Literature DB >> 5847791

Biochemical and cellular changes occuring during conjugation in Hansenula wingei.

T D Brock.   

Abstract

Brock, Thomas D. (Indiana University, Bloomington). Biochemical and cellular changes occurring during conjugation in Hansenula wingei. J. Bacteriol. 90:1019-1025. 1954.-A technique has been devised for deagglutinating mixed populations of conjugating cells so as to be able to visualize microscopically early stages of the conjugation process. A cell can form a conjugation tube only when in contact with a cell of opposite mating type, but may do so even if the mate is unresponsive or ultraviolet-inactivated. Cell fusion occurs, however, only when both cells are able to form conjugation tubes in a region of contact. Fusion begins almost as soon as the two cells begin to form protuberances, and long before any dissolution of cell-wall material between the cells occurs. A cell which has conjugated in one region of its cell wall is still able to conjugate with another cell in another region, so that triply and quadruply conjugated cells are occasionally formed. There is no significant net increase in deoxyribonucleic acid, ribonucleic acid, protein, or carbohydrate which might be related to the conjugation process, because any minor changes that occur in these components are also detected when cells of only one mating type are incubated or when the conjugation process is inhibited with the antibiotic cycloheximide. Changes in activity of beta-1,3-glucanase (with laminarin as substrate) and beta-1,6-glucanase (with pustulan as substrate) have been measured during the conjugation process, in addition to changes in the activity of several control enzymes which would not be expected to be related to the conjugation process. Significant increases in invertase (sucrase), laminarinase, and pustulanase were detected, and minimal increases occurred in beta-glucosidase and acid phosphatase. However, these same increases were also observed in controls involving only one mating type; thus, these increases are probably not related to the conjugation process, but may be a result of other processes which probably occur during incubation in the conjugation medium.

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Year:  1965        PMID: 5847791      PMCID: PMC315770          DOI: 10.1128/jb.90.4.1019-1025.1965

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  9 in total

1.  Biochemical basis of mating in yeast.

Authors:  T D BROCK
Journal:  Science       Date:  1959-04-10       Impact factor: 47.728

2.  Physiology of the conjugation process in the yeast Hansenula wingei.

Authors:  T D BROCK
Journal:  J Gen Microbiol       Date:  1961-11

3.  Mating reaction in the yeast Hansenula wingei; preliminary observations and quantitation.

Authors:  T D BROCK
Journal:  J Bacteriol       Date:  1958-06       Impact factor: 3.490

4.  A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid.

Authors:  K BURTON
Journal:  Biochem J       Date:  1956-02       Impact factor: 3.857

5.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

6.  Studies on yeast metabolism. I. Fractionation and microdetermination of cell carbohydrates.

Authors:  W E TREVELYAN; J S HARRISON
Journal:  Biochem J       Date:  1952-01       Impact factor: 3.857

7.  Beta-glucanase of yeast.

Authors:  T D Brock
Journal:  Biochem Biophys Res Commun       Date:  1965-05-18       Impact factor: 3.575

8.  ELECTRON MICROSCOPY OF CELL FUSION IN CONJUGATING HANSENULA WINGEI.

Authors:  S F CONTI; T D BROCK
Journal:  J Bacteriol       Date:  1965-08       Impact factor: 3.490

9.  INACTIVATION OF SEXUAL AGGLUTINATION IN HANSENULA WINGEI AND SACCHAROMYCES KLUYVERI BY DISULFIDE-CLEAVING AGENTS.

Authors:  N W TAYLOR
Journal:  J Bacteriol       Date:  1964-10       Impact factor: 3.490

  9 in total
  8 in total

1.  Saccharomyces cerevisiae mutant defective in exo-1,3-beta-glucanase production.

Authors:  T Santos; F del Rey; J Conde; J R Villanueva; C Nombela
Journal:  J Bacteriol       Date:  1979-08       Impact factor: 3.490

2.  Mating reaction in Saccharomyces cerevisiae. 3. Changes in autolytic activity.

Authors:  C Shimoda; N Yanagishima
Journal:  Arch Mikrobiol       Date:  1972

3.  Conjugation in the dimorphic chromomycosis fungus Phialophora dermatitidis.

Authors:  K B Oujezdsky; P J Szaniszlo
Journal:  J Bacteriol       Date:  1973-06       Impact factor: 3.490

Review 4.  Molecular basis of mating in the yeast hansenula wingei.

Authors:  M A Crandall; T D Brock
Journal:  Bacteriol Rev       Date:  1968-09

5.  Conjugation-induced lysis of Schizosaccharomyces pombe.

Authors:  G B Calleja; B Y Yoo; B F Johnson
Journal:  J Bacteriol       Date:  1977-04       Impact factor: 3.490

6.  Synthesis of 1,3-beta-glucanases in Saccharomyces cerevisiae during the mitotic cycle, mating, and sporulation.

Authors:  F del Rey; T Santos; I García-Acha; C Nombela
Journal:  J Bacteriol       Date:  1979-09       Impact factor: 3.490

7.  Role of a cell-wall glucan-degrading enzyme in mating of Schizophyllum commune.

Authors:  J G Wessels; D J Niederpruem
Journal:  J Bacteriol       Date:  1967-11       Impact factor: 3.490

8.  Fine-structure analysis of intercellular and intracellular mitochondrial diversity in Saccharomyces cerevisiae.

Authors:  M Federman; C J Avers
Journal:  J Bacteriol       Date:  1967-10       Impact factor: 3.490

  8 in total

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