Effects of some organophosphate and carbamate insecticides on nitrification and legume growth

Summary Nine insecticides (six organophosphates and three carbamates) were tested for their effects on soil nitrification, growth of legume seedlings, and growth of four species of rhizobia bacteria. No inhibition of nitrification was found at normal field rates (5 ppm) of application. Some instances of inhibition were observed at 50 ppm and at 500 ppm. Similarly, 5 ppm applications did not inhibit growth of alfalfa or sweetclover seedlings ... with one exception. Disc inhibition tests of the rhizobia bacteria showed thatRhizobium leguminosarum andRhizobium trifolii were most sensitive to the pesticides.Rhizobium meliloti, and particularlyRhizobium japonicum, were resistant to the insecticides. No consistent correlation was observed between tests on the nodulating bacteria and the tests on legume growth.Published with the approval of the Director of the North Dakota Agricultural Experiment Station as Journal Article No.309. Portion of a thesis presented by the senior author in partial fulfillment of the requirements for the M.S. degree in bacteriology at North Dakota State University.     

Effect of baygon (2-isopropoxyphenyl N-methylcarbamate) on some soil biological processes and its degradation by a Pseudomonas sp.

Summary Baygon (2-isopropoxyphenyl-N-methylcarbamate) inhibited nitrification for 4 weeks at 25 and for 16 weeks at 1250 ppm. Ammonification of peptone was stimulated by baygon. Oxidation of ammonium formed from peptone was not complete in 16 weeks at 1250 ppm. of baygon. Solubilization of tricalcium phosphate was not affected by baygon. CO₂ production from soil was depressed for 10 days. Glucose addition caused the higher depression of CO₂ production after a week. A Pseudomonas sp. degraded baygon to 2-isopropoxyphenol. re]19730507     

The effects of insecticides on the biting behaviour of wireworms (Agriotes spp.)

Filter-paper discs soaked in nutrient were used to study how insecticides affect the biting behaviour of wireworms. When wireworms were buried in soils treated with 3.7 ppm aldrin, Bayer (38156¹), N 2790 or thionazin they stopped biting several days or weeks before they died. Three out of ten wireworms slowly recovered their biting ability after being buried for 4 days in soil containing 3.7 ppm -BHC. Biting behaviour was little affected when wireworms were confined to soils containing insecticides known to be not very toxic to wireworms.Nutrient discs treated with thionazin or -BHC were bitten less often than discs containing nutrient alone. Those treated with nutrient and aldrin were bitten almost as often as nutrient discs but the wireworms later stopped biting and died.

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Die wirkungen von insektiziden auf das fressverhalten von drahtwürmern (Agriotes spp.)

Zusammenfassung Um den Einfluß von Insektiziden auf das Freßverhalten von Drahtwürmern zu prüfen, wurden auf zweierlei Weise Filtrierpapierscheiben benutzt, die mit dem Nährstoff vollgesogen waren: a) durch Zumischen der Insektizide in den Boden, so daß die Drahtwürmer ihrer Kontaktwirkung nicht entgehen konnten (Bodenbehandlung), b) durch Aufbringen der Insektizide auf die Nährscheiben selbst (Scheibenbehandlung).Drahtwürmer hörten einige Tage oder Wochen vor ihrem Tode auf zu fressen, wenn sie in Böden vergraben waren, die mit 3,7 ppm Aldrin, Bayer 38156 (O-ethyl-S-p-totyl-ethyl phosphonodithioate), N 2790 (O-ethyl-S-phenyl-ethyl-phosphonodithioate) oder Thionazin behandel waren. 3 von 10 Drahtwürmern gewannen ihre Freßfähigkeit langsam wieder, nachdem sie für 4 Tage in Boden vergraben gewesen waren, der mit 3,7 ppm -BHC behandelt war. Die Freßfähigkeit wurde wenig beeinflußt, wenn die Drahtwürmer in Boden eingeschlossen wurden, der Bromophos, Dichlofenthion, Ethion oder RD 14838 (3-isopropylphenyl N-acetyl N-methylcarbamate) enthielt, von denen keines sehr giftig für Drahtwürmer ist.Wenn die Insektizide den Nahrungsscheiben zugefügt wurden, wurden die mit Thionazin oder -BHC behandelten Scheiben weniger oft befressen als diejenigen, die nur die Nahrung enthielten. Mit Nahrungsstoffen und Aldrin behandelte Scheiben wurden bereitwillig befressen, aber die Drahtwürmer hörten später zu fressen auf und starben.

     

SO2 and NO2 effects on microbial activity in an acid forest soil

The rate of glucose decomposition and the pH fell in a forest soil (initial pH 4.06) exposed to 1.0 ppm SO₂. No such effect was noted if the soil was exposed to 1.0 ppm nitrogen dioxide (NO₂). Nitrite but not bisulfite (5g N or S/g of soil) inhibited O₂ consumption and CO₂ evolution in the glucose-amended forest soil, and nitrite and bisulfite acted synergistically in inhibiting these processes. Iron and manganese were solubilized when the soil was exposed to 10 ppm SO₂, but NO₂ caused no such change.     

Retinoylation Reaction of Proteins in Leydig (TM-3) Cells

The covalent incorporation of [³H]all-trans-retinoic acid into proteins has been studied in Leydig (TM-3) cells. The maximum retinoylation activity of Leydig cells proteins was 570± 27 fmoles/8×10⁴ cells at 37C. About 95% of [³H]retinoic acid was trichloroacetic acid-soluble after proteinase-K digestion or after hydrolysis with hydroxylamine. Thus, retinoic acid is most probably linked to proteins as a thiol ester. The retinoylation process was inhibited by 13-cis-retinoic acid and 9-cis-retinoic acid with IC₅₀ values of 0.6 and 1.2 M respectively. Dibutyryl-cAMP and forskolin increased the retinoylation activity by 75 and 81% at 500 and 25 M respectively. Also hCG increased the retinoylation binding activity of 110% at 250 ng/mL. After cycloheximide treatment of the Leydig cells the binding activity of [³H]RA was about the same that in the control, suggesting that the bond occurs on proteins in pre-existing cells. Retinoylation was not inhibited by high concentrations of palmitic or myristic acids (500 M); on the contrary, there was an increase of the binding activity of about 60 and 50% respectively.This paper is dedicated to the memory of Prof. J. A. Olson.     

Isolation and characterization of a Pseudomonas strain that degrades 4-acetamidophenol and 4-aminophenol

Though many microorganisms that are capable of using phenol as sole sourceof carbon have been isolated and characterized, only a few organisms degradingsubstituted phenols have been described to date. In this study, one strain ofmicroorganism that is capable of using phenol (3000 ppm), 4-aminophenol(4000 ppm) and 4-acetamidophenol (4000 ppm) as sole source of carbon andenergy was isolated and characterized. This strain was obtained by enrichmentculture from a site contaminated with compounds like 4-acetamidophenol,4-aminophenol and phenol in Pakistan at Bhai Pheru. The contaminated siteis able to support large bacterial community as indicated by the viable cellcounts (2 × 10⁴–5 × 10⁸) per gram of soil. Detailed taxonomic studies identified the organisms as Pseudomonas species designated as strain STI. The isolate also showed growth on other organic compounds like aniline, benzene, benzyl alcohol, benzyl bromide, toluene, -cresol, trichloroethylene and o-xylene. Optimum growth temperature and pH were found to be 30 °C and 7, respectively, while growth at 4, 25 and 35 °C and at pH 8 and 9 was also observed. Non growing suspended cells of strain ST1 degraded 68, 96 and 76.8% of 4-aminophenol (1000 ppm), phenol (500 ppm) and 4-acetamidophenol (1000 ppm), respectively, in 72 hrs. The isolation and characterization of Pseudomonas speciesstrain ST1, may contribute to efforts on phenolic bioremediation, particularly in anenvironment with very high levels of 4-acetamidophenol and 4-aminophenol.     

Cd-tolerant arbuscular mycorrhizal (AM) fungi from heavy-metal polluted soils

Spores of arbuscular mycorrhizal (AM) fungi were isolated from two heavy-metal polluted soils in France via trap culture with leek (Allium porrum L.). Preliminary identification showed that the predominant spore type of both cultures (P2 and Cd40) belongs to the Glomus mosseae group. Their sensitivity to cadmium was compared to a laboratory reference strain (G. mosseae) by in vitro germination tests with cadmium nitrate solutions at a range of concentrations (0 to 100 mg L^–1) as well as extracts from a metal-polluted and unpolluted soils. Both cultures of AM fungi from heavy-metal polluted soils were more tolerant to cadmium than the G. mosseae reference strain. The graphically estimated EC₅₀ was 0.8 mg L^–1 Cd (concentration added to the test device) for G. mosseae and 7 mg L^–1 for P2 culture, corresponding to effective Cd concentrations of approximately 50–70 g L^–1 and 200–500 g L^–1, respectively. The extract of the metal-polluted soil P2 decreased germination of spores from the reference G. mosseae but not from P2 culture. However, the extracts of two unpolluted soils with different physico-chemical characteristics did not affect G. mosseae, whereas germination of P2 spores was markedly decreased in the presence of one of the extracts. These results indicate a potential adaptation of AM fungi to elevated metal concentrations in soil. The tested spores may be considered as metal-tolerant ecotypes. Spore germination results in presence of soil extracts show the difficulty of assessing the ecotoxic effect of metals on AM fungi without considering other soil factors that may interfere in spore germination and hyphal extension.     

Acoustic intensity discrimination by the cichlid fish Astronotus ocellatus (Cuvier)

The acoustic intensity discrimination ability of the oscar (Astronotus ocellatus), a cichlid fish, was investigated using an automated positive reward method. Intensity discrimination thresholds (I, in dB) for 7-s continuous pure tone signals were measured both as functions of sound intensity above thresholds, i.e., sensation levels, (SL)(+10 dB, +20 dB and +30 dB) and frequency (200 Hz, 500 Hz, and 800 Hz). I at 500 Hz for +10 dB, +20 dB, and +30 dB SLs are 8.9, 5.5, and 3.3 dB, respectively. I (at+20 dB SL) for 200 Hz, 500 Hz, and 800 Hz are 4.5, 5.5, and 9.3 dB, respectively. Despite having poor auditory sensitivity (narrow frequency range and high thresholds), the intensity discrimination ability of the oscar follows the general trends of previously studied fish species, however, with higher thresholds.     

The effect of 2-chloro, 6-(trichloromethyl) pyridine on the chemoautotrophic metabolism of nitrifying bacteria

Studies were conducted to elucidate the mechanism of action of 2-chloro-6-(trichloromethyl)pyridine or Technical N-SERVE on the nitrification process brought about byNitrosomonas europaea. The growth ofNitrosomonas was completely inhibited in the presence of 0.2 ppm N-SERVE while 1.0 ppm of the chemical was effective in the complete inhibition of ammonia oxidation by fresh cell suspensions. Cells stored at 4 C for a period of three days required somewhat higher concentrations (1.5 ppm) of N-SERVE for the complete inhibition of their ammonia oxidizing ability while the cytochrome oxidase of these cells was inhibited to the extent of 65 to 70 percent in the presence of a corresponding amount of N-SERVE. A 45 – 70 percent reversal of the inhibition of ammonia oxidation caused by N-SERVE was obtained by the addition of 6×10^–4 M Cu⁺⁺. An equivalent concentration of Cu⁺⁺ was also effective for the complete reversal of the inhibition of cytochrome oxidase present in whole cells.Hydroxylamine oxidation by intactNitrosomonas cells was not affected by levels of N-SERVE ranging from 1 – 3 ppm. The cytochrome oxidase effective in hydroxylamine oxidation and present in cell-free extracts was not inhibited by even 100 ppm N-SERVE. Likewise, the hydroxylamine activating enzyme hydroxylamine cytochromec reductase was also not inhibited by such levels of the chemical. Raising the concentration to 170 ppm N-SERVE, however, caused a 90 percent inhibition of the enzyme.Although a 5×10^–6 M concentration of allylthiourea completely inhibited ammonia oxidation byNitrosomonas cells, concentrations up to 10^–3 M of this compound did not affect the cytochrome oxidase activity of whole cells or cell-free extracts. The inhibition of ammonia oxidation caused by 5×10^–6 M allythiourea, unlike the inhibition by N-SERVE, could not be reversed by the addition of 6×10^–4 M Cu⁺⁺.Evidence is presented that the action of N-SERVE is on that component of cytochrome oxidase which is involved in ammonia oxidation.     

The inhibition of Candida albicans by selected essential oils and their major components

Many volatile oils are known to possess antifungal properties and are potentially applicable as antimycotic agents. By studying the efficacy of essential oils against different pathogenic mycetes, we have evaluated the in-vitro inhibiting activity of some essential oils and their main constituents against a strain of Candida albicans. Sixteen commercial essential oils and forty-two pure constituents (alcohols, aldehydes, ketons, phenols and hydrocarbons), were tested by using a semisolid agar antifungal susceptibility (SAAS) method. Gas chromatography/mass spectroscopy analyses of the oils tested were performed. The essential oils of Origanum vulgare, Satureja montana, Mentha piperita, Cinnamomum verum, Cymbopogon flexuosus showed maximum inhibitory activity (MIC = 500 ppm) after 7 days. According to the results of the examination of pure constituents, -phellandrene proved to be the most interesting component among cyclic monoterpenic hydrocarbons as it showed a strong activity (MIC = 50 ppm). The most active of phenols was carvacrol (MIC 100 ppm). The open-chain alcohol 1-decanol was the most active of alcohols at 50 ppm. Finally, among aldehydes, a strong activity was shown by trans-cynnamaldehyde (MIC 50 ppm).     

A behavioral study of vibrational sensitivity in the pigeon (Columba livia)

Summary The pigeon (Columba livia) has a well-developed ability to detect weak vibrations. Using the method of heart-rate conditioning the vibrational sensitivity was determined for four pigeons at an error probability of P<0.025. The threshold-frequency relationships indicate that the greatest sensitivity to vibrational stimuli is found in the frequency range from 300 to 1,000 Hz with thresholds of about 0.1 m; lowest threshold is 0.04 m at 500 Hz (Fig. 4). Pigeons can respond not only to the frequency of a stimulus, but also to its intensity. The interval decrement (in %) of ECG is a positive correlative function of the stimulus intensity, the calculated values being approximately 4–5% per order of magnitude of the stimulus amplitude (in m) at best frequencies (Fig. 5). The value of vibration detection for birds is discussed.Abbreviation ECG electrocardiogram     

Effects of individual Bacillus thuringiensis insecticidal crystal proteins on adult Heliothis virescens (F.) and Spodoptera exigua (Hubner) (Lepidoptera: Noctuidae)

Bacillus thuringiensis (Bt) is a grampositive, spore forming bacterium, which is principally distinguishedfrom other bacilli by the production of large, insecticidal,protein crystals (Insecticidal Crystal Proteins, or ICPs). Theseproteins are usually thought to act only on the actively feedinglarvae of susceptible species by a mechanism which involvesconsumption and proteolytic processing of the protein followed bybinding to, and lysis of, midgut epithelial cells. However, few authorshave reported Bt toxicity to adult insects. In the followingpaper, we expand on previous reports of toxicity to adult insects andpresent data which demonstrate that: (1) proteolytically activated ICPssignificantly reduce the lifespans of adult Heliothis virescensand Spodoptera exigua at concentrations of 500 g/ml, butnot 167 or 25 g/ml, (2) individual activated ICPs are differentiallytoxic to adult H. virescens and S. exigua, and (3)adult S. exigua are sensitive to Cry1C protoxin at aconcentration of 1 mg/ml.Deceased     

Growth and survival of Pseudomonas cepacia DBO1(pRO101) in soil amended with 2,4-dichlorophenoxyacetic acid

The 2,4-dichlorophenoxyacetic acid (2,4-D) degrading pseudomonad, Pseudomonas cepacia DBO1(pRO101), was inoculated at approximately 10⁷ CFU/g into sterile and non-sterile soil amended with 0, 5 or 500 ppm 2,4-D and the survival of the strain was studied for a period of 44 days. In general, the strain survived best in sterile soil. When the sterile soil was amended with 2,4-D, the strain survived at a significantly higher level than in non-amended sterile soil. In non-sterile soil either non-amended or amended with 5 ppm 2,4-D the strain died out, whereas with 500 ppm 2,4-D the strain only declined one order of magnitude through the 44 days.The influence of 0,0.06, 12 and 600 ppm 2,4-D on short-term (48 h) survival of P. cepacia DBO1(pRO101) inoculated to a level of 6×10⁴, 6×10⁶ or 1×10⁸ CFU/g soil was studied in non-sterile soil. Both inoculum level and 2,4-D concentration were found to have a positive influence on numbers of P. cepacia DBO1(pRO101). At 600 ppm 2,4-D growth was significant irrespective of the inoculation level, and at 12 ppm growth was stimulated at the two lowest inocula levels. P. cepacia DBO1(pRO101) was able to survive for 15 months in sterile buffers kept at room temperature. During this starvation, cells shrunk to about one third the volume of exponentially growing cells.Abbreviations AODC acridine orange direct count - CFU colony forming units - PTYG-Agar peptone, tryptone, yeast & glucose agar - TET tetracycline - LB Luria Bertani medium     

Floristic variation within kerangas (heath) forest: re-evaluation of data from Sarawak and Brunei

The variation in species composition of trees 7.6 cm gbh in thirty-eight plots (mostly c. 0.2 ha in extent) from physiognomically-defined kerangas forest were re-analyzed by principal components analysis ordination (species centering and standardization by sample norm). Analyses were performed separately on basal area abundances, on the densities of trees in three size classes (7.6, 30.5 and 61.0 cm gbh) and on the density of small and large trees (7.6-<30.5 and 30.5-<61.0 cm gbh). A total of 636 taxa were reduced to 381 for analysis, removing those of very low density and plot frequency.Three groups of plots were identified: forest at low elevation, and generally coastal, on deep humus podzols; forest at intermediate elevation on mostly red-yellow podzols with affinities to dipterocarp forest; and forest at high elevation on mostly peaty podzols. The first group was divisible into five subgroups along a drainage gradient, while the more poorly drained plots showing affinities to peatswamp forest. Forty to eighty of the taxa, depending on the criteria for selection, were sufficient to define a stable, reduced spatial structure of the data matrix. Two subgroups, both coastal on deep podzols, represent the extreme form of kerangas forest per se. A comparison of Agathis borneensis- and Shorea albida-dominated plots revealed few other associated and differentiating taxa.Patterns were clearest from analyses of basal area data and of densities of all and small trees. Ordinations and grouping of plots for small, but not large, tree densities were similar to those for basal area. Different species were differentiated on the basis of the abundance measure, leading to group (tabular) definition of associations in a dual manner. A new system of summarization is presented which combines basal area, density and frequency in a graded hierarchical approach.The association between vegetation and soil type was difficult to unravel because of the limited environmental space sampled. Soil type was confounded with elevation, rainfall and geographical location. A major factor is clay content probably affecting nutrient status and water holding properties. Modal analysis of small tree densities showed clearest patterns in this respect. There were no patterns at the family or genus level, nor in leaf size spectra within kerangas.Problems in the treatment, analysis and summarization of tropical forest data sets are discussed. These problems centre on the scale and intensity of field sampling and the advantages of measuring small trees leading to a dual basal area and density approach. All published studies, including this one, within kerangas forest have used inadequate sampling for the purposes of revealing species changes with respect to soil type and composition.     

Influence of a carbamate pesticide on growth,respiration (14C)-carbon metabolism and symbiosis of aRhizobium sp.

Summary Addition of aldicarb (2 methyl-2(methyl thio) propionaldehyde-0-methyl carbamoyl oxime) in the growth medium enhanced the growth ofRhizobium sp. (cowpea group) at 2 ppm level while an inhibition was observed at the normal (5 ppm) and higher (10 ppm) concentrations. Respiration of the cells was also inhibited by 5 and 10 ppm levels of the chemical eventhough a stimulation was observed at 2 ppm (lower) concentration. The insecticide, when incorporated at 5 and 10 ppm levels in the medium increased the¹⁴C-glucose incorporation and considerably altered the assimilation of the radioactive carbon in different fractions of rhizobium cells. Soil application of this insecticide (Temik 10 G) reduced the number of nodules formed and the total nitrogen content in cowpea plants inoculated with theRhizobium sp. but enhanced the dry matter production of cowpea plants.Based on the M. Sc. thesis submitted by the first author to the Tamil Nadu Agricultural University, Coimbatore-3.     

Ammonium photoproduction by free and immobilized cells of Chlamydomonas reinhardtii

Summary Free-living or immobilized Chlamydomonas reinhardtii cells photoproduce ammonium from nitrite in a medium containing 1 mM of l-methionine-d,l-sulphoximine (MSX). Ammonium is accumulated in the medium to 8 mM final concentration, which inhibits nitrite uptake by the MSX-treated cells and consequently the excretion of ammonium is blocked. However, if ammonium was removed from the medium and nitrite and MSX periodically restored, the photoproduction process could be maintained over 96 h, with a final ammonium concentration of about 18 mM for free-living cells and 28 mM for immobilized ones. The MSX-treated cells showed a photoproduction productivity of 1300 mol NH ₄ ⁺ · mg chlorophyll (Chl)^-1, with an average production rate of 14 mol NH ₄ ⁺ · mg Chl^-1 per hour, for calcium alginate-entrapped cells, while the corresponding data for free-living ones was 650 mol NH ₄ ⁺ · mg Chl^-1 and 6.7 mol NH ₄ ⁺ · mg Chl^-1 per hour, respectively. Immobilized cells showed a significant increase in the nitrite uptake rate, probably due to a change in membrane permeability as a consequence of cell-matrix interactions.     

Transfection of epithelioma papulosum cyprini (EPC) carp cells

The variables involved in the transfection of epithelioma papulosum cyprini (EPC) cells (a representative carp fish cell line) with the genes for -galactosidase from E. coli, for luciferases from firefly or renilla, for the G protein of viral haemorrhagic septicemia virus or for green fluorescent protein under the cytomegalovirus, the SV40 or the T7 polymerase promoters have been studied. Fugene was selected among 10 transfection different reagents because it is simpler to use and it induced maximum efficiences of transfection of 37% equivalent to 10–15 ng -galactosidase per 500000 EPC cells.     

Regeneration of plants from callus tissue of Aeschynomene spp. (Leguminosae)

Plants were regenerated from leaflet-derived callus of Aeschynomene sensitiva, A. americana and A. villosa. Explants were induced to form callus when aseptically cultured on Murashige and Skoog medium solidified with 0.8% agar and containing 0.5 or 0.05 M naphthaleneacetic acid and 4.4 or 13.3 M benzyladenine. Shoot regeneration was readily achieved. Roots were induced when shoots were transferred to medium devoid of growth regulators or with 0.05, 0.5 or 5.4 M naphthaleneacetic acid. Plantlets were successfully transplanted to soil. Callus from A. falcata failed to regenerate shoots. Explants from leaflets of A. fluminensis did not produce callus when cultured in vitro.Abbreviations BA benzyladenine - MS Murashige and Skoog (1962) medium - NAA naphthaleneacetic acid     

In vitro propagation of cassava (Manihot esculenta Crantz)

A method is presented for the rapid in vitro propagation of cassava (Manihot esculenta Crantz). Nodal explants were induced to grow as multiple-shoot cultures on a medium containing 1.0 M 6-benzylamino purine (BAP), supplemented with 0.25 M -naphthaleneacetic acid (NAA). Nodes were removed from the shoots after three weeks of growth and subcultured on fresh culture medium. An average of 7.0 nodes were produced from each explanted node after three weeks in culture. Nodal explants were transferred to a medium containing 2.5 M indole-3-butyric acid (IBA) to improve root initiation on the developing plantlets. Plant establishment was possible upon transfer to soil. In vitro propagation offers enhanced rates of multiplication over more conventional methods of propagation. In addition, in vitro propagation facilitates the storage and international exchange of cassava germplasm.     

Separation, purification, and sequence identification of TGF-β1 and TGF-β2 from bovine milk

Cox and Bürk (Eur. J. Biochem., 1991) reported the partial characterization of Milk Growth Factor (MGF) which stimulated the migration of fibroblasts. We have fractionated the partially purified sample by RP-HPLC and obtained the separation of two peaks of activity. The two active components were isolated as pure MGF-a and MGF-b by RP-HPLC and preparative SDS-PAGE. The purified MGF-a, consisting of a single band by gel electrophoresis and a single peak on an HPLC reversed-phase C-4 column, has the same specific activity as TGF-2 in the fibroblast migration assay. MGF-a was digested by endoprotease Asp-N and the cleaved peptides were analyzed by Edman degradation and plasma desorption mass spectrometry (PDMS). The whole sequence of MGF-a determined by automated sequenator and PDMS of S-pyridylethylated protein and selected fragments was found to be identical to that of TGF-2. MGF-b protein mixture separated by SDS-PAGE was electrophoretically transferred onto a Biometra Glassybond membrane, and the blotted MGF-b protein was directly sequenced on an automated sequenator. The identified 29 amino acids sequence of MGF-b was identical to the amino-terminal sequence of TGF-1. Our study demonstrates that MGF is composed of both TGF-1 and TGF-2. TGF-2 (85%) is the predominant form.