《英语教学》（英文版）9 Restriction Endonucleases

Molecular Biology Problem Solver: A Laboratory Guide. Edited by Alan S Gerstein ISBNS:0-471-37972-7( Paper);0-471 (Electronic) 9 Restriction endonucleases Derek Robinson, Paul R. Walsh, and joseph A. Bonventre Background Information 226 Which Restriction Enzymes Are Commercially Why Are Some Enzymes More Expensive Than Others? 227 What Can You do to reduce the cost of Working with Restriction Enzymes? If You Could Select among Several Restriction Enzymes for Your Application, What Criteria Should You Consider to Make the Most Appropriate Choice? 229 What Are the General Properties of Restriction Endonucleases? 232 What Insight Is Provided by a Restriction Enzyme's Quality Control data? .233 How Stable Are Restriction Enzymes How Stable Are Diluted Restriction Enzymes 236 Simple Digests How Should You Set up a Simple Restriction Digest?... 236 ls It Wise to Modify the Suggested Reaction Conditions? 237 Complex Restriction Dige Should You Alter the Reaction Volume and DNAst...239 How Can a Substrate Affect the restriction Dige Concentration? ...24 Double Digests: Simultaneous or Sequential? 225

225 9 Restriction Endonucleases Derek Robinson, Paul R. Walsh, and Joseph A. Bonventre Background Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 226 Which Restriction Enzymes Are Commercially Available? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 226 Why Are Some Enzymes More Expensive Than Others? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 227 What Can You Do to Reduce the Cost of Working with Restriction Enzymes? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 228 If You Could Select among Several Restriction Enzymes for Your Application, What Criteria Should You Consider to Make the Most Appropriate Choice? . . . . . . . . . . . . . . 229 What Are the General Properties of Restriction Endonucleases? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 232 What Insight Is Provided by a Restriction Enzyme’s Quality Control Data? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 233 How Stable Are Restriction Enzymes? . . . . . . . . . . . . . . . . . . 236 How Stable Are Diluted Restriction Enzymes? . . . . . . . . . . . 236 Simple Digests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 236 How Should You Set up a Simple Restriction Digest? . . . . . 236 Is It Wise to Modify the Suggested Reaction Conditions? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 237 Complex Restriction Digestions . . . . . . . . . . . . . . . . . . . . . . . . . 239 How Can a Substrate Affect the Restriction Digest? . . . . . 239 Should You Alter the Reaction Volume and DNA Concentration? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 241 Double Digests: Simultaneous or Sequential? . . . . . . . . . . . . 242 Molecular Biology Problem Solver: A Laboratory Guide. Edited by Alan S. Gerstein Copyright © 2001 by Wiley-Liss, Inc. ISBNs: 0-471-37972-7 (Paper); 0-471-22390-5 (Electronic)

Genomic Digests When Preparing Genomic DNA for Southern Blotting, How Can You Determine If Complete Digestion Has Been Obtained? 244 What Are Your Options If You Must Create Additional Rare or Unique Restriction Sites? 247 Troubleshooting∴. 255 What Can Cause a Simple Restriction Digest to Fail? 255 The Volume of Enzyme in the Vial Appears Very Low. Did eakage Occur during Shipment The Enzyme Shipment Sat on the Shipping Dock for Analyzing Transformation Failure and Other Multiple-Step procedures Involving Restriction Enzymes 260 Bibliography .262 BACKGROUND INFORMATION Molecular biologists routinely use restriction enzymes as ke eagents for a variety of applications including genomic mapping, restriction fragment length polymorphism(RFLP)analysis, DNA sequencing, and a host of recombinant DNA methodologies. Few would argue that these enzymes are not indispensable tools for the variety of techniques used in the manipulation of DNA, but like many common tools that are easy to use, they are not always applied as efficiently and effectively as possible. This chapter focuses on the biochemical attributes and requirements of re striction enzymes and delivers strategies to optimize their use in mple and complex reactions Which Restriction Enzymes Are Commercially Available? While as many as six to eight types of restriction endonucleases have been described in the literature Class li restriction endonu cleases are the best known, commercially available and the most useful. These enzymes recognize specific DNA sequences cleave each DNA strand to generate termini with 5 phosphate and 3 hydroxyl groups. For the vast majority of enzymes charac- terized to date within this class, the recognition sequence is nor mally four to eight base pairs in length and palindromic. The point of cleavage is within the recognition sequence. A variation on th theme appears in the case of Class IIS restriction endonucleases. 226 Robinson et al

Genomic Digests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 244 When Preparing Genomic DNA for Southern Blotting, How Can You Determine If Complete Digestion Has Been Obtained? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 244 What Are Your Options If You Must Create Additional Rare or Unique Restriction Sites? . . . . . . . . . . . . . . . . . . . 247 Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 255 What Can Cause a Simple Restriction Digest to Fail? . . . . 255 The Volume of Enzyme in the Vial Appears Very Low. Did Leakage Occur during Shipment? . . . . . . . . . . . . . . . . . . . . 259 The Enzyme Shipment Sat on the Shipping Dock for Two Days. Is It still Active? . . . . . . . . . . . . . . . . . . . . . . . . . 259 Analyzing Transformation Failure and Other Multiple-Step Procedures Involving Restriction Enzymes . . . . . . . . . . . . 260 Bibliography . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 262 BACKGROUND INFORMATION Molecular biologists routinely use restriction enzymes as key reagents for a variety of applications including genomic mapping, restriction fragment length polymorphism (RFLP) analysis, DNA sequencing, and a host of recombinant DNA methodologies. Few would argue that these enzymes are not indispensable tools for the variety of techniques used in the manipulation of DNA, but like many common tools that are easy to use, they are not always applied as efficiently and effectively as possible. This chapter focuses on the biochemical attributes and requirements of re￾striction enzymes and delivers strategies to optimize their use in simple and complex reactions. Which Restriction Enzymes Are Commercially Available? While as many as six to eight types of restriction endonucleases have been described in the literature, Class II restriction endonu￾cleases are the best known, commercially available and the most useful. These enzymes recognize specific DNA sequences and cleave each DNA strand to generate termini with 5¢ phosphate and 3¢ hydroxyl groups. For the vast majority of enzymes charac￾terized to date within this class, the recognition sequence is nor￾mally four to eight base pairs in length and palindromic.The point of cleavage is within the recognition sequence. A variation on this theme appears in the case of Class IIS restriction endonucleases. 226 Robinson et al

These recognize nonpalindromic sequences, typically four to seven base pairs in length, and the point of cleavage may vary from within the recognition sequence up to 20 base pairs away (Szybalski et aL., 1991) To date, nearly 250 unique restriction specificities have been discovered(Roberts and Macelis, 2001). New prototype activi- ties are continually being discovered. The Rebase database (http://rebase.neb.comprovidesmonthlyupdatesdetailingnew recognition specificities as well as commercial availability These enzymes naturally occur in thousands of bacterial strains and presumably function as the cells defense against bacterio phage DNA. Nomenclature for restriction enzymes is based on a convention using the first letter of the genus and the first two letters of the species name of the bacteria of origin. For example Sacl and Sacll are derived from Streptomyces achromogenes Of the bacterial strains screened for these enzymes to date, well over two thousand restriction endonucleases have been identified each recognizing a sequence specificity defined by one of the prototype activities. Restriction enzymes isolated from distinct bacterial strains having the same recognition specificity are known as isoschizomers (e.g, SacI and SstI). Isoschizomers that cleave the same DNa sequence at a different position are known as neoschizomers(e.g, Smal and Xmal) Why Are Some Enzymes More Expensive Than Others? The distribution of list prices for any given restriction enzyme can vary among commercial suppliers. This is due to many factors cluding the cost of production, quality assurance, packaging, import duties, and freight. For many commonly available enzymes produced from native overexpressors or recombinant sources, the cost of production is relatively low and is generally a minor factor in the final price. Recombinant enzymes(typically over expressed in a well-characterized E. coli host strain) are often less expensive than their nonrecombinant counterparts due to high yields and the resulting efficiencies in production and purifi cation. In contrast, those enzyme preparations resulting in very low yields are often difficult to purify, and they have significantly higher production costs. In general, these enzymes tend to be dra- matically more expensive (per unit of activity) than those isolated from the more robust sources. As these enzymes may not be avail able at the same unit activity levels of the more common enzymes, they can be less forgiving in nonoptimal reaction conditions, Restriction Endonucleases 227

These recognize nonpalindromic sequences, typically four to seven base pairs in length, and the point of cleavage may vary from within the recognition sequence up to 20 base pairs away (Szybalski et al., 1991). To date, nearly 250 unique restriction specificities have been discovered (Roberts and Macelis, 2001). New prototype activi￾ties are continually being discovered. The REBASE database (http://rebase.neb.com) provides monthly updates detailing new recognition specificities as well as commercial availability. These enzymes naturally occur in thousands of bacterial strains and presumably function as the cell’s defense against bacterio￾phage DNA. Nomenclature for restriction enzymes is based on a convention using the first letter of the genus and the first two letters of the species name of the bacteria of origin. For example, SacI and SacII are derived from Streptomyces achromogenes. Of the bacterial strains screened for these enzymes to date, well over two thousand restriction endonucleases have been identified— each recognizing a sequence specificity defined by one of the prototype activities. Restriction enzymes isolated from distinct bacterial strains having the same recognition specificity are known as isoschizomers (e.g., SacI and SstI). Isoschizomers that cleave the same DNA sequence at a different position are known as neoschizomers (e.g., SmaI and XmaI). Why Are Some Enzymes More Expensive Than Others? The distribution of list prices for any given restriction enzyme can vary among commercial suppliers. This is due to many factors including the cost of production, quality assurance, packaging, import duties, and freight. For many commonly available enzymes produced from native overexpressors or recombinant sources, the cost of production is relatively low and is generally a minor factor in the final price. Recombinant enzymes (typically over￾expressed in a well-characterized E. coli host strain) are often less expensive than their nonrecombinant counterparts due to high yields and the resulting efficiencies in production and purifi- cation. In contrast, those enzyme preparations resulting in very low yields are often difficult to purify, and they have significantly higher production costs. In general, these enzymes tend to be dra￾matically more expensive (per unit of activity) than those isolated from the more robust sources.As these enzymes may not be avail￾able at the same unit activity levels of the more common enzymes, they can be less forgiving in nonoptimal reaction conditions, Restriction Endonucleases 227

and can be more problematic with initial use. The important point is that the relative price of a given restriction enzyme(or isoschizomer) may not be the best barometer of its performance in a specific application or procedure. The enzyme with the highest price does not necessarily guarantee optimal performance; nor does the one with the lowest price consistently translate into the best valu Most commercial suppliers maintain a set of quality assurance standards that each product must pass in order to be approved for release. These standards are typically described in the supplier's product catalogs and detailed in the Certificate of Analysis. When planning to use an enzyme for the first time, it is important to review the corresponding quality control specifications and any usage notes regarding recommended conditions and applications. What Can You Do to Reduce the Cost of working with Restriction Enzymes? Most common restriction enzymes are relatively inexpensiv and often maintain full activity past the designated expiration date. Restriction enzymes of high purity are often stable for many years when stored at -20C. In order to maximize the shelf life of less stable enzymes, many laboratories utilize insulated storage containers to mitigate the effects of freezer temperature fluctua tions. Periodic summary titration of outdated enzymes for activ ity is another way to reduce costs for these reagents. For most applications, 1 ul is used to digest 250ng to l ug of DNA. Enzymes supplied in higher concentrations may be diluted prior to the reac tion in the appropriate storage buffer. A final dilution range of 2000 to 5000 Umits/ml is recommended. However, reducing the amount of enzyme added to the reaction may increase the risk of incomplete digestion with insignificant savings in cost. Dilution is a more practical option when using very expensive enzymes, when sample DNA concentration is below 250ng per reaction, or when partial digestion is required. When planning for partial digestion erial dilution(discussed below) is recommended. Most diluted enzymes should be stable for long periods of time when stored at 20%C. as a rule it is wise to estimate the amount of diluted enzyme required over the next week and prepare the dilution he appropriate storage buffer, accordingly. For immediate use, most restriction enzymes can be diluted in the reaction buffer, kept on ice, and used for the day. Extending the reaction time to greater than one hour can often be used to save enzyme or ensure complete digestion Robinson et al

and can be more problematic with initial use. The important point is that the relative price of a given restriction enzyme (or isoschizomer) may not be the best barometer of its performance in a specific application or procedure.The enzyme with the highest price does not necessarily guarantee optimal performance; nor does the one with the lowest price consistently translate into the best value. Most commercial suppliers maintain a set of quality assurance standards that each product must pass in order to be approved for release.These standards are typically described in the supplier’s product catalogs and detailed in the Certificate of Analysis. When planning to use an enzyme for the first time, it is important to review the corresponding quality control specifications and any usage notes regarding recommended conditions and applications. What Can You Do to Reduce the Cost of Working with Restriction Enzymes? Most common restriction enzymes are relatively inexpensive and often maintain full activity past the designated expiration date. Restriction enzymes of high purity are often stable for many years when stored at -20°C. In order to maximize the shelf life of less stable enzymes, many laboratories utilize insulated storage containers to mitigate the effects of freezer temperature fluctua￾tions. Periodic summary titration of outdated enzymes for activ￾ity is another way to reduce costs for these reagents. For most applications, 1ml is used to digest 250 ng to 1mg of DNA. Enzymes supplied in higher concentrations may be diluted prior to the reac￾tion in the appropriate storage buffer. A final dilution range of 2000 to 5000 Umits/ml is recommended. However, reducing the amount of enzyme added to the reaction may increase the risk of incomplete digestion with insignificant savings in cost. Dilution is a more practical option when using very expensive enzymes, when sample DNA concentration is below 250 ng per reaction, or when partial digestion is required. When planning for partial digestion, serial dilution (discussed below) is recommended. Most diluted enzymes should be stable for long periods of time when stored at -20°C. As a rule it is wise to estimate the amount of diluted enzyme required over the next week and prepare the dilution in the appropriate storage buffer, accordingly. For immediate use, most restriction enzymes can be diluted in the reaction buffer, kept on ice, and used for the day. Extending the reaction time to greater than one hour can often be used to save enzyme or ensure complete digestion. 228 Robinson et al

If You Could Select among Several Restriction Enzymes for Your Application, What Criteria Should You Consider to Make the Most Appropriate Choice? Each restriction endonuclease is a unique enzyme with individ- ual characteristics, which are usually listed in suppliers'catalogs and package inserts. When using an unfamiliar enzyme, these data should be carefully reviewed. In addition some enzymes provide additional activities that may impact the immediate or down- stream application. Ease of Use For many applications it is desirable and convenient to use 1ul per reaction. Most suppliers offer standard enzyme concentrations ranging from 2000 to 20,000 units/ml(2-20 units/ul). In addition many suppliers also offer these enzymes in high concentration (often up to 100,000 units/ml), either as a standard product, or through special order. Enzymes sold at 10 to 20 units/ul are common and usually lend themselves for use in a wider variety of applications. When planning to use enzymes available only in lower concentrations(near 2000 units/ml), be sure to take the final glycerol concentration and reaction volume into account. B following the recommended conditions and maintaining the final glycerol concentration below 5%, you can easily avoid star activit ty. Star Activity When subjected to reaction conditions at the extremes of their operating range, restriction endonucleases are capable of cleaving sequences that are similar, but not identical, to their canonical recognition sequences. This altered specificity has been termed "star activity. Star sites are related to the recognition site, usually differing by one or more bases. The propensity for exhibiting star activity varies considerably among restriction endonucleases. For a given enzyme, star activity will be exhibited at the same relative level in each lot produced, whether isolated from a recombinant or a nonrecombinant source Star activity was first reported for EcoRi incubated in a low ionic strength high pH buffer(Polisky et al., 1975). Under these conditions, while this enzyme would cleave at its canonical site (G/AATTC), it also recognized and cleaved at N/AATTC. This reduced specificity should be a consideration when planning to use a restriction endonuclease in a nonoptimal buffer. It was also found that substituting Mn**for Mg+ can result in star activity Restriction Endonucleases

If You Could Select among Several Restriction Enzymes for Your Application,What Criteria Should You Consider to Make the Most Appropriate Choice? Each restriction endonuclease is a unique enzyme with individ￾ual characteristics, which are usually listed in suppliers’ catalogs and package inserts. When using an unfamiliar enzyme, these data should be carefully reviewed. In addition some enzymes provide additional activities that may impact the immediate or down￾stream application. Ease of Use For many applications it is desirable and convenient to use 1ml per reaction. Most suppliers offer standard enzyme concentrations ranging from 2000 to 20,000 units/ml (2–20 units/ml). In addition many suppliers also offer these enzymes in high concentration (often up to 100,000 units/ml), either as a standard product, or through special order. Enzymes sold at 10 to 20 units/ml are common and usually lend themselves for use in a wider variety of applications. When planning to use enzymes available only in lower concentrations (near 2000 units/ml), be sure to take the final glycerol concentration and reaction volume into account. By following the recommended conditions and maintaining the final glycerol concentration below 5%, you can easily avoid star activity. Star Activity When subjected to reaction conditions at the extremes of their operating range, restriction endonucleases are capable of cleaving sequences that are similar, but not identical, to their canonical recognition sequences. This altered specificity has been termed “star activity.” Star sites are related to the recognition site, usually differing by one or more bases. The propensity for exhibiting star activity varies considerably among restriction endonucleases. For a given enzyme, star activity will be exhibited at the same relative level in each lot produced, whether isolated from a recombinant or a nonrecombinant source. Star activity was first reported for EcoRI incubated in a low ionic strength high pH buffer (Polisky et al., 1975). Under these conditions, while this enzyme would cleave at its canonical site (G/AATTC), it also recognized and cleaved at N/AATTC. This reduced specificity should be a consideration when planning to use a restriction endonuclease in a nonoptimal buffer. It was also found that substituting Mn2+ for Mg2+ can result in star activity Restriction Endonucleases 229

Hsu and Berg, 1978). Prolonged incubation time and high enzyme concentration as well as elevated levels of glycerol and other organic solvents tend to generate star activity (Malyguine Vannier, and Yot, 1980). Maintaining the glycerol concentration to 5% or less is recommended. Since the enzyme is supplied in 50% glycerol, the enzyme added to a reaction should be no more than 10% of the final reaction volume When extra DNA fragments are observed, especially when working with an enzyme for the first time, star activity must be differentiated from partial digestion or contaminating specific endonucleases. first, check to make sure that the reaction condi- tions are well within the optimal range for the enzyme. Then, repeat the digest in parallel reactions, one with twice the activity and one with half the activity of the initial digest. Partial digestion is indicated as the cause when the number of bands is reduced to that expected after repeating the digestion with additional enzyme (or extending incubation time). If extra bands are still evident, contact the supplier's technical support resource for advice. Generally speaking, star activity and contaminating activ ities are more difficult to differentiate Mapping and sequencing he respective cleave es is the best method to distinguish star activity from a partial digest or contaminant activity Site Preference The rate of cleavage at each site within a given DNA substrate can vary(Thomas and Davis, 1975). Fragments containing a subset of sites that are cleaved more slowly than others can result in partial digests containing lighter bands visualized on an ethidium tained agarose gel. Certain enzymes such as Eco Rll require an activator site to allow cleavage(Kruger et al., 1988 ). Substrates lacking the additional site will be cleaved very slowly. For certain enzymes(Nael), adding oligonucleotides containing the site or adding another substrate containing multiple sites can improve utting. In the case of PaeR7l, it has been shown that the sur- rounding sequence can have a profound effect on the cleavage rate(Gingeras and Brooks, 1983). In most cases this rate differ ence is taken in to account because the unit is defined at a point of complete digestion on a standard substrate DNA(e.g, lambda DNA)that contains multiple sites. Problems can arise when certain sites are far more resistant than others, or when highly resistant sites are encountered on substrates other than the stan dard substrate DNA. If a highly resistant site is present in a common cloning vector, then a warning should be noted on the data card or in the catalog Robinson et al

(Hsu and Berg, 1978). Prolonged incubation time and high enzyme concentration as well as elevated levels of glycerol and other organic solvents tend to generate star activity (Malyguine, Vannier, and Yot, 1980). Maintaining the glycerol concentration to 5% or less is recommended. Since the enzyme is supplied in 50% glycerol, the enzyme added to a reaction should be no more than 10% of the final reaction volume. When extra DNA fragments are observed, especially when working with an enzyme for the first time, star activity must be differentiated from partial digestion or contaminating specific endonucleases. First, check to make sure that the reaction condi￾tions are well within the optimal range for the enzyme. Then, repeat the digest in parallel reactions, one with twice the activity and one with half the activity of the initial digest. Partial digestion is indicated as the cause when the number of bands is reduced to that expected after repeating the digestion with additional enzyme (or extending incubation time). If extra bands are still evident, contact the supplier’s technical support resource for advice. Generally speaking, star activity and contaminating activ￾ities are more difficult to differentiate. Mapping and sequencing the respective cleavage sites is the best method to distinguish star activity from a partial digest or contaminant activity. Site Preference The rate of cleavage at each site within a given DNA substrate can vary (Thomas and Davis, 1975). Fragments containing a subset of sites that are cleaved more slowly than others can result in partial digests containing lighter bands visualized on an ethidium stained agarose gel. Certain enzymes such as EcoRII require an activator site to allow cleavage (Kruger et al., 1988). Substrates lacking the additional site will be cleaved very slowly. For certain enzymes (NaeI), adding oligonucleotides containing the site or adding another substrate containing multiple sites can improve cutting. In the case of PaeR7I, it has been shown that the sur￾rounding sequence can have a profound effect on the cleavage rate (Gingeras and Brooks, 1983). In most cases this rate differ￾ence is taken in to account because the unit is defined at a point of complete digestion on a standard substrate DNA (e.g., lambda DNA) that contains multiple sites. Problems can arise when certain sites are far more resistant than others, or when highly resistant sites are encountered on substrates other than the stan￾dard substrate DNA. If a highly resistant site is present in a common cloning vector, then a warning should be noted on the data card or in the catalog. 230 Robinson et al

Methylation Methylation sensitivity can interfere with digestion and cloning eps. Many of the E coli cloning strains express the genes for EcoKI methylase, dam methylase, or dcm methylase. The dam methylase recognizes gatC and methylates at the N6 position of adenine. Mbol recognizes gatC (the same four base-pair sequence as dam methylase) and will only cleave dNa purifie from E coli strains lacking the dam methylase DpnI is one of on a few enzymes known to cleave methylated dNA preferentially, and it will only cleave dNa from dam* strains ( lacks and greer erg, 1977). Another E coli methylase, termed dcm, was found to block AatI and Stul(Song, Rueter, and Geiger, 1988). The dcm methylase recognizes CC(A/T)GG and methylates the second C The restriction enzyme recognition site doesn't have to span the entire methylation site to be blocked. Overlapping methylation sites can cause a problem. An example is the Xbal recognition site 5 TCTAGA 3. Although it lacks the gatC dam methylase or the following 3 bases are TC giving TCTAGATC, then the dam methylase blocks Xbal from cutting. E coli strains with deleted dam and dcm, like GM2163, are commercially available and should be used if the restriction site of interest is blocked by methylation. The first time a methylated plasmid is transformed into GM2163 the number of colonies will be low due to the impor tant role played by dam during replication Methylation problems can also arise when working with mam- malian or plant DNA. DNA from mammalian sources contain C5 methylation at CG sequences. Plant DNA often contains C5 methylation at CG and CNG sequences. Bacterial species contain a wide range of methylation contributed by their restriction mod ification systems(Nelson, Raschke, and McClelland, 1993). Infor mation regarding known sensitivities to methylation can be found on data cards in catalog tables, by searching REBASE, and in the preceding review by Nelson Cloning problems can arise when working with DNA methy lated at the c5 position Most e coli strains have an mcr restric- tion system that cleaves methylated DNA(Raleigh et al., 1988) a strain deficient in this system must be used when cloning DNA from mammalian and plant sources. Substrate effec More on this discussion appears in the question below, How Can a Substrate Affect the Restriction Digest? Restriction Endonucleases 23

Methylation Methylation sensitivity can interfere with digestion and cloning steps. Many of the E. coli cloning strains express the genes for EcoKI methylase, dam methylase, or dcm methylase. The dam methylase recognizes GATC and methylates at the N6 position of adenine. MboI recognizes GATC (the same four base-pair sequence as dam methylase) and will only cleave DNA purified from E. coli strains lacking the dam methylase. DpnI is one of only a few enzymes known to cleave methylated DNA preferentially, and it will only cleave DNA from dam+ strains (Lacks and Green￾berg, 1977). Another E. coli methylase, termed dcm, was found to block AatI and StuI (Song, Rueter, and Geiger, 1988). The dcm methylase recognizes CC(A/T)GG and methylates the second C at the C5 position. The restriction enzyme recognition site doesn’t have to span the entire methylation site to be blocked. Overlapping methylation sites can cause a problem.An example is the XbaI recognition site 5¢ TCTAGA 3¢. Although it lacks the GATC dam methylase target, if the preceding 5¢ two bases are GA giving GATCTAGA or the following 3¢ bases are TC giving TCTAGATC, then the dam methylase blocks XbaI from cutting. E. coli strains with deleted dam and dcm, like GM2163, are commercially available and should be used if the restriction site of interest is blocked by methylation. The first time a methylated plasmid is transformed into GM2163 the number of colonies will be low due to the impor￾tant role played by dam during replication. Methylation problems can also arise when working with mam￾malian or plant DNA. DNA from mammalian sources contain C5 methylation at CG sequences. Plant DNA often contains C5 methylation at CG and CNG sequences. Bacterial species contain a wide range of methylation contributed by their restriction mod￾ification systems (Nelson, Raschke, and McClelland, 1993). Infor￾mation regarding known sensitivities to methylation can be found on data cards in catalog tables, by searching REBASE, and in the preceding review by Nelson. Cloning problems can arise when working with DNA methy￾lated at the C5 position. Most E. coli strains have an mcr restric￾tion system that cleaves methylated DNA (Raleigh et al., 1988). A strain deficient in this system must be used when cloning DNA from mammalian and plant sources. Substrate Effects More on this discussion appears in the question below, How Can a Substrate Affect the Restriction Digest? Restriction Endonucleases 231

WHAT ARE THE GENERAL PROPERTIES OF RESTRICTION ENDONUCLEASES? In general, commercial preparations of restriction endonucle- ases are purified and stored under conditions that ensure optimal nd stability over time; namely -20oC. They are com monly supplied in a solution containing 50% glycerol, Tris buffer, EDTA, salt, and reducing agent. This solution will conveniently remain in liquid form at -20C but will freeze at temperatures below -30%C. Those enzymes shipped on dry ice, or stored at -70oC, will have a white crystalline appearance; they revert to a clear solution as the temperature approaches -20C. As a rule repeated freeze-thaw cycles are not recommended for enzyme solutions because of the possible adverse effects of shearing(more on the question, How Stable are Restriction Enzymes? appears As a group(and by definition), Class II restriction endonucle ases require magnesium(Mg)as a cofactor in order to cleave DNA at their respective recognition sites. Most restriction enzymes are incubated at 37C, but many require higher or lower (i. e, Smal requires incubation at 25C)temperatures. Percent activity tables of thermophilic enzymes incubated at 37 C can be found in some suppliers'catalogs. For most reactions, the pl optima is between 7 and 8 and the NaCl concentration betwee 50 and 100 mM. Concentrated reaction buffers for each enzyme are provided by suppliers. Typically each enzyme is profiled for optimal activity as a function of reaction temperature, pH(buffer ing systems), and salt concentration. Some enzymes are also evaluated in reactions containing additional components(BSA detergents). Generally, these characteristics are documented in the published literature and referenced by suppliers Interestingly, a number of commonly used enzymes can dis broad range of stability and performance characteristics under fairly common reaction conditions. They may vary considerably i activity and may exhibit sensitivity to particular components. In effort to minimize these undesirable effects, suppliers often adjust enzyme buffer components and concentrations to ensure optimal performance for the most common applications. There is a wealth of information about the properties of these enzymes in most suppliers'catalogs, as well as on their Web sites. The documentation supplied with the restriction endonuclease should contain detailed information about the enzymes pro- perties and functional purity. It is important to read the Certifi cate of Analysis when using a restriction enzyme for the first Robinson et al

WHAT ARE THE GENERAL PROPERTIES OF RESTRICTION ENDONUCLEASES? In general, commercial preparations of restriction endonucle￾ases are purified and stored under conditions that ensure optimal reactivity and stability over time; namely -20°C. They are com￾monly supplied in a solution containing 50% glycerol, Tris buffer, EDTA, salt, and reducing agent. This solution will conveniently remain in liquid form at -20°C but will freeze at temperatures below -30°C. Those enzymes shipped on dry ice, or stored at -70°C, will have a white crystalline appearance; they revert to a clear solution as the temperature approaches -20°C. As a rule repeated freeze-thaw cycles are not recommended for enzyme solutions because of the possible adverse effects of shearing (more on the question, How Stable are Restriction Enzymes? appears below). As a group (and by definition), Class II restriction endonucle￾ases require magnesium (Mg2+ ) as a cofactor in order to cleave DNA at their respective recognition sites. Most restriction enzymes are incubated at 37°C, but many require higher or lower (i.e., SmaI requires incubation at 25°C) temperatures. Percent activity tables of thermophilic enzymes incubated at 37°C can be found in some suppliers’ catalogs. For most reactions, the pH optima is between 7 and 8 and the NaCl concentration between 50 and 100 mM. Concentrated reaction buffers for each enzyme are provided by suppliers. Typically each enzyme is profiled for optimal activity as a function of reaction temperature, pH (buffer￾ing systems), and salt concentration. Some enzymes are also evaluated in reactions containing additional components (BSA, detergents). Generally, these characteristics are documented in the published literature and referenced by suppliers. Interestingly, a number of commonly used enzymes can display a broad range of stability and performance characteristics under fairly common reaction conditions. They may vary considerably in activity and may exhibit sensitivity to particular components. In an effort to minimize these undesirable effects, suppliers often adjust enzyme buffer components and concentrations to ensure optimal performance for the most common applications. There is a wealth of information about the properties of these enzymes in most suppliers’ catalogs, as well as on their Web sites. The documentation supplied with the restriction endonuclease should contain detailed information about the enzyme’s pro￾perties and functional purity. It is important to read the Certifi- cate of Analysis when using a restriction enzyme for the first 232 Robinson et al

time, as it may provide important information concerning partic ular substrate DNAs or alternative reaction conditions for a spe cific application What Insight Is Provided by a Restriction Enzyme's Quality Control Data? Restriction enzymes are isolated from bacterial strains that contain a variety of other enzyme activities required for normal cell function. These additional activities include other nucleases phosphatases, and polymerases as well as other dna binding pro- teins that may inhibit restriction enzyme activity In preparations where trace amounts of these activities remain the end-structure of the resulting DNA fragments may be degraded, thus inhibiting subsequent ligation. Likewise plasmid substrates may be nicked thus reducing transformation efficiencies Ideally the restriction enzyme preparation should be purified to homogeneity and free of any detectable activities that might inter fere with digestion or inhibit subsequent reactions planned for the resulting DNA fragments. In order to provide researchers with a practical means to conveniently evaluate the suitability of a given restriction enzyme preparation, suppliers include a Certificate of Analysis with each product, detailing the preparation,s per formance in a defined set of Quality Control Assays. In order to establish a standard reference for the amount of enzyme and sub- strate used in these assays, each supplier must first define the unit substrate and reaction conditions for each product Unit Definition a unit of restriction endonuclease is defined as the amount of zyme required to completely cleave l ug of substrate DNA suS- pended in 50 ul of the recommended reaction buffer in one hour at the recommended assay buffer and temperature. The DNA most often used is bacteriophage Lambda or another well characterized substrate. Note that the unit definition is not based on classic enzyme kinetics. The enzyme molar concentration is in excess. A complete digest is determined by the visualized pattern of cleaved DNA fragments resolved by electrophoresis on an ethidium bromide-stained gel. Some restriction enzymes will behave differently when used outside the parameters of the unit definition. The number of sites(site density)or the particular type of DNA substrate may have an effect on"unit activity, " but it is not always proportional(Fuchs and Blakesley, 1983) Restriction Endonucleases 233

time, as it may provide important information concerning partic￾ular substrate DNAs or alternative reaction conditions for a spe￾cific application. What Insight Is Provided by a Restriction Enzyme’s Quality Control Data? Restriction enzymes are isolated from bacterial strains that contain a variety of other enzyme activities required for normal cell function. These additional activities include other nucleases, phosphatases, and polymerases as well as other DNA binding pro￾teins that may inhibit restriction enzyme activity. In preparations where trace amounts of these activities remain, the end-structure of the resulting DNA fragments may be degraded, thus inhibiting subsequent ligation. Likewise plasmid substrates may be nicked, thus reducing transformation efficiencies. Ideally the restriction enzyme preparation should be purified to homogeneity and free of any detectable activities that might inter￾fere with digestion or inhibit subsequent reactions planned for the resulting DNA fragments. In order to provide researchers with a practical means to conveniently evaluate the suitability of a given restriction enzyme preparation, suppliers include a Certificate of Analysis with each product, detailing the preparation’s per￾formance in a defined set of Quality Control Assays. In order to establish a standard reference for the amount of enzyme and sub￾strate used in these assays, each supplier must first define the unit substrate and reaction conditions for each product. Unit Definition A unit of restriction endonuclease is defined as the amount of enzyme required to completely cleave 1mg of substrate DNA sus￾pended in 50ml of the recommended reaction buffer in one hour at the recommended assay buffer and temperature. The DNA most often used is bacteriophage Lambda or another well￾characterized substrate. Note that the unit definition is not based on classic enzyme kinetics. The enzyme molar concentration is in excess. A complete digest is determined by the visualized pattern of cleaved DNA fragments resolved by electrophoresis on an ethidium bromide-stained gel. Some restriction enzymes will behave differently when used outside the parameters of the unit definition. The number of sites (site density) or the particular type of DNA substrate may have an effect on “unit activity,” but it is not always proportional (Fuchs and Blakesley, 1983). Restriction Endonucleases 233

Quality Control Assays-Maximum Units per Reaction When using procedures requiring larger quantities of enzyme and/or extended reaction times, an appreciation of the quality control data can help determine a safe amount of enzyme for your Overnight Assay Increasing amounts of restriction endonuclease are incubated overnight(typically for 16 hours)in their recommended buffer with l ug of substrate dNa in a volume of 50 ul. The characteris- tic limit digest banding pattern produced by the enzyme in one hour is compared to the pattern produced from an excess of enzyme incubated overnight. A sharp, unaltered pattern under these conditions is an indication that the enzyme preparation is free of detectable levels of nonspecific endonucleases. The maximum number of units yielding an unaltered pattern is eported. Enzymes listing 100 units or more, a 1600-fold over digestion(100 units x 16h), will not degrade DNA up to megabase size in mapping experiments and can be assumed to be virtually free of nonspecific endonuclease (Davis, T. and Robinson, D unpublished observations Nicking Assay Another sensitive test for contaminating endonucleases is a four hour incubation with a supercoiled plasmid that lacks a site for the enzyme being tested. The supercoil is very sensi- tive to nonspecific nicking by a single-stranded endonuclease, cleavage by a double-stranded endonuclease, or topoisomerase activity. If a single-stranded nick occurs, the supercoiled mole- cule. RFl. unwinds and assumes the circular form rFil. If a double-stranded cleavage occurs, the circle will become linear High levels of single-stranded nicking leads to linear DNA All three forms of DNa have distinct electrophoretic mobilities on agarose gels. Enzymes converting 5%or less of the plasmid o relaxed form using 100 units of enzyme for four hours can be considered virtually free of nicking activity. High-salt buffers, especially at elevated temperature, can cause some conversion to relaxed form. A control reaction, including buffer and dnA but lacking enzyme, is incubated and run on the agarose gel fo Exonuclease Assay Suppliers use a variety of assays to check for exonuclease activ ity. a general assay mixture contains a restriction endonuclease 34 Robinson et al

Quality Control Assays—Maximum Units per Reaction When using procedures requiring larger quantities of enzyme and/or extended reaction times, an appreciation of the quality control data can help determine a safe amount of enzyme for your application. Overnight Assay Increasing amounts of restriction endonuclease are incubated overnight (typically for 16 hours) in their recommended buffer with 1mg of substrate DNA in a volume of 50ml. The characteris￾tic limit digest banding pattern produced by the enzyme in one hour is compared to the pattern produced from an excess of enzyme incubated overnight. A sharp, unaltered pattern under these conditions is an indication that the enzyme preparation is free of detectable levels of nonspecific endonucleases. The maximum number of units yielding an unaltered pattern is reported. Enzymes listing 100 units or more, a 1600-fold over digestion (100 units ¥ 16h), will not degrade DNA up to megabase size in mapping experiments and can be assumed to be virtually free of nonspecific endonuclease (Davis, T. and Robinson, D., unpublished observations). Nicking Assay Another sensitive test for contaminating endonucleases is a four hour incubation with a supercoiled plasmid that lacks a site for the enzyme being tested. The supercoil is very sensi￾tive to nonspecific nicking by a single-stranded endonuclease, cleavage by a double-stranded endonuclease, or topoisomerase activity. If a single-stranded nick occurs, the supercoiled mole￾cule, RFI, unwinds and assumes the circular form, RFII. If a double-stranded cleavage occurs, the circle will become linear. High levels of single-stranded nicking leads to linear DNA. All three forms of DNA have distinct electrophoretic mobilities on agarose gels. Enzymes converting 5% or less of the plasmid to relaxed form using 100 units of enzyme for four hours can be considered virtually free of nicking activity. High-salt buffers, especially at elevated temperature, can cause some conversion to relaxed form. A control reaction, including buffer and DNA but lacking enzyme, is incubated and run on the agarose gel for comparison. Exonuclease Assay Suppliers use a variety of assays to check for exonuclease activ￾ity. A general assay mixture contains a restriction endonuclease 234 Robinson et al