Tatiana Kulakovskaya · Evgeny Pavlov Elena N. Dedkova Editors Inorganic Polyphosphates in Eukaryotic Cells Inorganic Polyphosphates in Eukaryotic Cells Tatiana Kulakovskaya (cid:129) Evgeny Pavlov Elena N. Dedkova Editors Inorganic Polyphosphates in Eukaryotic Cells Editors Tatiana Kulakovskaya Elena N. Dedkova Laboratory of Regulation of Biochemical Department of Pharmacology Processes University of California Skryabin Institute of Biochemistry and Davis , CA Physiology of Microorganisms USA Russian Academy of Sciences Pushchino , Russia Evgeny Pavlov NYU College of Dentistry New York , New York USA ISBN 978-3-319-41071-5 ISBN 978-3-319-41073-9 (eBook) DOI 10.1007/978-3-319-41073-9 Library of Congress Control Number: 2016957150 © Springer International Publishing Switzerland 2016 T his work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is concerned, specifi cally the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfi lms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed. T he use of general descriptive names, registered names, trademarks, service marks, etc. in this publication does not imply, even in the absence of a specifi c statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use. T he publisher, the authors and the editors are safe to assume that the advice and information in this book are believed to be true and accurate at the date of publication. Neither the publisher nor the authors or the editors give a warranty, express or implied, with respect to the material contained herein or for any errors or omissions that may have been made. Printed on acid-free paper This Springer imprint is published by Springer Nature The registered company is Springer International Publishing AG Switzerland The registered company address is Gewerbestrasse 11, 6330 Cham, Switzerland Pref ace I norganic polyphosphate is a biological polymer made of many orthophosphates linked together by phosphoanhydride bonds similar to ones found in ATP. polyP is a unique macromolecule that can spontaneously form in nonliving nature and can also be enzymatically produced by living organisms. Over the past few decades, a number of exciting hypotheses regarding the role of polyP in nature have been gen- erated. These range from the concept that polyP can be a prebiotic molecule that was at the origin to living organisms to the concept that polyP can serve as a storage of biological fuel alternative to ATP. Despite its discovery over a century ago, the molecular mechanisms of polyP actions in living organisms remain poorly under- stood. In fact, most of current knowledge about biological roles of polyP comes from the studies of bacterial organisms and lower eukaryotes with very little studies of higher eukaryotes. One of the central unresolved questions in polyP research is about the relationship between its roles in different organisms. Is polyP indeed a “molecular fossil” which has a role in higher organisms that progressively dimin- ished over the evolution, or is polyP a central player in various biochemical pro- cesses throughout all kingdoms of life? Although at present it is impossible to defi nitively answer this question, recent discoveries regarding the roles of polyP support the idea that polyP maintains an important role in all living organisms including humans. This book presents a collection of chapters dedicated to the cur- rent research in the fi eld of eukaryotic polyP. It is divided in two sections with the fi rst focusing on polyP function in simple organisms and the second on polyP func- tion in higher organisms. This book is intended to bring together the perspectives of scientists working in various fi elds of life sciences, which we believe will provide a broad overview of the current state of the fi eld and help to better understand current achievements and challenges. W e would like to express the gratitude to all authors who contributed to this book for their cooperation, help, and patience. Pushchino , Russia Tatiana Kulakovskaya New York, NY , USA Evgeny Pavlov Davis , CA , USA Elena N. Dedkova v Contents Part I Lower Eukaryotes 1 The Role of Inorganic Polyphosphates in Stress Response and Regulation of Enzyme Activities in Yeast . . . . . . . . . . . . . . . . . . . . . . 3 Tatiana Kulakovskaya , Lubov Ryasanova , Vladimir Dmitriev , and Anton Zvonarev 2 Yeast Polyphosphatases PPX1 and PPN1: Properties, Functions, and Localization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 Nadeshda Andreeva , Lidia Lichko , Ludmila Trilisenko , Ivan V. Kulakovskiy , and Tatiana Kulakovskaya 3 Polyphosphate Storage and Function in Acidocalcisomes . . . . . . . . . . . 35 Roberto Docampo 4 Inorganic Polyphosphates in Mycorrhiza . . . . . . . . . . . . . . . . . . . . . . . . . 49 Tatsuhiro Ezawa , Chiharu Tani , Nowaki Hijikata , and Yusuke Kikuchi 5 Functions of Inositol Polyphosphate and Inorganic Polyphosphate in Yeast and Amoeba . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61 Adolfo Saiardi Part II Higher Eukaryotes 6 Methods of Inorganic Polyphosphate (PolyP) Assay in Higher Eukaryotic Cells . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81 Maria E. Solesio and Evgeny V. Pavlov 7 Inorganic Polyphosphates in the Mitochondria of Mammalian Cells . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91 Lea K. Seidlmayer and Elena N. Dedkova 8 Role of Inorganic Polyphosphate in the Cells of the Mammalian Brain . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115 Artyom Y. Baev , Plamena R. Angelova , and Andrey Y. Abramov vii viii Contents 9 Inorganic Polyphosphate Functions and Metabolism in Insects . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 123 Fabio Mendonça Gomes , I. B. Ramos , H. Araujo , K. Miranda , and E. A. Ednildo 10 Inorganic Polyphosphate and Its Chain- Length Dependency in Tissue Regeneration Including Bone Remodeling and Teeth Whitening . . . . . . . . . . . . . . . . 139 Toshikazu Shiba 11 Inorganic Polyphosphate in Blood Coagulation. . . . . . . . . . . . . . . . . . . 159 Stephanie A. Smith and James H. Morrissey 12 Influence of Condensed Phosphates on the Physical Chemistry of Calcium Phosphate Solids . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 177 Sidney Omelon and Wouter Habraken 13 Inorganic Polyphosphate Is an Essential Structural and Functional Component of the Mammalian Ion Channel TRPM8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 207 Eleonora Zakharian 14 Inorganic Polyphosphate in Tissue Engineering . . . . . . . . . . . . . . . . . . 217 Rahul Gawri , Jean-Philippe St-Pierre , Robert Pilliar , Marc Grynpas , and Rita A. Kandel Conclusion: Evolution of the Polyphosphate Role in Eukaryotes . . . . . . . . 241 Part I Lower Eukaryotes 1 The Role of Inorganic Polyphosphates in Stress Response and Regulation of Enzyme Activities in Yeast Tatiana Kulakovskaya , Lubov Ryasanova , Vladimir Dmitriev , and Anton Zvonarev Abstract Inorganic polyphosphates (polyPs) are multifunctional compounds involved in adap- tation of microorganisms to stress. In yeast, polyPs serve a reserve of phosphorus that is consumed by cells with phosphate defi ciency. Under phosphate excess, polyP bio- synthesis regulates the intracellular phosphate concentration. PolyPs accumulate under conditions of growth suppression under nitrogen starvation and heavy metal toxic stress, and also upon the adaptation of yeast to a hydrophobic carbon source. The participation of polyPs in the regulation of enzyme activities is discussed. 1.1 Introduction I norganic polyphosphates (polyPs) are linear polymers containing a few to several hundred orthophosphate residues linked by energy-rich phosphoanhydride bonds (Fig. 1 .1 ). Until recently they were considered molecular fossils, ATP precursors in evolution, and a phosphorus storage mechanism in microorganisms. Igor Kulaev, a pioneer in polyP biochemistry, suggested multiple roles for these polymers in the regulation of cellular processes because of the ability to form complexes with metal ions, proteins, and RNA (Kulaev 1 979) . The interaction of negatively charged pol- yPs with anionic biopolymers, such as poly-beta hydroxybutyrate (Reusch 1992 ) and probably RNA (Kulaev 1 979 ), is mediated by divalent metal cations. T. Kulakovskaya (*) Laboratory of Regulation of Biochemical Processes , Skryabin Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences , Pushchino , Moscow Region 142290 , Russia e-mail: [email protected] L. Ryasanova (cid:129) V. Dmitriev (cid:129) A. Zvonarev Skryabin Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences, Pushchino , Moscow Region 142290 , Russia © Springer International Publishing Switzerland 2016 3 T. Kulakovskaya et al. (eds.), Inorganic Polyphosphates in Eukaryotic Cells, DOI 10.1007/978-3-319-41073-9_1 4 T. Kulakovskaya et al. Fig. 1.1 Structure of linear inorganic polyphosphate (polyP) The excellent studies of Arthur Kornberg and co-workers demonstrated the essential role of polyPs in the switching of gene expression and in cell survival in the stationary phase and under stress (Kornberg 1 995; Rao et al. 2009) . PolyP and polyphosphate kinase participate in induction of the synthesis of RpoS, an RNA- polymerase subunit in bacteria that is responsible for expression of the genes involved in the stationary phase and adaptation to stress; it is also involved in bacte- rial cell motility, biofi lm formation, and virulence (Rao et al. 2 009 ). The adaptation of E scherichia coli to amino acid starvation is a remarkable exam- ple of polyP involvement in the response to stress (Rao et al. 2009 ). This process is mediated by guanosine 5′-triphosphate, 3′-diphosphate (pppGpp) and guanosine 5′-diphosphate, 3′-diphosphate (ppGpp), the so-called alarmones. These compounds enhance the expression of many stress-induced genes (Magnusson et al. 2 005 ; Sharma and Chatterji 2 010 ). The increase of concentrations of (p)ppGpp in E . coli cells enhances the degradation of polyPs by polyphosphatases ppx and gppA (Kuroda 2006) . The gppA enzyme also catalyzes the degradation of p(ppGpp) (Keasling et al. 1993 ). As a result, the polyP content in E. coli increases many fold under amino acid starvation. PolyP forms a complex with ATP-dependent Lon proteinase and increases its activity (Kuroda 2 006) . These polyPs, with an average chain length of 65–700 phosphate residues, bind up to four Lon molecules per one polyP chain, and such a complex is responsible for the proteolysis of ribosomal proteins (Kuroda 2 006 ). The resulting free amino acids are used for biosynthesis of inducible amino acid trans- porters and enzymes of amino acid biosynthesis. The mechanisms of polyP participation in stress response in eukaryotic microor- ganisms are not yet well understood. However, many facts suggest the involvement of polyP in the adaptive mechanisms in fungi: (cid:129) The polyP content and chain length are strongly dependent on the growth stage and conditions (cid:129) P olyP was found in vacuoles, cytoplasm, cell wall, nuclei, and mitochondria by both subcellular fractionation methods and various microscopic techniques (cid:129) The cell compartments possess specifi c enzymes of polyP metabolism, differ- ently affecting by environmental conditions T his chapter considers changes in polyP content and chain length under various stresses and the involvement of polyP in the regulation of enzyme activities in yeast. 1.2 P Limitation and Excess i PolyP content in the cells of S accharomyces cerevisiae strongly depends on the culture medium composition and the growth stage (Vagabov et al. 1 998 , 2000) . The polyP pool of yeast is heterogenic: traditionally fi ve polyP fractions were isolated from S . cerevisiae