Perfusion culture of hybridoma cells recycling higher-molecular-weight components

Perfusion culture of hybridoma cells recycling higher-molecular-weight components

128 Abstracts of the Articles Printed in Hakkokogaku Kaishi A bacterium, R C O - 4 M , that c a n grow on cyclohexylacetic acid as the sole carbon s...

108KB Sizes 0 Downloads 35 Views

128

Abstracts of the Articles Printed in Hakkokogaku Kaishi

A bacterium, R C O - 4 M , that c a n grow on cyclohexylacetic acid as the sole carbon source was isolated from soil by e n r i c h m e n t cultures. T h e isolate was identified as a species of the genus Micrococcus by taxonomic studies. T h e optimal culture conditions of this organism were as follows: the growth m e d i u m consisted of cyclohexylacetic acid 0.15%, K N O a 0.25%, K H 2 P O a 0.1%, MgSO4"7H~O 0.002%, FeCla.6H~O 0.005%, CaC12.2H~O 0.002%, a n d yeast extract 0.01%, p H 8.0. T h e culture was incubated at 30°C for 3-7 d on a shaker. Strain R C O - 4 M grew on a n u m b e r of types of alicyclic compounds. A m o n g the alicyclic carboxylic acids tested, cyelohexylacetic acid a n d cyclohexylbutyric acid were the best substrates. T h e o r g a n i s m grew on cyclohexylpropionic acid, a n d grew a little on both cyclohexanecarboxylic acid a n d cyclopentanecarboxylic acid. This isolate also grew on cyclohexanone a n d cyclohexanol. Strain R C O - 4 M grew well on all of the n-alkylcyclohexanes h a v i n g 6-14 carbon atoms in the n-alkyl group, after a long lag time. * Corresponding author

[J. Ferment. Technol.,

Perfusion Culture of Hybridoma Cells Recycling Higher,Molecular-Weight Components. MICHIYUKI TOKASHIKI, ~ KIMIHIKO I-IAMAMOTO, a n d YOSHIHARU TAKAZAWA (Tokyo Research Center,

Biotechnology Research Laboratory, Teijin Limited, 4-3-2 Asahigaoka, Hino, Tokyo 191, Japan) H a k k o k o g a k u 66: 31-35. 1988. A perfusion culture was developed in which the cell-free culture s u p e r n a t a n t was ultrafiltered, a n d the retentate was recycled to the culture vessel. O n e m o u s e - m o u s e h y b r i d o m a line a n d three m o u s e - h u m a n h y b r i d o m a lines were cultured by this method. I n the culture of the m o u s e - m o u s e h y b r i d o m a 4C10B6 line using s e r u m s u p p l e m e n t e d m e d i u m , the concentration of monoclonal antibody in the culture vessel was increased in proportion to culture time, b u t cell density decreased as time passed. I n the cultures of 3 m o u s e - h u m a n h y b r i d o m a lines using serum-free m e d i u m , the concentrations of monoclonal antibodies in culture vessels increased in proportion to culture time to 20 times that of a conventional perfusion culture, a n d viable cell densities were not less t h a n those of conventional perfusion cultures. * Corresponding author

Vol. 66, 1988]

Instructions to Authors

129

Instructions to Authors for the Journal of Fermentation Technology General Policy The Journal of Fermentation Technology is devoted to the advancement and dissemination of knowledge concerning applied biology, which covers all the technological aspects of microbiology, plant and animal cell culture, enzymology, genetics, in addition to fermentation technology, biochemical engineering, food technology and the related field. Basic research which is intended for application is also welcome. Research articles submitted must be reports of unpublished original research, which are not being considered for publication elsewhere.

Types of paper Four types of papers are accepted by the Editors: These should be written in the style described on Tables I,~3 and be of the minimum length required for precise description and clear interpretation of the experiments. A concise well-written paper tends to be published more rapidly. Notes: These papers may be short research reports which contain material of unusual interest but which is not sufficient to form the basis of a full paper. Such communications must not exceed four printed pages (10 double-spaced typewritten pages) including figure(s) and table(s). Each Note must have a short abstract of no more than 50 words. Do not use section headings in the body of the Note; report methods, results and discussion in a single section. Reviews: Reviews and monographs dealing with all aspects of applied biology will be accepted. Authoritative and critical reviews of the current state of knowledge are preferred. There is no prescribed layout for reviews, but the tables, figures and manner of citations should conform to the guidelines for full papers. Letter to the editors: Letters containing brief comments or proposals of significant scientific importance will be accepted for publication. The format is optional. Full papers:

Authorship Membership in the Society of Fermentation Technology is not a prerequisite for consideration of research articles. Mailing instructions Papers offered for publication should be sent to: The Society of Fermentation Technology, Japan Business Office c/o Faculty of Engineering Osaka University 2-1 Yamada-oka, Suita-shi Osaka 565, Japan E d i t o r i a l review and revision All papers will be critically read by at least two reviewers who are selected for their competence in the subject matter of the paper. Acceptance of the paper will depend upon scientific merit and suitability for the Journal. A paper may be accepted in its original form or accepted subject to revision. The reviewers' (and editor's) suggestions will be conveyed to the author without identifying the reviewer, and the author will have an opportunity for revision. If a manuscript returned to an author for revision is held longer t h a n three months, or if revision is sufficiently extensive, the date of receipt of the revised manuscript will be substituted for the original date of