Molecular mechanism of glucose-6-phosphate utilization in the dinoflagellate Karenia mikimotoi

Harmful Algae. 2017 Jul:67:74-84. doi: 10.1016/j.hal.2017.06.006. Epub 2017 Jul 8.

Abstract

Phosphorus (P) is an essential nutrient for marine phytoplankton as for other living organisms, and the preferred form, dissolved inorganic phosphate (DIP), is often quickly depleted in the sunlit layer of the ocean. Phytoplankton have developed mechanisms to utilize organic forms of P (DOP). Hydrolysis of DOP to release DIP by alkaline phosphatase is believed to be the most common mechanism of DOP utilization. Little effort has been made, however, to understand other potential molecular mechanisms of utilizing different types of DOP. This study investigated the bioavailability of glucose-6-phosphate (G6P) and its underlying molecular mechanism in the dinoflagellate Karenia mikimotoi. Suppression Subtraction Hybridization (SSH) was used to identify genes up- and down-regulated during G6P utilization compared to DIP condition. The results showed that G6P supported the growth and yield of K. mikimotoi as efficiently as DIP. Neither DIP release nor AP activity was detected in the cultures grown in G6P medium, however, suggesting direct uptake of G6P. SSH analysis and RT-qPCR results showed evidence of metabolic modifications, particularly that mitochondrial ATP synthase f1gamma subunit and thioredoxin reductase were up-regulated while diphosphatase and pyrophosphatase were down-regulated in the G6P cultures. All the results indicate that K. mikimotoi has developed a mechanism other than alkaline phosphatase to utilize G6P.

Keywords: Alkaline phosphatase; DOP utilization; Glucose-6-phosphate; Karenia mikimotoi; Suppression subtraction hybridization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaline Phosphatase / metabolism
  • DNA, Complementary / genetics
  • Dinoflagellida / drug effects
  • Dinoflagellida / genetics
  • Dinoflagellida / metabolism*
  • Gene Expression Profiling
  • Gene Expression Regulation / drug effects
  • Gene Ontology
  • Glucose-6-Phosphate / metabolism*
  • Molecular Sequence Annotation
  • Phosphorus / pharmacology
  • Sequence Analysis, DNA

Substances

  • DNA, Complementary
  • Phosphorus
  • Glucose-6-Phosphate
  • Alkaline Phosphatase