactly one stable gene-frequency equilibrium (point or manifold), and it is globally attracting. If an internal gene-frequency equilibrium exists, it is globally asymptotically stable. On Λ, (i) the number of demes, Γ, is a generic upper bound on the number of alleles present per locus; and (ii) if every locus is diallelic, generically at most Γ−1 loci can segregate. Finally, if migration and selection are completely arbitrary except that the latter is uniform (i.e., deme independent), then every uniform selection equilibrium is a migration-selection equilibrium and generically has the same stability as under pure selection.     

Maximal power and torque-velocity relationship on a cycle ergometer during the acceleration phase of a single all-out exercise

Seven subjects pedalled on a Monark cycle ergometer as fast as possible for approximately 7 s against four different resistances which corresponded to braking torques (T _B) equal to 19, 38, 57 and 76 N · m at the crank level. Exercise periods were separated by 5-min recovery periods. Pedal velocity was recorded every 50 ms by means of a disc with 360 slots fixed on the flywheel, passing in front of a photo-electric cell linked to a microcomputer which processed the data. Every 50 ms, the time necessary to perform half a pedal revolution (t _1/2) was computed by adding the 50-ms periods necessary to reach 669 slots (the number of slots corresponding to half a pedal revolution). To measuret _1/2 to an accuracy better than 50 ms, this time was computed by a linear interpolation of the time-slot number relationship. Power (P) was averaged duringt ₁₂ by adding the power dissipated against braking torque and the power necessary to accelerate the flywheel. The torque-velocity (T-) relationship was studied during the acceleration phase of a sprint against a single TB by computing every 50 ms the relationship between and T (N · m), equal to the sum ofT _B and the torque necessary to accelerate the flywheel at the same time. The T- relationships calculated from the acceleration phase of a single all-out exercise were linear and similar to the previously described relationships between peak velocity and braking force. These relationships can be expressed as follows: = _0,acc (1 –T/T _0,acc) where is pedal velocity,T the torque exerted on the crank andT _0,acc and _0,acc have the dimensions of maximal torque and maximal velocity respectively. Based on this model, maximal power (P _max,acc) is calculated as 0.257_{0, acc} T _{0, acc}. Maximal powerP _max,acc measured with the acceleration method was independent of braking torqueT _B and slightly higher thanP _max calculated from the relationship between peak velocity andT _B.     

The pigment ofXanthomonas populi is a nonbrominated aryl-heptaene belonging to xanthomonadin pigment group 11

Based on mass spectrometry and electronic absorption spectroscopy, the main pigment fromXanthomonas populi (synonym:Aplanobacter populi) was identified as a nonbrominated aryl-heptaene. TheX. populi pigment was indistinguishable—on the basis of cochromatography and electronic absorption spectroscopy—from an authentic sample of a xanthomonadin belonging to Pigment Group 11, previously found as minor components in strains belonging to theXanthomonas campestris taxospecies (specifically in theXanthomonas pruni andXanthomonas vesicatoria nomenspecies). Possession of a xanthomonadin pigment confirms the placement ofX. populi in the genusXanthomonas and this particular pigment serves to distinguishX. populi from the five other taxospecies presently assigned to that genus. TheXanthomonas sp. isolated fromSalix, which purportedly shows affinities toX. populi, forms a monobrominated aryl-polyene pigment and —on that basis—is unlikeX. populi.     

Mechanism of sex determination inRumex hastatulus Baldw.

Summary The results presented indicate that the sex determination mechanism in the Texas race ofR. hastatulus 2n = 10 (XX + 8A); 2n = 10 (XX + 8A)] is intermediate between theX/Y andX/A systems. In this race, sex is determined to some extent by theX/A balance, but theY chromosome also affects sex expression, maleness or intersexuality being correlated with different ratios ofX andY chromosomes.The results obtained for the Texas race are fully compatible with data presented by Smith (1963) for the North Carolina race [ 2n = 8 (XX + 6A); 2n = 9 (XX ₁ Y ₂ + 6A)]. It may be concluded that evolution of the karyotype in this species is not accompanied by changes in the mechanism of sex determination.     

Synthesis of pseudopeptides containing aza-phenylalanine surrogates of the Phe-pNA motif: Influence on the binding to the human cyclophilin hCyp-18

Tripeptides bearing aza-phenylalanine derivatives Aphe-X-(4-nitrophenyl),where X is CH₂, O or NH, were synthesized starting from benzylhydrazine via a 4-step strategy. The pseudopeptides were evaluated as ligands of cyclophilin hCyp-18, an important human peptidyl-prolyl isomerase (PPIase). All pseudopeptides bind to hCyp-18, although only Suc-Ala-Pro-Phe-pNA 11 and Suc-Ala-Pro-Aphe-pNB (X = CH₂) 4 are able to inhibit the PPIase activity, suggesting that they can bind to the S1–S1 and S2–S3 subsites of hCyp-18 simultaneously. A circular dichroism study showed that only compounds 4 and 11 have -turns conformations in 0.47 M LiCl/TFE (which favors a cis-Ala-Pro conformation). In addition, the hydrazide (X = CH₂) 4 as well as the aza-urea (X = NH) 6 are resistant to both trypsin and alpha-chymotrypsin. The corresponding carbazate (X = O) 10 readily reacts with alpha-chymotrypsin and is also hydrolyzed by trypsin.     

Maximal oxygen uptake, maximal voluntary isometric contraction and physical activity in young Danish adults

In a randomly selected sample of 88 men and 115 women, aged 23–27 years from Denmark, maximal oxygen uptake ( O_2max), maximal voluntary isometric contraction (MVC) in four muscle groups and physical activity were studied. The O_2max was 48.0 ml · min^–1 kg^–1 and 39.6 ml · min^–1 · kg^–1 for the men and the women, respectively. The MVC was 10% lower than in a comparable group of Danes of the same age and height studied 35 years ago. Only in men was sports activity directly related to O_2max (ml · min^–1 · kg^–1; r=0.31, P<0.01). The MVC of the knee extensors was related to O_2max in the men (r=0.31, P<0.01), but there was no relationship between the other measurements of MVC and O_2max. In the women O_2max (ml · min^–1 · kg^–1) was only related to body size, i.e. body mass index, percentage body fat and body mass [(r= –0.47, –0.48 (both P<0.001) and –0.34. (P<0.01), respectively)]. There were differences in O_2max in the men, according to education and occupation. Blue collar workers and subjects attending vocational or trade schools in 1983 had lower O_2max and more of them were physically inactive. In the women differences were also found, but there was no clear pattern among the groups. More of the women participated regularly in sports activity, but more of the men were very active compared to the women.     

Degradation of Escherichia coli DNA: evidence for limitation in vivo by protein X, the recA gene product.

Summary DNA is more extensively degraded after it is damaged in recA mutants of E. coli than in wild type cells. All data presented here are consistent with the recA gene product, protein X, being an inhibitor of nalidixic acid induced degradation of the bulk DNA (but not of newly replicated DNA). Production of protein X also is correlated with appearance of various S.O.S. repair functions. Evidence was obtained by comparing the rates of protein X synthesis and solubilization of uniformly-labeled DNA in intact cells, incubated in the presence of nalidixic acid. A set of mutants at the lexA locus produced protein X at different rates and degraded their DNA at rates which were inversely correlated to their rates of protein X production. A low concentration of rifampicin quite specifically inhibited protein X production by wild type E. coli, and allowed more rapid DNA degradation. After the DNA was damaged by the incubation of cells in the presence of nalidixic acid, cells preloaded with protein X degraded their DNA more slowly. We propose that protein X could protect DNA against degradation by binding to singlestranded regions, thereby inhibiting nuclease action.     

Native root-nodule bacteria of traditional soybean-growing areas of northern Thailand

Over 1500 root-nodule bacteria were isolated from a range of uninoculated soybeans, and one cowpea, trap-hosts, sown in 1985 into traditional soybean-growing areas of soybean-growing areas of northern Thailand. Most isolates were slow-growing Bradyrhizobium japonicum. Using a modified bottle-jar technique, 586 of the isolates were tested with a range of soybean hosts and one cowpea host. The results indicated: