-
Volume 14,
Issue 2,
1956
Volume 14, Issue 2, 1956
- Article
-
-
-
Some Factors Affecting Lactase Formation and Activity in Saccharomyces fragilis
More LessSUMMARY: A method for determining the lactase activity of Saccharomyces fragilis is described. The yeast is treated with cetyltrimethylammonium bromide, and the products of lactose hydrolysis are fermented with S. mandshuricus. The formation of lactase in S. fragilis was studied by using the continuous culture technique. Lactase formation was inhibited by the presence of sugars in the medium at concentrations greater than 0·001% (w/v), but the magnitude of the inhibition and the range of activity over which it occurred depended on the nature of the sugar in the medium. With media containing glucose or sucrose, activities up to 10 units lactase/mg. dry weight were found when the sugar concentration was less than 0·001% (w/v), while at high concentrations lactase activity was almost completely absent. With media containing galactose or lactose at concentrations less than 0·001% (w/v) activities of approximately 100 units lactase/mg. dry weight were observed, while at concentrations greater than 0·01% (w/v) the activity was less. The mean generation time of the organisms and the concentrations of growth factors, ammonium and hydrogen ions had, over the range tested, no significant effect on lactase formation. The lactase activity found in intact organisms was always lower than the activity found in disrupted organisms, irrespective of the conditions under which the yeast had been grown. Possible interpretations of this phenomenon are discussed.
-
-
-
-
Antibiotic Activity of Actinomycetes in Soil and their Controlling Effects on Root-rot of Wheat
More LessSUMMARY: A study has been made of conditions affecting the production of antibiotics in three soils by a number of unidentified Streptomyces spp. capable of inhibiting a variety of test organisms in vitro. In actinomycete-inoculated soils, antibiotic production was demonstrated only in sterile soils supplemented with a suitable organic source. The greatest accumulations of antibiotics were found in a neutral soil with added glucose (2·5%) while under similar conditions, no antibioties, or only traces were recovered from acid and alkaline soils. Antibiotics, however, could be recovered from inoculated acid soil, following neutralization and the addition of glucose. Fresh grass (3%), clover (3%) and soybean meal (2%) were also suitable supplements for antibiotic production by the majority of the actinomycetes, though the amounts of antibiotics were considerably less than in glucose-treated soils.
In greenhouse experiments the assessment of root damage to wheat seedlings in sterile soil demonstrated that all the actinomycetes tested significantly reduced the degree of root-rot caused by Helminthosporium sativum. In the neutral and alkaline soils a relationship was evident between disease incidence and degree of antagonism exhibited by actinomycetes in vitro, suggesting that antibiotics were responsible. No such relationship was observed between disease control and the antibiotic-producing abilities of the actinomycetes in soil as determined by standard assay procedures.
-
-
-
Effects of Clupein and of its Degradation Products on a Rhizobium Bacteriophage, on its Host Bacterium and on the Interaction between the two
More LessSUMMARY: Clupein at 0·02–0·05% in the liquid nutrient medium used to cultivate nodule bacteria, rapidly killed the bacteria and slowly inactivated a bacteriophage that attacked them. When added to a bacterial culture in liquid medium before adding phage, clupein prevented phage and bacteria from combining; when added after the two had combined, clupein interrupted further stages of phage-host interaction. Clupein at 0·0016% acted bacteriostatically and slowed phage multiplication but did not stop it.
Trypsin and chymotrypsin hydrolyse clupein, trypsin breaking about twice as many peptide bonds as chymotrypsin. At a concentration corresponding to 0·02–0·05% clupein, the peptides produced by chymotrypsin acted bacteriostatically in the liquid nutrient medium; the peptides inactivated phage much more slowly than did intact clupein, and they inhibited phage multiplication by interfering with the combination between phage and host. When added after phage and bacteria had combined, the peptides did not interfere with further stages of phage-host interaction. The smaller peptides produced by trypsin had no effect on host bacteria, phage, or phage/host interaction.
Phage preparations partially inactivated by clupein had their activity partially restored by incubation with trypsin or chymotrypsin.
Clupein, but none of its hydrolytic products, made phage with much non-phage material sedimentable by slow-speed centrifugation.
-
-
-
Observations on the Anomalous Proteins Occurring in Extracts from Plants Infected with Strains of Tobacco Mosaic Virus
More LessSUMMARY: When extracts from plants infected with various strains of tobacco mosaic virus were ultracentrifuged, the non-infective supernatant fluids still contained 0·5-5% of the protein serologically related to the viruses. The small, mostly spherical, particles aggregated to form short rods as the antigen was progressively purified by precipitation with acid or salts. It formed long rods when heated in pH 5·5 buffer or when incubated with trypsin. As the particles increased in length, their serological behaviour in precipitation tests changed from ‘somatic’ to ‘flagellar’ type.
Purified preparations of the unsedimented antigen from plants infected with either of two virus strains contained 0·1–0·2% phosphorus, seemingly in the form of a ribose nucleic acid. No evidence was obtained that the preparations were mixtures containing some particles with the 0·5% phosphorus characteristic of infective virus and some particles of protein free from nucleic acid.
One virus strain produced a higher ratio than the others of unsedimented to sedimented antigen. The amount of unsedimented antigen was correlated with the total content of anomalous protein when the protein was increasing rapidly, but later it fluctuated unpredictably. No conditions were found that consistently favoured its accumulation, but when plants systemically infected with the type strain were kept at 36 °, the total amount of antigen decreased, while the amount unsedimented sometimes increased.
The proportion of the total antigen now obtained as poorly infective nucleoprotein is much less than 10 years ago, when a third of it sedimented in the ultracentrifuge but failed to compact into a pellet. Now the uncompacted sediment, with all the host plants and virus strains used, contains only a trivial part of the total antigen. The virus released into sap when leaves are minced is, weight for weight, more infective than the virus that remains in the leaf residues until it is released by fine grinding.
-
-
-
The Kinetics of Urease Activity in Corynebacterium renale
More LessSUMMARY: The urease activity of Corynebacterium renale has been studied in washed suspensions and in cell-free extracts of the micro-organism. The urease is constitutive, and whole organisms have a urease activity of 17,000-22,000μg. NH3/mg. dry wt. organisms/hr. in 0·5m-urea in phosphate buffer at pH 7·0. In a cell-free extract the enzyme is optimally active at pH 7·5, has a Michaelis constant of 0·030m, and a temperature velocity constant of 7800 cal.; the activity is inhibited by atmospheric oxygen and by thiourea, but not by sixteen other analogues of urea tested.
-
-
-
Saccharomyces pretoriensis n.sp.—from South African Soil
More LessSUMMARY: A new Saccharomyces species has been isolated from soil. It is distinguished from other species of the genus by its ability to ferment glucose, galactose, sucrose, maltose and raffinose 1/3, as well as by its small cells and the formation of protuberances resembling conjugation tubes during sporulation.
-
Volumes and issues
-
Volume 171 (2025)
-
Volume 170 (2024)
-
Volume 169 (2023)
-
Volume 168 (2022)
-
Volume 167 (2021)
-
Volume 166 (2020)
-
Volume 165 (2019)
-
Volume 164 (2018)
-
Volume 163 (2017)
-
Volume 162 (2016)
-
Volume 161 (2015)
-
Volume 160 (2014)
-
Volume 159 (2013)
-
Volume 158 (2012)
-
Volume 157 (2011)
-
Volume 156 (2010)
-
Volume 155 (2009)
-
Volume 154 (2008)
-
Volume 153 (2007)
-
Volume 152 (2006)
-
Volume 151 (2005)
-
Volume 150 (2004)
-
Volume 149 (2003)
-
Volume 148 (2002)
-
Volume 147 (2001)
-
Volume 146 (2000)
-
Volume 145 (1999)
-
Volume 144 (1998)
-
Volume 143 (1997)
-
Volume 142 (1996)
-
Volume 141 (1995)
-
Volume 140 (1994)
-
Volume 139 (1993)
-
Volume 138 (1992)
-
Volume 137 (1991)
-
Volume 136 (1990)
-
Volume 135 (1989)
-
Volume 134 (1988)
-
Volume 133 (1987)
-
Volume 132 (1986)
-
Volume 131 (1985)
-
Volume 130 (1984)
-
Volume 129 (1983)
-
Volume 128 (1982)
-
Volume 127 (1981)
-
Volume 126 (1981)
-
Volume 125 (1981)
-
Volume 124 (1981)
-
Volume 123 (1981)
-
Volume 122 (1981)
-
Volume 121 (1980)
-
Volume 120 (1980)
-
Volume 119 (1980)
-
Volume 118 (1980)
-
Volume 117 (1980)
-
Volume 116 (1980)
-
Volume 115 (1979)
-
Volume 114 (1979)
-
Volume 113 (1979)
-
Volume 112 (1979)
-
Volume 111 (1979)
-
Volume 110 (1979)
-
Volume 109 (1978)
-
Volume 108 (1978)
-
Volume 107 (1978)
-
Volume 106 (1978)
-
Volume 105 (1978)
-
Volume 104 (1978)
-
Volume 103 (1977)
-
Volume 102 (1977)
-
Volume 101 (1977)
-
Volume 100 (1977)
-
Volume 99 (1977)
-
Volume 98 (1977)
-
Volume 97 (1976)
-
Volume 96 (1976)
-
Volume 95 (1976)
-
Volume 94 (1976)
-
Volume 93 (1976)
-
Volume 92 (1976)
-
Volume 91 (1975)
-
Volume 90 (1975)
-
Volume 89 (1975)
-
Volume 88 (1975)
-
Volume 87 (1975)
-
Volume 86 (1975)
-
Volume 85 (1974)
-
Volume 84 (1974)
-
Volume 83 (1974)
-
Volume 82 (1974)
-
Volume 81 (1974)
-
Volume 80 (1974)
-
Volume 79 (1973)
-
Volume 78 (1973)
-
Volume 77 (1973)
-
Volume 76 (1973)
-
Volume 75 (1973)
-
Volume 74 (1973)
-
Volume 73 (1972)
-
Volume 72 (1972)
-
Volume 71 (1972)
-
Volume 70 (1972)
-
Volume 69 (1971)
-
Volume 68 (1971)
-
Volume 67 (1971)
-
Volume 66 (1971)
-
Volume 65 (1971)
-
Volume 64 (1970)
-
Volume 63 (1970)
-
Volume 62 (1970)
-
Volume 61 (1970)
-
Volume 60 (1970)
-
Volume 59 (1969)
-
Volume 58 (1969)
-
Volume 57 (1969)
-
Volume 56 (1969)
-
Volume 55 (1969)
-
Volume 54 (1968)
-
Volume 53 (1968)
-
Volume 52 (1968)
-
Volume 51 (1968)
-
Volume 50 (1968)
-
Volume 49 (1967)
-
Volume 48 (1967)
-
Volume 47 (1967)
-
Volume 46 (1967)
-
Volume 45 (1966)
-
Volume 44 (1966)
-
Volume 43 (1966)
-
Volume 42 (1966)
-
Volume 41 (1965)
-
Volume 40 (1965)
-
Volume 39 (1965)
-
Volume 38 (1965)
-
Volume 37 (1964)
-
Volume 36 (1964)
-
Volume 35 (1964)
-
Volume 34 (1964)
-
Volume 33 (1963)
-
Volume 32 (1963)
-
Volume 31 (1963)
-
Volume 30 (1963)
-
Volume 29 (1962)
-
Volume 28 (1962)
-
Volume 27 (1962)
-
Volume 26 (1961)
-
Volume 25 (1961)
-
Volume 24 (1961)
-
Volume 23 (1960)
-
Volume 22 (1960)
-
Volume 21 (1959)
-
Volume 20 (1959)
-
Volume 19 (1958)
-
Volume 18 (1958)
-
Volume 17 (1957)
-
Volume 16 (1957)
-
Volume 15 (1956)
-
Volume 14 (1956)
-
Volume 13 (1955)
-
Volume 12 (1955)
-
Volume 11 (1954)
-
Volume 10 (1954)
-
Volume 9 (1953)
-
Volume 8 (1953)
-
Volume 7 (1952)
-
Volume 6 (1952)
-
Volume 5 (1951)
-
Volume 4 (1950)
-
Volume 3 (1949)
-
Volume 2 (1948)
-
Volume 1 (1947)
Most Read This Month
