Brewing Microbiology
Managing Microbes, Ensuring Quality and Valorising Waste
- 2nd Edition - January 20, 2025
- Editor: Annie Hill
- Language: English
- Hardback ISBN:9 7 8 - 0 - 3 2 3 - 9 9 6 0 6 - 8
- eBook ISBN:9 7 8 - 0 - 3 2 3 - 9 9 6 0 7 - 5
Brewing Microbiology: Managing Microbes, Ensuring Quality and Valorising Waste, Second Edition covers micro-organisms of significance to the brewing industry, including the most… Read more
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Request a sales quoteBrewing Microbiology: Managing Microbes, Ensuring Quality and Valorising Waste, Second Edition covers micro-organisms of significance to the brewing industry, including the most recent threats to beer quality and stability that have emerged. Reflecting the significant surge in production of no- and low-alcohol (NOLO) beers and Hard Seltzers since the publication of the 1st edition, and the lack of information available on the increased microbiological risk associated with these beverages – and how to control them, a new chapter "Maintaining microbiological quality control in Hard Seltzers and NOLO beverages" provides best practices in ensuring safe and effective management in production and stability. Sustainability and the environment have been at the forefront of brewers strategic thinking for many years. The first edition of Brewing Microbiology included coverage of anaerobic treatments of brewery waste and waste-water treatment. This section has been expanded to cover recent innovations in the valorization of brewery waste streams, such as biotransformation of brewers spent grains.
- Provides a fully revised and updated resource, including the latest developments in brewing microbiology and its role in quality and safety assurance
- Discusses the microbes that are essential for successful beer production and processing
- Covers spoilage bacteria, yeasts, sensory quality and microbiological waste management
- Focuses on developments in industry and academia, bringing together leading experts in the field
- Title of Book
- Cover image
- Title page
- Table of Contents
- Copyright
- Contributors
- Preface
- Introduction to brewing microbiology 2E
- Brewing yeast
- Process and product integrity
- Waste valorisation
- Acknowledgements
- Part I. Yeast: Properties and management
- Chapter 1. Brewing yeasts: An overview
- 1.1 Yeasts
- 1.2 Ale yeasts
- 1.3 Lager yeasts
- 1.4 Non-saccharomyces brewing yeasts
- 1.5 Perspectives
- Chapter 2. Yeast quality assessment, management and culture maintenance
- 2.1 Introduction
- 2.2 Objectives of wort fermentation
- 2.3 Brewer's yeast species
- 2.4 Yeast management
- 2.5 Storage of yeast stock cultures between propagations
- 2.6 Preservation of yeast strains
- 2.7 Yeast propagation
- 2.8 Yeast collection
- 2.9 Yeast storage
- 2.10 Yeast washing
- 2.11 Yeast stress
- 2.12 Dried yeast
- 2.13 Conclusions
- Chapter 3. Theory and practice of fermentation modeling
- 3.1 Introduction
- 3.2 Parameters influencing yeast growth and fermentation of barley malt
- 3.3 Modelling: techniques and applications
- 3.3.1 Modelling fermentations
- 3.3.2 Logistic models
- 3.3.3 The incomplete β-function
- 3.3.4 Additional models
- 3.3.5 Application of models
- 3.4 Advanced fermentation techniques
- 3.5 Future trends and sources for further information
- 3.6 Closing remarks
- Chapter 4. Advances in metabolic engineering of yeasts
- 4.1 Introduction
- 4.2 Metabolic engineering
- 4.3 Tools for metabolic engineering
- 4.4 Strategies for metabolic engineering
- 4.5 Brewing yeast genetics
- 4.6 Metabolic engineering and the complexities of metabolic regulation
- 4.7 Impact of brewing yeast population dynamics
- 4.8 Targets for engineering of brewing yeast
- 4.9 Future perspective
- 4.10 Further sources of further information
- Chapter 5. Yeast identification and characterisation
- 5.1 Biodiversity and characterisation of yeast species and strains from a brewing environment
- 5.2 Microbiological, physiological, identification and typing methods
- 5.2.1 Differences in top- and bottom-fermenting brewing yeast strains
- 5.2.2 Overview of identification methods
- 5.2.3 Selection of successful standard and recently introduced methods
- 5.2.4 Promising new methods
- 5.3 Brewing yeast cell count/viability/vitality methods
- 5.3.1 Cell-counting methods
- 5.3.2 Viability methods
- 5.3.3 Vitality methods
- 5.4 Monitoring yeast and fermentation
- 5.4.1 Wort and yeast specifications
- 5.4.2 Monitoring of fermentation and maturation parameters and their application with yeast
- Part II. Spoilage bacteria and other contaminants
- Chapter 6. Toxigenic fungi and mycotoxins in the barley-to-beer chain
- 6.1 Introduction
- 6.2 Barley malt: A key raw material in brewing
- 6.3 Evolution of fungi in the barley–malt ecosystem
- 6.4 Impacts of barley-associated fungi on malt quality
- 6.5 Aspergillus, Penicillium and Fusarium mycotoxins
- 6.5.1 Aflatoxins
- 6.5.2 Ochratoxin A
- 6.5.3 Fusarium toxins
- 6.6 Fate of mycotoxins in the barley-to-beer chain
- 6.6.1 Mycotoxins in barley and malting
- 6.6.2 Mycotoxins in brewing and beer
- 6.6.3 Mycotoxins in by-products
- 6.7 Regulation of mycotoxins in Europe
- 6.8 Emerging mycotoxin issues
- 6.8.1 Modified mycotoxins
- 6.8.2 Enniatins and beauvericin
- 6.9 Preventive actions
- 6.9.1 Pre-harvest management
- 6.9.2 Post-harvest management
- 6.9.3 Mitigation measures during processing
- 6.9.4 Sampling and on-site mycotoxin detection methods
- 6.10 Future trends
- 6.11 Sources of further information and advice
- Chapter 7. Gram-positive spoilage bacteria in brewing
- 7.1 Introduction
- 7.2 Beer-spoilage LAB
- 7.2.1 Historical backgrounds and taxonomy
- 7.2.2 General features of beer-spoilage LAB
- 7.2.3 Association of beer-spoilage LAB with their habitat
- 7.2.4 Factors affecting the growth of LAB in beer
- 7.2.5 Probiotic potential of beer-spoilage LAB
- 7.3 Hop tolerance mechanisms in beer-spoilage LAB
- 7.3.1 Antibacterial effects of hop bitter acids
- 7.3.2 Hop tolerance mechanisms associated with cytoplasmic membrane
- 7.3.3 Hop tolerance mechanisms associated with cell wall
- 7.3.4 Other hop tolerance mechanisms
- 7.3.5 Hop tolerance genes and their distribution in beer-spoilage LAB
- 7.3.6 Hypothetical origin of beer-spoilage LAB
- 7.4 Culture and preservation methods for beer-spoilage LAB
- 7.4.1 Stability of hop tolerance ability
- 7.4.2 Stability of hop tolerance genes
- 7.4.3 Culturability of beer-spoilage LAB
- 7.4.4 Subculture and preservation methods of beer-spoilage LAB
- 7.5 Identification of emerging beer-spoilage LAB in the brewing industry
- 7.5.1 Species-specific PCR for beer-spoilage LAB detection and identification method
- 7.5.2 Species-independent PCR for beer-spoilage LAB detection and identification method
- 7.5.3 Third-generation DNA sequencing technology-based method for comprehensive detection and identification of beer-spoilage bacteria
- 7.6 Other Gram-positive bacteria in brewing
- 7.6.1 Brewery-related LAB other than Lactobacillus and Pediococcus
- 7.6.2 Endospore-forming bacteria
- 7.6.3 Other Gram-positive bacteria relevant in brewing
- 7.7 Concluding remarks
- Chapter 8. Gram-negative spoilage bacteria in brewing
- 8.1 Introduction: Gram-negative bacteria in brewing
- 8.2 Acetic acid bacteria
- 8.2.1 Taxonomic status of brewery-related AAB
- 8.2.2 Metabolic aspects of AAB
- 8.2.3 Occurrence and beer spoilage by AAB
- 8.2.4 Detection of AAB
- 8.3 Zymomonas
- 8.3.1 Taxonomic status of Zymomonas
- 8.3.2 Occurrence and beer spoilage ability of Zymomonas
- 8.3.3 Metabolic aspects of Zymomonas
- 8.3.4 Detection of Zymomonas
- 8.4 Brewery-related Enterobacteriaceae
- 8.4.1 Obesumbacterium proteus/Shimwellia pseudoproteus
- 8.4.2 Coliform bacteria related to brewing environments
- 8.4.3 Detection of Enterobacteriaceae in brewery environments
- 8.5 Conclusions
- Chapter 9. Strictly anaerobic beer-spoilage bacteria
- 9.1 Introduction
- 9.2 The types of strictly anaerobic beer-spoilage bacteria
- 9.2.1 Pectinatus
- 9.2.2 Megasphaera
- 9.2.3 Selenomonas and Propionispira (Zymophilus)
- 9.2.4 Prevotella
- 9.3 Occurrence in artificial and natural environments
- 9.3.1 Pectinatus
- 9.3.2 Megasphaera
- 9.3.3 Selenomonas and Propionispira
- 9.3.4 Prevotella
- 9.4 Appearance of cells and laboratory cultures
- 9.4.1 Pectinatus
- 9.4.2 Megasphaera
- 9.4.3 Selenomonas and Propionispira
- 9.4.4 Prevotella
- 9.5 General physiology and metabolism
- 9.5.1 Pectinatus
- 9.5.2 Megasphaera
- 9.5.3 Selenomonas and Propionispira
- 9.5.4 Prevotella
- 9.6 Growth and effects in beer
- 9.6.1 Pectinatus
- 9.6.2 Megasphaera
- 9.6.3 Selenomonas and Propionispira
- 9.6.4 Prevotella
- 9.7 Management of contaminations
- 9.7.1 Prevention
- 9.7.2 Elimination
- 9.8 Future outlook and research needs
- 9.9 Sources of further information and advice
- Part III. Reducing microbial spoilage: Design and technology
- Chapter 10. Hygienic design and cleaning-in-place (CIP) systems in breweries
- 10.1 Introduction
- 10.2 Brewery contamination
- 10.2.1 Beer is a hostile environment
- 10.2.2 Types of contamination recognised in the brewery
- 10.2.3 The prevalence of microorganisms in the brewery
- 10.3 The main principles of hygienic design as applied in the brewery
- 10.3.1 Brewery pipework design and layout to minimise contamination
- 10.3.2 Operating conditions required to achieve a cleaning action in pipework
- 10.3.3 Hygienic design and operating practice of valves, fixtures and fittings
- 10.3.4 The effect of material surface finish on microbial surface adhesion
- 10.4 An overview of cleaning-in-place systems used in the brewery
- 10.4.1 Operating conditions of a Cleaning-In-Place system in the brewery
- 10.4.2 Types of Cleaning-In-Place systems recognised across the brewery
- 10.4.2.1 Single use
- 10.4.2.2 Partial and full recovery cleaning system
- 10.4.3 Cleaning-In-Place fluid composition
- 10.4.3.1 Detergents
- 10.4.3.2 Steriliant
- 10.4.4 Evaluation of the effectiveness of Cleaning-In-Place systems
- 10.5 Conclusions
- 10.6 Commentary/future trends
- 10.6.1 Future brewery designs and the impact on water and energy recovery
- 10.6.2 Developments in nanotechnology to provide antimicrobial surfaces and materials
- 10.6.3 Developments in data-driven approaches to cleaning
- 10.7 Further information and advice
- Chapter 11. Reducing microbial spoilage of beer using filtration
- 11.1 Introduction
- 11.2 Filtration technologies in brewing
- 11.3 Filter aid filtration
- 11.4 Crossflow microfiltration
- 11.5 Sterile filtration
- 11.5.1 Cartridge filtration
- 11.5.2 Integrity testing
- 11.5.3 Other sterile filters
- 11.5.4 Downstream process
- 11.6 Improving filtration performance
- 11.6.1 Centrifugation
- 11.6.2 Flocculants (finings)
- 11.6.3 Enzyme treatments
- 11.7 Future trends
- 11.8 Sources of further information and advice
- Chapter 12. Reducing microbial spoilage of beer using pasteurisation
- 12.1 Introduction
- 12.2 History
- 12.3 Principles of pasteurisation
- 12.4 D value, z value, P value, process time, pasteurisation units and L value
- 12.5 Spoilage hurdles
- 12.5.1 Ethanol
- 12.5.2 Low pH
- 12.5.3 Hop resins
- 12.5.4 Carbon dioxide
- 12.5.5 Low oxygen level
- 12.5.6 Low nutrient content
- 12.6 Microorganism heat resistance
- 12.7 Tunnel pasteurisation
- 12.7.1 Cleaning
- 12.8 Flash pasteurisation
- 12.8.1 Process control
- 12.8.2 Gas breakout
- 12.8.3 Plate failure
- 12.9 Flavour change
- 12.10 Good practice and quality control
- 12.10.1 Microbiological problems
- 12.11 Future trends
- 12.12 Sources of further information and advice
- Chapter 13. Maintaining microbiological quality control in NOLO beverages and hard seltzers
- 13.1 Production of LAB, AFB and hard seltzers
- 13.1.1 LAB and AFB
- 13.1.2 Production of hard seltzers
- 13.2 Characteristics of LABs, AFBs and hard seltzers
- 13.3 Spoilage risk in LABs, AFBs and hard seltzers
- 13.4 Potential spoilers of LABs, AFBs and hard seltzers
- 13.4.1 Enterobacteriaceae
- 13.4.2 Clostridium
- 13.4.3 Bacillus, Brevibacillus and Paenibacillus
- 13.4.4 Listeria and Staphylococcus
- 13.4.5 Leuconostoc and Oenococcus
- 13.5 Mitigating against spoilage of LABs, AFBs and hard seltzers
- 13.6 Conclusions and future considerations
- Chapter 14. Traditional methods of detection and identification of brewery spoilage organisms
- 14.1 Detection of brewery spoilage organisms
- 14.1.1 Raw materials
- 14.1.1.1 Cereals
- 14.1.1.2 Water
- 14.1.1.3 Yeast
- 14.1.1.4 Hops
- 14.1.1.5 Sugars and syrups
- 14.1.2 Brewing process
- 14.1.2.1 Brewery surfaces
- 14.1.2.2 Air and process gases
- 14.1.2.3 Wort
- 14.1.2.4 Fermentation
- 14.1.3 Product
- 14.1.3.1 Bright beer
- 14.1.3.2 Packaging
- 14.1.3.3 Dispense
- 14.2 Identification of brewing spoilage organisms
- 14.3 Summary
- Chapter 15. Rapid detection and identification of spoilage microorganisms in beer
- 15.1 Introduction
- 15.2 Cell-based methods
- 15.2.1 Hygiene tests (ATP bioluminescence, oxidoreductase)
- 15.2.2 Fluorescence microscopy and cytometry
- 15.2.3 MALDI-TOF mass spectrometry
- 15.2.4 Surface enhanced Raman spectroscopy
- 15.2.5 Biosensors
- 15.3 Nucleic-acid based methods
- 15.3.1 Polymerase chain reaction
- 15.3.1.1 Primer design
- 15.3.1.2 Endpoint PCR
- 15.3.1.3 Real-time or quantitative PCR
- 15.3.1.4 Multiplex PCR
- 15.3.1.5 Nested PCR
- 15.3.1.6 Loop-mediated isothermal amplification
- 15.3.1.7 RT-PCR
- 15.3.1.8 Differentiation between viable and nonviable cells
- 15.3.2 In situ hybridisation detection systems
- 15.3.3 DNA Microarrays
- 15.3.4 Sequencing
- 15.4 Emerging technologies
- 15.5 Conclusions
- Chapter 16. Beer packaging: Microbiological–hazards and considerations
- 16.1 Introduction
- 16.2 Microbiological hazards in the filling hall
- 16.2.1 Filling machine
- 16.2.1.1 Filler design
- 16.2.1.2 Process steps in the filling machine
- 16.2.1.3 Media transport
- 16.2.1.4 Filling process
- 16.2.1.5 Transfer to closing machine
- 16.2.2 Closing machine
- 16.2.3 Packaging material
- 16.2.3.1 Nonreturnable bottles
- 16.2.3.2 Returnable bottles
- 16.2.3.3 Cans
- 16.2.3.4 Plastic bottles
- 16.2.3.5 Kegs
- 16.2.3.6 Other containers
- 16.2.3.7 Closures
- 16.2.3.8 Other packaging aids
- 16.2.4 Water
- 16.2.5 Air
- 16.2.6 Carbon dioxide
- 16.2.7 Environment
- 16.3 Biofilm growth in the packaging hall
- 16.4 Minimisation of risks
- 16.4.1 General
- 16.4.2 Cleaning and sanitation
- 16.4.3 Ultraclean filling
- 16.5 Future trends
- Chapter 17. Draught beer: Hygiene, microbiology and quality
- 17.1 Introduction
- 17.1.1 Global beer market
- 17.1.2 Draught beer market
- 17.1.3 Beer dispense
- 17.2 Draught beer: hygiene
- 17.2.1 Line cleaning
- 17.2.2 Line composition
- 17.2.3 Keg contamination (couplers+FOB)
- 17.2.4 Taps and nozzles
- 17.2.5 Temperature
- 17.2.6 Throughput
- 17.3 Draught beer: microbiology
- 17.3.1 Spoilage
- 17.3.2 Biofilms
- 17.3.3 Microbiota
- 17.4 Draught beer: quality
- 17.4.1 Consumers
- 17.4.2 Microbiological testing
- 17.4.3 Forcing
- 17.4.4 Trade quality
- 17.4.5 Impact of best hygienic practice
- 17.5 Other draught beverages
- 17.5.1 Alcohol-free beers
- 17.5.2 Cider
- 17.6 Improving quality
- 17.6.1 Low hanging fruit
- 17.6.2 Step change
- 17.6.3 Cultural change
- Part IV. Impact of microbiology on sensory quality
- Chapter 18. Biotransformation of wort components for appearance, flavour and health
- 18.1 Introduction
- 18.2 Impact of yeast on beer appearance
- 18.3 Impact of yeast on beer flavour
- 18.3.1 Impact of yeast on beer taste
- 18.3.2 Impact of yeast on beer aroma
- 18.3.2.1 Alcohols
- 18.3.2.2 Aldehydes
- 18.3.2.3 Acids
- 18.3.2.4 Esters
- 18.3.2.5 Ketones
- 18.3.2.6 Volatile phenolic compounds
- 18.3.2.7 Terpenoids
- 18.3.2.8 Volatile sulphur compounds
- 18.4 Impact of bacteria on beer appearance and flavour
- 18.5 Impact of yeast on the health properties of beer
- 18.6 Impact of bacteria on the health properties of beer
- 18.7 Future trends
- 18.8 Further information
- Chapter 19. Sensory analysis as a tool for microbial quality control in the brewery
- 19.1 Introduction
- 19.2 Part 1: Microbes, flavours, novel flavour profiles, off-flavours and taints in brewing
- 19.2.1 Microbial spoilage overview
- 19.2.2 Off-flavours and off-odours
- 19.2.3 Taints and off-flavours
- 19.2.4 Air, water, minerals and raw materials
- 19.3 The microbiology of ‘atypical flavour’ production in brewing—An overview
- 19.3.1 Moulds—Additional factors for consideration
- 19.3.2 Beer and wort—Overview, with some sensory evaluation considerations
- 19.3.3 Beer wort spoiling bacteria
- 19.3.4 Beer spoiling bacteria
- 19.3.5 Beer spoiling yeast—An early broad introduction
- 19.4 Speciality beer production and processes
- 19.4.1 Biological acidification
- 19.4.2 Speciality beers—Wheat beers
- 19.4.3 Speciality beers—Berliner Weisse
- 19.4.4 Speciality beers—Sour beers—An introduction
- 19.4.5 Speciality beers—Brett beers—And introducing phenolic off-flavour
- 19.4.6 Speciality beers—Lambic and gueuze
- 19.4.7 Speciality beers—Wood and barrel-aged beers
- 19.4.8 Pasteurisation, dry hopping and introducing bottle conditioning
- 19.5 New developments in the uses and applications of microorganisms for flavourful beer production: Strains and hybrids as used in pure culture or within in-sequence fermentations
- 19.5.1 Introduction—A wild world of fermentation
- 19.5.1.1 Saccharomyces or non-Saccharomyces?—Of yeasts, alternate yeast species, hybrids, mutants and genomic variation
- 19.5.1.2 Species hybridisation—Seeking desired traits for flavour production
- 19.5.1.3 The taming of the yeasts and bioprospecting
- 19.5.1.4 Beer fermented with yeasts more commonly associated with other fermented beverages
- 19.5.1.5 Of species, strains and flavour tales. A brief listing of some key alternate brewery fermentative yeasts
- 19.5.2 Non- and low-alcoholic beers
- 19.5.3 The problem with diacetyl—Avoiding buttery beers and the situation with dry hopping and yeast-based bio-transformations
- 19.5.4 Lambic beers
- 19.5.5 Brettanomyces—Organisms with multiple complex roles to play
- 19.5.6 Coolships, blending and bottle conditioning/refermentation
- 19.5.7 Barrel ageing: Sorting out some issues with the use of wood
- 19.5.8 Ending on a sour note: As beer goes sour by intention. A bio-prospecting addendum note and a resounding summation
- 19.6 Conclusion—Part 1
- 19.7 Part 2: Sensory evaluation
- 19.7.1 Getting started with sensory
- 19.7.2 Creating an effective sensory team
- 19.7.3 New panelists
- 19.7.4 Building a vocabulary
- 19.7.5 Brand profiles
- 19.8 Raw materials
- 19.9 Gathering data for sensory evaluation
- 19.9.1 Paper or electronic?
- 19.9.2 Presenting sensory panel data
- 19.9.3 Shelf-life evaluation
- 19.9.4 Proactive sensory
- 19.9.5 Sensory training
- 19.10 Conclusion—Part 2
- Part V. The recycling and valorisation of brewing residues
- Chapter 20. Anaerobic treatment of brewery wastes
- 20.1 Introduction
- 20.2 Key factors affecting the anaerobic digestion process
- 20.2.1 Organic content
- 20.2.2 Nutrients
- 20.2.3 pH and alkalinity
- 20.2.4 Temperature
- 20.2.5 Solid and hydraulic retention times
- 20.2.6 Organic loading rate
- 20.2.7 Toxic compounds
- 20.2.8 Treatment configuration: Single- and multi-stage systems
- 20.3 Factors affecting the application of anaerobic digestion in waste treatment
- 20.3.1 Pre-treatment of wastes
- 20.3.2 Co-digestion
- 20.3.3 Technology selection
- 20.3.4 Biogas production and use
- 20.3.5 Digestate handling and disposal
- 20.4 Anaerobic treatment of brewery wastes
- 20.4.1 Waste production and collection
- 20.4.2 Constituents of wastes
- 20.4.3 Treatment and pre-treatment requirements
- 20.4.4 Co-digestion
- 20.4.5 Biogas production
- 20.4.6 Digestate management
- 20.5 Conclusion and perspectives
- Chapter 21. Water treatment and reuse in breweries
- 21.1 Introduction
- 21.2 Production and composition of brewery wastewater
- 21.3 Pre-treatment of brewery wastewater
- 21.3.1 Physical pre-treatment methods
- 21.3.2 Chemical pre-treatment methods
- 21.3.3 Biological pre-treatment methods
- 21.4 Advanced treatment of brewery wastewater
- 21.4.1 Membrane filtration technologies
- 21.4.2 Membrane bioreactor technologies
- 21.4.3 Electrochemical technologies
- 21.4.4 Microbial fuel cell technologies
- 21.4.5 Electric discharge plasma technologies
- 21.5 Challenges and future prospects
- 21.6 Conclusions
- Index
- No. of pages: 446
- Language: English
- Edition: 2
- Published: January 20, 2025
- Imprint: Woodhead Publishing
- Hardback ISBN: 9780323996068
- eBook ISBN: 9780323996075
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