Literature DB >> 16593912

Size of bacterial ice-nucleation sites measured in situ by radiation inactivation analysis.

A G Govindarajan1, S E Lindow.   

Abstract

Four bacterial species are known to catalyze ice formation at temperatures just below 0 degrees C. To better understand the relationship between the molecular structure of bacterial ice-nucleation site(s) and the quantitative and qualitative features of the ice-nucleation-active phenotype, we determined by gamma-radiation analysis the in situ size of ice-nucleation sites in strains of Pseudomonas syringae and Erwinia herbicola and in Escherichia coli HB101 carrying the plasmid pICE1.1 (containing a 4-kilobase DNA insert from P. syringae that confers ice-nucleation activity). Lyophilized cells of each bacterial strain were irradiated with a flux of gamma radiation from 0 to 10.2 Mrad (1 Mrad = 10(6) J/kg). Differential concentrations of active ice nuclei decreased as a first-order function of radiation dose in all strains as temperature was decreased from -2 degrees C to -14 degrees C in 1 degrees C intervals. Sizes of ice nuclei were calculated from the gamma-radiation flux at which 37% of initial ice nuclei active within each 1 degrees C temperature interval remained. The minimum mass of a functional ice nucleus, active only between -12 degrees C and -13 degrees C, was about 150 kDa for all strains. The size of ice nuclei increased logarithmically with increasing temperature from -12 degrees C to -2 degrees C, where the estimated nucleant mass was 19,000 kDa. The ice nucleant in these three bacterial species may represent an oligomeric structure, composed at least in part of an ice gene product that can self-associate to assume many possible sizes.

Entities:  

Year:  1988        PMID: 16593912      PMCID: PMC279765          DOI: 10.1073/pnas.85.5.1334

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  22 in total

1.  Radiation inactivation of enzymes inside and outside intact cells.

Authors:  W F POWELL; E POLLARD
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2.  Radiation sensitivity of enzymes in wet and in dry yeast cells.

Authors:  F HUTCHINSON; A PRESTON; B VOGEL
Journal:  Radiat Res       Date:  1957-11       Impact factor: 2.841

3.  Deuteron cross section of beta-amylase in vitro and in vivo.

Authors:  J JAGGER; D WILSON
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4.  Relationship between Ice Nucleation Frequency of Bacteria and Frost Injury.

Authors:  S E Lindow; S S Hirano; W R Barchet; D C Arny; C D Upper
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Authors:  K J Angelides; T J Nutter; L W Elmer; E S Kempner
Journal:  J Biol Chem       Date:  1985-03-25       Impact factor: 5.157

6.  Membrane enzyme systems. Molecular size determinations by radiation inactivation.

Authors:  G R Kepner; R I Macey
Journal:  Biochim Biophys Acta       Date:  1968-09-17

7.  Functional molecular weight of the lac carrier protein from Escherichia coli as studied by radiation inactivation analysis.

Authors:  T Goldkorn; G Rimon; E S Kempner; H R Kaback
Journal:  Proc Natl Acad Sci U S A       Date:  1984-02       Impact factor: 11.205

8.  The influence of low temperature on the radiation sensitivity of enzymes.

Authors:  E S Kempner; H T Haigler
Journal:  J Biol Chem       Date:  1982-11-25       Impact factor: 5.157

9.  Cloning and expression of bacterial ice nucleation genes in Escherichia coli.

Authors:  C Orser; B J Staskawicz; N J Panopoulos; D Dahlbeck; S E Lindow
Journal:  J Bacteriol       Date:  1985-10       Impact factor: 3.490

10.  Functional size of the human asialoglycoprotein receptor as determined by radiation inactivation.

Authors:  A L Schwartz; C J Steer; E S Kempner
Journal:  J Biol Chem       Date:  1984-10-10       Impact factor: 5.157

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  31 in total

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Authors:  S P Graether; Z Jia
Journal:  Biophys J       Date:  2001-03       Impact factor: 4.033

Review 2.  Physiological and ecological significance of biological ice nucleators.

Authors:  Rolv Lundheim
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2002-07-29       Impact factor: 6.237

3.  Novel method for identifying bacterial mutants with reduced epiphytic fitness.

Authors:  S E Lindow
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4.  Components of ice nucleation structures of bacteria.

Authors:  M A Turner; F Arellano; L M Kozloff
Journal:  J Bacteriol       Date:  1991-10       Impact factor: 3.490

5.  Measurement of ice nucleation-active bacteria on plants and in precipitation by quantitative PCR.

Authors:  Thomas C J Hill; Bruce F Moffett; Paul J Demott; Dimitrios G Georgakopoulos; William L Stump; Gary D Franc
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6.  Characteristics of Insertional Mutants of Pseudomonas syringae with Reduced Epiphytic Fitness.

Authors:  S E Lindow; G Andersen; G A Beattie
Journal:  Appl Environ Microbiol       Date:  1993-05       Impact factor: 4.792

7.  A biological sensor for iron available to bacteria in their habitats on plant surfaces.

Authors:  J E Loper; S E Lindow
Journal:  Appl Environ Microbiol       Date:  1994-06       Impact factor: 4.792

8.  Characterization of biological ice nuclei from a lichen.

Authors:  T L Kieft; T Ruscetti
Journal:  J Bacteriol       Date:  1990-06       Impact factor: 3.490

9.  Preordering of water is not needed for ice recognition by hyperactive antifreeze proteins.

Authors:  Arpa Hudait; Daniel R Moberg; Yuqing Qiu; Nathan Odendahl; Francesco Paesani; Valeria Molinero
Journal:  Proc Natl Acad Sci U S A       Date:  2018-07-09       Impact factor: 11.205

10.  High-level expression of ice nuclei in a Pseudomonas syringae strain is induced by nutrient limitation and low temperature.

Authors:  M Nemecek-Marshall; R LaDuca; R Fall
Journal:  J Bacteriol       Date:  1993-07       Impact factor: 3.490

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