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. 1980 Sep;40(3):659–671. doi: 10.1128/aem.40.3.659-671.1980

Effects of Grazing by Estuarine Gammaridean Amphipods on the Microbiota of Allochthonous Detritus

Susan J Morrison 1,, David C White 1
PMCID: PMC291634  PMID: 16345641

Abstract

Estuarine gammaridean amphipods grazing at natural population density on detrital microbiota affected the microbial community composition, biomass, and metabolic activity without affecting the physical structure of the leaves. Total microbial biomass estimated by adenosine triphosphate and lipid phosphate or observed by scanning electron microscopy was greater on grazed than on ungrazed detritus. The rates of oxygen consumption, poly-β-hydroxybutyrate synthesis, total lipid biosynthesis, and release of 14CO2 from radioactively prelabeled microbiota were higher on grazed than on ungrazed leaves, indicating stimulation of the metabolic activity of grazed detrital microbes. This was true with rates based either on the dry leaf weight or microbial biomass. Alkaline phosphatase activity was lower in the grazed system, consistent with enhanced inorganic phosphate cycling. The loss of 14C from both total lipid and poly-β-hydroxybutyrate of microorganisms prelabeled with 14C was greater from grazed than ungrazed microbes. There was a faster decrease in the 14C-glycolipid than in the 14C-neutral lipid or 14C-phospholipid fractions. Analysis of specific phospholipids showed losses of the metabolically stable [14C]glycerolphosphorylcholine derived from phosphatidylcholine and much more rapid metabolism of the bacterial lipid phosphatidylglycerol measured as [14C]glycerolphosphorylglycerol with amphipod grazing. The biochemical data supported scanning electron microscopy observations of a shift as the grazing proceeded from a bacterial/fungal community to one dominated by bacteria.

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Selected References

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  1. BARTLETT G. R. Phosphorus assay in column chromatography. J Biol Chem. 1959 Mar;234(3):466–468. [PubMed] [Google Scholar]
  2. BLIGH E. G., DYER W. J. A rapid method of total lipid extraction and purification. Can J Biochem Physiol. 1959 Aug;37(8):911–917. doi: 10.1139/o59-099. [DOI] [PubMed] [Google Scholar]
  3. Bobbie R. J., Morrison S. J., White D. C. Effects of substrate biodegradability on the mass and activity of the associated estuarine microbiota. Appl Environ Microbiol. 1978 Jan;35(1):179–184. doi: 10.1128/aem.35.1.179-184.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Dawes E. A., Senior P. J. The role and regulation of energy reserve polymers in micro-organisms. Adv Microb Physiol. 1973;10:135–266. doi: 10.1016/s0065-2911(08)60088-0. [DOI] [PubMed] [Google Scholar]
  5. Herron J. S., King J. D., White D. C. Recovery of Poly-beta-Hydroxybutyrate from Estuarine Microflora. Appl Environ Microbiol. 1978 Feb;35(2):251–257. doi: 10.1128/aem.35.2.251-257.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hulett-Cowling F. M., Campbell L. L. Purification and properties of an alkaline phosphatase of Bacillus licheniformis. Biochemistry. 1971 Apr 13;10(8):1364–1371. doi: 10.1021/bi00784a014. [DOI] [PubMed] [Google Scholar]
  7. Ikawa M. Bacterial phosphatides and natural relationships. Bacteriol Rev. 1967 Mar;31(1):54–64. doi: 10.1128/br.31.1.54-64.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Kates M. Bacterial lipids. Adv Lipid Res. 1964;2:17–90. [PubMed] [Google Scholar]
  9. King J. D., White D. C. Muramic acid as a measure of microbial biomass in estuarine and marine samples. Appl Environ Microbiol. 1977 Apr;33(4):777–783. doi: 10.1128/aem.33.4.777-783.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. King J. D., White D. C., Taylor C. W. Use of lipid composition and metabolism to examine structure and activity of estuarine detrital microflora. Appl Environ Microbiol. 1977 May;33(5):1177–1183. doi: 10.1128/aem.33.5.1177-1183.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Nickels J. S., King J. D., White D. C. Poly-beta-Hydroxybutyrate Accumulation as a Measure of Unbalanced Growth of the Estuarine Detrital Microbiota. Appl Environ Microbiol. 1979 Mar;37(3):459–465. doi: 10.1128/aem.37.3.459-465.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Short S. A., White D. C., Aleem M. I. Phospholipid metabolism in Ferrobacillus ferrooxidans. J Bacteriol. 1969 Jul;99(1):142–150. doi: 10.1128/jb.99.1.142-150.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. White D. C. Lipid composition of the electron transport membrane of Haemophilus parainfluenzae. J Bacteriol. 1968 Oct;96(4):1159–1170. doi: 10.1128/jb.96.4.1159-1170.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. White D. C., Tucker A. N. Phospholipid metabolism during bacterial growth. J Lipid Res. 1969 Mar;10(2):220–233. [PubMed] [Google Scholar]

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